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Volumn 39, Issue 6, 2013, Pages 647-663

Gonadotropin-releasing hormone receptors as molecular therapeutic targets in prostate cancer: Current options and emerging strategies

Author keywords

Castration resistant; GnRH agonists; GnRH antagonists; GnRH receptors; GnRH based cytotoxic hybrids; GnRH II; GnRH III; Gonadotropin releasing hormone (GnRH); Prostate cancer; Targeted therapy

Indexed keywords

ABARELIX; CETRORELIX; D LYSINE GONDORELIN AGONIST; DEGARELIX; DESLORELIN; DESLORELIN DOCETAXEL BIOCONJUGATE; DOCETAXEL; FOLLITROPIN; GONADORELIN AGONIST; GONADORELIN RECEPTOR; GONADORELIN RECEPTOR II; GONADORELIN RECEPTOR III; GONADORELIN[6 DEXTRO LYSINE] 2 PYRROLINODOXORUBICIN; GOSERELIN; HISTRELIN; HORMONE RECEPTOR; LEUPRORELIN; LUTEINIZING HORMONE; OZARELIX; PREDNISONE; TESTOSTERONE; TRIPTORELIN; UNCLASSIFIED DRUG; ZOPTARELIN DOXORUBICIN;

EID: 84878921940     PISSN: 03057372     EISSN: 15321967     Source Type: Journal    
DOI: 10.1016/j.ctrv.2012.12.003     Document Type: Review
Times cited : (59)

References (257)
  • 2
    • 0036290334 scopus 로고    scopus 로고
    • Can combined androgen blockade provide long-term control or possible cure of localized prostate cancer?
    • Labrie F., Candas B., Gomez J.L., et al. Can combined androgen blockade provide long-term control or possible cure of localized prostate cancer?. Urology 2002, 60:115-119.
    • (2002) Urology , vol.60 , pp. 115-119
    • Labrie, F.1    Candas, B.2    Gomez, J.L.3
  • 4
    • 78650188152 scopus 로고    scopus 로고
    • Combined androgen blockade for prostate cancer: review of efficacy, safety and cost-effectiveness
    • Akaza H. Combined androgen blockade for prostate cancer: review of efficacy, safety and cost-effectiveness. Cancer Sci 2011, 102:51-56.
    • (2011) Cancer Sci , vol.102 , pp. 51-56
    • Akaza, H.1
  • 5
    • 68149098902 scopus 로고    scopus 로고
    • Combined androgen blockade with bicalutamide for advanced prostate cancer: long-term follow-up of a phase 3, double-blind, randomized study for survival
    • Akaza H., Hinotsu S., Usami M., et al. Combined androgen blockade with bicalutamide for advanced prostate cancer: long-term follow-up of a phase 3, double-blind, randomized study for survival. Cancer 2009, 115:3437-3445.
    • (2009) Cancer , vol.115 , pp. 3437-3445
    • Akaza, H.1    Hinotsu, S.2    Usami, M.3
  • 6
    • 2942739313 scopus 로고    scopus 로고
    • A re-assessment of the role of combined androgen blockade for advanced prostate cancer
    • Klotz L., Schellhammer P., Carroll K. A re-assessment of the role of combined androgen blockade for advanced prostate cancer. BJU Int 2004, 93:1177-1182.
    • (2004) BJU Int , vol.93 , pp. 1177-1182
    • Klotz, L.1    Schellhammer, P.2    Carroll, K.3
  • 7
    • 84863992416 scopus 로고    scopus 로고
    • Endocrine prevention and treatment of prostate cancer
    • Tammela T.L. Endocrine prevention and treatment of prostate cancer. Mol Cell Endocrinol 2012, 360:59-67.
    • (2012) Mol Cell Endocrinol , vol.360 , pp. 59-67
    • Tammela, T.L.1
  • 8
    • 33751581744 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone agonists in the treatment of prostate cancer: a review of their discovery, development, and place in therapy
    • Moreau J.P., Delavault P., Blumberg J. Luteinizing hormone-releasing hormone agonists in the treatment of prostate cancer: a review of their discovery, development, and place in therapy. Clin Ther 2006, 28:1485-1508.
    • (2006) Clin Ther , vol.28 , pp. 1485-1508
    • Moreau, J.P.1    Delavault, P.2    Blumberg, J.3
  • 9
    • 80755129141 scopus 로고    scopus 로고
    • Traditional approaches to androgen deprivation therapy
    • Moul J.W., Evans C.P., Gomella L.G., et al. Traditional approaches to androgen deprivation therapy. Urology 2011, 78:S485-S493.
    • (2011) Urology , vol.78
    • Moul, J.W.1    Evans, C.P.2    Gomella, L.G.3
  • 10
    • 84855284355 scopus 로고    scopus 로고
    • Efficacy and safety of gonadotropin-releasing hormone agonists used in the treatment of prostate cancer
    • Choi S., Lee A.K. Efficacy and safety of gonadotropin-releasing hormone agonists used in the treatment of prostate cancer. Drug Healthc Patient Saf 2011, 3:107-119.
    • (2011) Drug Healthc Patient Saf , vol.3 , pp. 107-119
    • Choi, S.1    Lee, A.K.2
  • 11
    • 1942437975 scopus 로고    scopus 로고
    • Medical castration with LHRH agonists: 25years later with major benefits achieved on survival in prostate cancer
    • Labrie F. Medical castration with LHRH agonists: 25years later with major benefits achieved on survival in prostate cancer. J Androl 2004, 25:305-313.
    • (2004) J Androl , vol.25 , pp. 305-313
    • Labrie, F.1
  • 12
    • 18844394827 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone agonists in the treatment of prostate cancer
    • Labrie F., Belanger A., Luu-The V., et al. Gonadotropin-releasing hormone agonists in the treatment of prostate cancer. Endocr Rev 2005, 26:361-379.
    • (2005) Endocr Rev , vol.26 , pp. 361-379
    • Labrie, F.1    Belanger, A.2    Luu-The, V.3
  • 13
    • 84862201613 scopus 로고    scopus 로고
    • Androgen deprivation therapy: past, present and future
    • Schroder F., Crawford E.D., Axcrona K., et al. Androgen deprivation therapy: past, present and future. BJU Int 2012, 109(Suppl 6):1-12.
    • (2012) BJU Int , vol.109 , Issue.SUPPL. 6 , pp. 1-12
    • Schroder, F.1    Crawford, E.D.2    Axcrona, K.3
  • 14
    • 77951445053 scopus 로고    scopus 로고
    • Update on castrate-resistant prostate cancer: 2010
    • Lassi K., Dawson N.A. Update on castrate-resistant prostate cancer: 2010. Curr Opin Oncol 2010, 22:263-267.
    • (2010) Curr Opin Oncol , vol.22 , pp. 263-267
    • Lassi, K.1    Dawson, N.A.2
  • 15
    • 84863822661 scopus 로고    scopus 로고
    • Life after failure of traditional androgen deprivation therapy
    • Schellhammer P. Life after failure of traditional androgen deprivation therapy. Urol Oncol 2012, 30:S10-14.
    • (2012) Urol Oncol , vol.30
    • Schellhammer, P.1
  • 16
    • 58149302446 scopus 로고    scopus 로고
    • Progression of prostate cancer: multiple pathways to androgen independence
    • Devlin H.L., Mudryj M. Progression of prostate cancer: multiple pathways to androgen independence. Cancer Lett 2009, 274:177-186.
    • (2009) Cancer Lett , vol.274 , pp. 177-186
    • Devlin, H.L.1    Mudryj, M.2
  • 17
    • 69249203584 scopus 로고    scopus 로고
    • Castration-resistant prostate cancer: from new pathophysiology to new treatment targets
    • Chi K.N., Bjartell A., Dearnaley D., et al. Castration-resistant prostate cancer: from new pathophysiology to new treatment targets. Eur Urol 2009, 56:594-605.
    • (2009) Eur Urol , vol.56 , pp. 594-605
    • Chi, K.N.1    Bjartell, A.2    Dearnaley, D.3
  • 18
    • 8944220720 scopus 로고    scopus 로고
    • Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points
    • Tannock I.F., Osoba D., Stockler M.R., et al. Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points. J Clin Oncol 1996, 14:1756-1764.
    • (1996) J Clin Oncol , vol.14 , pp. 1756-1764
    • Tannock, I.F.1    Osoba, D.2    Stockler, M.R.3
  • 19
    • 4744337716 scopus 로고    scopus 로고
    • Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer
    • Petrylak D.P., Tangen C.M., Hussain M.H., et al. Docetaxel and estramustine compared with mitoxantrone and prednisone for advanced refractory prostate cancer. N Engl J Med 2004, 351:1513-1520.
    • (2004) N Engl J Med , vol.351 , pp. 1513-1520
    • Petrylak, D.P.1    Tangen, C.M.2    Hussain, M.H.3
  • 20
    • 57649213265 scopus 로고    scopus 로고
    • The role of systemic cytotoxic therapy for prostate cancer
    • Chang S.S., Kibel A.S. The role of systemic cytotoxic therapy for prostate cancer. BJU Int 2009, 103:8-17.
    • (2009) BJU Int , vol.103 , pp. 8-17
    • Chang, S.S.1    Kibel, A.S.2
  • 21
    • 77952427224 scopus 로고    scopus 로고
    • Molecular and traditional chemotherapy: a united front against prostate cancer
    • Singh P., Yam M., Russell P.J., et al. Molecular and traditional chemotherapy: a united front against prostate cancer. Cancer Lett 2010, 293:1-14.
    • (2010) Cancer Lett , vol.293 , pp. 1-14
    • Singh, P.1    Yam, M.2    Russell, P.J.3
  • 22
    • 62649133923 scopus 로고    scopus 로고
    • Mechanisms of prostate cancer cell survival after inhibition of AR expression
    • Cohen M.B., Rokhlin O.W. Mechanisms of prostate cancer cell survival after inhibition of AR expression. J Cell Biochem 2009, 106:363-371.
    • (2009) J Cell Biochem , vol.106 , pp. 363-371
    • Cohen, M.B.1    Rokhlin, O.W.2
  • 23
    • 79953320228 scopus 로고    scopus 로고
    • New strategies in metastatic prostate cancer: targeting the androgen receptor signaling pathway
    • Attard G., Richards J., de Bono J.S. New strategies in metastatic prostate cancer: targeting the androgen receptor signaling pathway. Clin Cancer Res 2011, 17:1649-1657.
    • (2011) Clin Cancer Res , vol.17 , pp. 1649-1657
    • Attard, G.1    Richards, J.2    de Bono, J.S.3
  • 24
    • 84859425018 scopus 로고    scopus 로고
    • Novel molecular targets for the therapy of castration-resistant prostate cancer
    • Agarwal N., Sonpavde G., Sternberg C.N. Novel molecular targets for the therapy of castration-resistant prostate cancer. Eur Urol 2012, 61:950-960.
    • (2012) Eur Urol , vol.61 , pp. 950-960
    • Agarwal, N.1    Sonpavde, G.2    Sternberg, C.N.3
  • 25
    • 84874425541 scopus 로고    scopus 로고
    • A changing landscape in castration-resistant prostate cancer treatment
    • Felici A., Pino M.S., Carlini P. A changing landscape in castration-resistant prostate cancer treatment. Front Endocrinol 2012, 3:1-8.
    • (2012) Front Endocrinol , vol.3 , pp. 1-8
    • Felici, A.1    Pino, M.S.2    Carlini, P.3
  • 26
    • 80052527251 scopus 로고    scopus 로고
    • Management of metastatic castration-resistant prostate cancer after first-line docetaxel
    • Harrington J.A., Jones R.J. Management of metastatic castration-resistant prostate cancer after first-line docetaxel. Eur J Cancer 2011, 47:2133-2142.
    • (2011) Eur J Cancer , vol.47 , pp. 2133-2142
    • Harrington, J.A.1    Jones, R.J.2
  • 27
    • 79959194682 scopus 로고    scopus 로고
    • Overcoming chemotherapy resistance in prostate cancer
    • Madan R.A., Pal S.K., Sartor O., et al. Overcoming chemotherapy resistance in prostate cancer. Clin Cancer Res 2011, 17:3892-3902.
    • (2011) Clin Cancer Res , vol.17 , pp. 3892-3902
    • Madan, R.A.1    Pal, S.K.2    Sartor, O.3
  • 28
    • 77949875831 scopus 로고    scopus 로고
    • Novel targeted therapeutics for metastatic castration-resistant prostate cancer
    • Antonarakis E.S., Carducci M.A., Eisenberger M.A. Novel targeted therapeutics for metastatic castration-resistant prostate cancer. Cancer Lett 2010, 291:1-13.
    • (2010) Cancer Lett , vol.291 , pp. 1-13
    • Antonarakis, E.S.1    Carducci, M.A.2    Eisenberger, M.A.3
  • 29
    • 79851510026 scopus 로고    scopus 로고
    • Novel therapeutic strategies for castration resistant prostate cancer: inhibition of persistent androgen production and androgen receptor mediated signaling
    • Molina A., Belldegrun A. Novel therapeutic strategies for castration resistant prostate cancer: inhibition of persistent androgen production and androgen receptor mediated signaling. J Urol 2011, 185:787-794.
    • (2011) J Urol , vol.185 , pp. 787-794
    • Molina, A.1    Belldegrun, A.2
  • 30
    • 84856054939 scopus 로고    scopus 로고
    • Emerging novel therapies for advanced prostate cancer
    • Osanto S., Van Poppel H. Emerging novel therapies for advanced prostate cancer. Ther Adv Urol 2012, 4:3-12.
    • (2012) Ther Adv Urol , vol.4 , pp. 3-12
    • Osanto, S.1    Van Poppel, H.2
  • 31
    • 84865336863 scopus 로고    scopus 로고
    • Optimizing the care of patients with advanced prostate cancer in the UK: current challenges and future opportunities
    • Payne H., Bahl A., Mason M., et al. Optimizing the care of patients with advanced prostate cancer in the UK: current challenges and future opportunities. BJU Int 2012, 110:658-667.
    • (2012) BJU Int , vol.110 , pp. 658-667
    • Payne, H.1    Bahl, A.2    Mason, M.3
  • 32
    • 77956667524 scopus 로고    scopus 로고
    • Expression of receptors for luteinizing hormone-releasing hormone (LH-RH) in prostate cancers following therapy with LH-RH agonists
    • Liu S.V., Schally A.V., Hawes D., et al. Expression of receptors for luteinizing hormone-releasing hormone (LH-RH) in prostate cancers following therapy with LH-RH agonists. Clin Cancer Res 2010, 16:4675-4680.
    • (2010) Clin Cancer Res , vol.16 , pp. 4675-4680
    • Liu, S.V.1    Schally, A.V.2    Hawes, D.3
  • 33
    • 0015228709 scopus 로고
    • Isolation and properties of the FSH and LH-releasing hormone
    • Schally A.V., Arimura A., Baba Y., et al. Isolation and properties of the FSH and LH-releasing hormone. Biochem Biophys Res Commun 1971, 43:393-399.
    • (1971) Biochem Biophys Res Commun , vol.43 , pp. 393-399
    • Schally, A.V.1    Arimura, A.2    Baba, Y.3
  • 34
    • 0028306250 scopus 로고
    • Gonadotropin-releasing hormone and its analogs
    • Conn P.M., Crowley W.F. Gonadotropin-releasing hormone and its analogs. Annu Rev Med 1994, 45:391-405.
    • (1994) Annu Rev Med , vol.45 , pp. 391-405
    • Conn, P.M.1    Crowley, W.F.2
  • 35
    • 17044397637 scopus 로고    scopus 로고
    • Molecular biology of gonadotropin-releasing hormone (GnRH)-I, GnRH-II, and their receptors in humans
    • Cheng C.K., Leung P.C. Molecular biology of gonadotropin-releasing hormone (GnRH)-I, GnRH-II, and their receptors in humans. Endocr Rev 2005, 26:283-306.
    • (2005) Endocr Rev , vol.26 , pp. 283-306
    • Cheng, C.K.1    Leung, P.C.2
  • 36
    • 24044447902 scopus 로고    scopus 로고
    • GnRHs and GnRH receptors
    • Millar R.P. GnRHs and GnRH receptors. Anim Reprod Sci 2005, 88:5-28.
    • (2005) Anim Reprod Sci , vol.88 , pp. 5-28
    • Millar, R.P.1
  • 37
    • 11244260381 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone and its receptor in normal and malignant cells
    • Harrison G.S., Wierman M.E., Nett T.M., et al. Gonadotropin-releasing hormone and its receptor in normal and malignant cells. Endocr Relat Cancer 2004, 11:725-748.
    • (2004) Endocr Relat Cancer , vol.11 , pp. 725-748
    • Harrison, G.S.1    Wierman, M.E.2    Nett, T.M.3
  • 38
    • 84870839178 scopus 로고    scopus 로고
    • GnRH receptors in cancer: from cell biology to novel targeted therapeutic strategies
    • Limonta P., Montagnani Marelli M., Mai S. GnRH receptors in cancer: from cell biology to novel targeted therapeutic strategies. Endocr Rev 2012, 33:784-811.
    • (2012) Endocr Rev , vol.33 , pp. 784-811
    • Limonta, P.1    Montagnani Marelli, M.2    Mai, S.3
  • 39
    • 0025836522 scopus 로고
    • Computer-assisted mapping of immunoreactive mammalian gonadotropin-releasing hormone in adult human basal forebrain and amygdala
    • Stopa E.G., Koh E.T., Svendsen C.N., et al. Computer-assisted mapping of immunoreactive mammalian gonadotropin-releasing hormone in adult human basal forebrain and amygdala. Endocrinology 1991, 128:3199-3207.
    • (1991) Endocrinology , vol.128 , pp. 3199-3207
    • Stopa, E.G.1    Koh, E.T.2    Svendsen, C.N.3
  • 40
    • 0023065849 scopus 로고
    • The mammalian GnRH gene and its pivotal role in reproduction
    • Seeburg P.H., Mason A.J., Stewart T.A., et al. The mammalian GnRH gene and its pivotal role in reproduction. Recent Prog Horm Res 1987, 43:69-98.
    • (1987) Recent Prog Horm Res , vol.43 , pp. 69-98
    • Seeburg, P.H.1    Mason, A.J.2    Stewart, T.A.3
  • 41
    • 0024334456 scopus 로고
    • The complete nucleotide sequence of the human gonadotropin-releasing hormone gene
    • Hayflick J.S., Adelman J.P., Seeburg P.H. The complete nucleotide sequence of the human gonadotropin-releasing hormone gene. Nucleic Acids Res 1989, 17:6403-6404.
    • (1989) Nucleic Acids Res , vol.17 , pp. 6403-6404
    • Hayflick, J.S.1    Adelman, J.P.2    Seeburg, P.H.3
  • 42
    • 0025319890 scopus 로고
    • Isolation and characterization of the human gonadotropin-releasing hormone gene in the hypothalamus and placenta
    • Radovick S., Wondisford F.E., Nakayama Y., et al. Isolation and characterization of the human gonadotropin-releasing hormone gene in the hypothalamus and placenta. Mol Endocrinol 1990, 4:476-480.
    • (1990) Mol Endocrinol , vol.4 , pp. 476-480
    • Radovick, S.1    Wondisford, F.E.2    Nakayama, Y.3
  • 43
    • 3843131055 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptors
    • Millar R.P., Lu Z.L., Pawson A.J., et al. Gonadotropin-releasing hormone receptors. Endocr Rev 2004, 25:235-275.
    • (2004) Endocr Rev , vol.25 , pp. 235-275
    • Millar, R.P.1    Lu, Z.L.2    Pawson, A.J.3
  • 44
    • 85047684264 scopus 로고    scopus 로고
    • GnRH and GnRH receptor genes in the human genome
    • Neill J.D. GnRH and GnRH receptor genes in the human genome. Endocrinology 2002, 143:737-743.
    • (2002) Endocrinology , vol.143 , pp. 737-743
    • Neill, J.D.1
  • 45
    • 0028092770 scopus 로고
    • Gonadotropin-releasing hormone receptors: structure and signal transduction pathways
    • Stojilkovic S.S., Reinhart J., Catt K.J. Gonadotropin-releasing hormone receptors: structure and signal transduction pathways. Endocr Rev 1994, 15:462-499.
    • (1994) Endocr Rev , vol.15 , pp. 462-499
    • Stojilkovic, S.S.1    Reinhart, J.2    Catt, K.J.3
  • 46
    • 4143134065 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptors: structure, expression, and signaling transduction
    • Kakar S.S., Malik M.T., Winters S.J., et al. Gonadotropin-releasing hormone receptors: structure, expression, and signaling transduction. Vitam Horm 2004, 69:151-207.
    • (2004) Vitam Horm , vol.69 , pp. 151-207
    • Kakar, S.S.1    Malik, M.T.2    Winters, S.J.3
  • 47
    • 0027051673 scopus 로고
    • Cloning, sequencing, and expression of human gonadotropin releasing hormone (GnRH) receptor
    • Kakar S.S., Musgrove L.C., Devor D.C., et al. Cloning, sequencing, and expression of human gonadotropin releasing hormone (GnRH) receptor. Biochem Biophys Res Commun 1992, 189:289-295.
    • (1992) Biochem Biophys Res Commun , vol.189 , pp. 289-295
    • Kakar, S.S.1    Musgrove, L.C.2    Devor, D.C.3
  • 48
    • 24044509155 scopus 로고    scopus 로고
    • Pituitary gonadotropin-releasing hormone (GnRH) receptor: structure, distribution and regulation of expression
    • Rispoli L.A., Nett T.M. Pituitary gonadotropin-releasing hormone (GnRH) receptor: structure, distribution and regulation of expression. Anim Reprod Sci 2005, 88:57-74.
    • (2005) Anim Reprod Sci , vol.88 , pp. 57-74
    • Rispoli, L.A.1    Nett, T.M.2
  • 49
    • 0028234277 scopus 로고
    • The human gonadotropin-releasing hormone (GnRH) receptor gene: cloning, genomic organization and chromosomal assignment
    • Fan N.C., Jeung E.B., Peng C., et al. The human gonadotropin-releasing hormone (GnRH) receptor gene: cloning, genomic organization and chromosomal assignment. Mol Cell Endocrinol 1994, 103:R1-6.
    • (1994) Mol Cell Endocrinol , vol.103
    • Fan, N.C.1    Jeung, E.B.2    Peng, C.3
  • 50
    • 0031038565 scopus 로고    scopus 로고
    • Studies of gonadotropin-releasing hormone (GnRH) action using GnRH receptor-expressing pituitary cell lines
    • Kaiser U.B., Conn P.M., Chin W.W. Studies of gonadotropin-releasing hormone (GnRH) action using GnRH receptor-expressing pituitary cell lines. Endocr Rev 1997, 18:46-70.
    • (1997) Endocr Rev , vol.18 , pp. 46-70
    • Kaiser, U.B.1    Conn, P.M.2    Chin, W.W.3
  • 51
    • 0028242680 scopus 로고
    • Absence of rapid desensitization of the mouse gonadotropin-releasing hormone receptor
    • Davidson J.S., Wakefield I.K., Millar R.P. Absence of rapid desensitization of the mouse gonadotropin-releasing hormone receptor. Biochem J 1994, 300(Pt 2):299-302.
    • (1994) Biochem J , vol.300 , Issue.PART 2 , pp. 299-302
    • Davidson, J.S.1    Wakefield, I.K.2    Millar, R.P.3
  • 52
    • 17744382379 scopus 로고    scopus 로고
    • Desensitization and internalization of human and xenopus gonadotropin-releasing hormone receptors expressed in alphaT4 pituitary cells using recombinant adenovirus
    • Hislop J.N., Madziva M.T., Everest H.M., et al. Desensitization and internalization of human and xenopus gonadotropin-releasing hormone receptors expressed in alphaT4 pituitary cells using recombinant adenovirus. Endocrinology 2000, 141:4564-4575.
    • (2000) Endocrinology , vol.141 , pp. 4564-4575
    • Hislop, J.N.1    Madziva, M.T.2    Everest, H.M.3
  • 53
    • 0036241442 scopus 로고    scopus 로고
    • Signalling, cycling and desensitisation of gonadotrophin-releasing hormone receptors
    • McArdle C.A., Franklin J., Green L., et al. Signalling, cycling and desensitisation of gonadotrophin-releasing hormone receptors. J Endocrinol 2002, 173:1-11.
    • (2002) J Endocrinol , vol.173 , pp. 1-11
    • McArdle, C.A.1    Franklin, J.2    Green, L.3
  • 54
    • 0035676783 scopus 로고    scopus 로고
    • Intracellular signaling pathways mediated by the gonadotropin-releasing hormone (GnRH) receptor
    • Kraus S., Naor Z., Seger R. Intracellular signaling pathways mediated by the gonadotropin-releasing hormone (GnRH) receptor. Arch Med Res 2001, 32:499-509.
    • (2001) Arch Med Res , vol.32 , pp. 499-509
    • Kraus, S.1    Naor, Z.2    Seger, R.3
  • 55
    • 0142227708 scopus 로고    scopus 로고
    • Structure of the GnRH receptor-stimulated signaling network: insights from genomics
    • Ruf F., Fink M.Y., Sealfon S.C. Structure of the GnRH receptor-stimulated signaling network: insights from genomics. Front Neuroendocrinol 2003, 24:181-199.
    • (2003) Front Neuroendocrinol , vol.24 , pp. 181-199
    • Ruf, F.1    Fink, M.Y.2    Sealfon, S.C.3
  • 56
    • 58049165874 scopus 로고    scopus 로고
    • Signaling by G-protein-coupled receptor (GPCR): studies on the GnRH receptor
    • Naor Z. Signaling by G-protein-coupled receptor (GPCR): studies on the GnRH receptor. Front Neuroendocrinol 2009, 30:10-29.
    • (2009) Front Neuroendocrinol , vol.30 , pp. 10-29
    • Naor, Z.1
  • 57
    • 84862904885 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptor signaling: biased and unbiased
    • McArdle C.A. Gonadotropin-releasing hormone receptor signaling: biased and unbiased. Mini Rev Med Chem 2012, 12:841-850.
    • (2012) Mini Rev Med Chem , vol.12 , pp. 841-850
    • McArdle, C.A.1
  • 58
    • 77956580208 scopus 로고    scopus 로고
    • The long-term clinical follow-up and natural history of men with adult-onset idiopathic hypogonadotropic hypogonadism
    • Dwyer A.A., Hayes F.J., Plummer L., et al. The long-term clinical follow-up and natural history of men with adult-onset idiopathic hypogonadotropic hypogonadism. J Clin Endocrinol Metab 2010, 95:4235-4243.
    • (2010) J Clin Endocrinol Metab , vol.95 , pp. 4235-4243
    • Dwyer, A.A.1    Hayes, F.J.2    Plummer, L.3
  • 59
    • 77952641591 scopus 로고    scopus 로고
    • What is the optimal therapy for young males with hypogonadotropic hypogonadism?
    • Han T.S., Bouloux P.M. What is the optimal therapy for young males with hypogonadotropic hypogonadism?. Clin Endocrinol (Oxf) 2010, 72:731-737.
    • (2010) Clin Endocrinol (Oxf) , vol.72 , pp. 731-737
    • Han, T.S.1    Bouloux, P.M.2
  • 60
    • 0028235123 scopus 로고
    • The use of luteinizing hormone releasing hormone agonists and antagonists in gynaecological cancers
    • Emons G., Schally A.V. The use of luteinizing hormone releasing hormone agonists and antagonists in gynaecological cancers. Hum Reprod 1994, 9:1364-1379.
    • (1994) Hum Reprod , vol.9 , pp. 1364-1379
    • Emons, G.1    Schally, A.V.2
  • 61
    • 80055092441 scopus 로고    scopus 로고
    • Gonadotrophin-releasing hormone agonist protocols for pituitary suppression in assisted reproduction
    • Maheshwari A., Gibreel A., Siristatidis C.S., et al. Gonadotrophin-releasing hormone agonist protocols for pituitary suppression in assisted reproduction. Cochrane Database Syst Rev 2011, CD006919.
    • (2011) Cochrane Database Syst Rev
    • Maheshwari, A.1    Gibreel, A.2    Siristatidis, C.S.3
  • 62
    • 84863792976 scopus 로고    scopus 로고
    • Gonadotropin releasing hormone agonists: expanding vistas
    • Magon N. Gonadotropin releasing hormone agonists: expanding vistas. Indian J Endocrinol Metab 2011, 15:261-267.
    • (2011) Indian J Endocrinol Metab , vol.15 , pp. 261-267
    • Magon, N.1
  • 64
    • 0344444706 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone antagonists
    • Herbst K.L. Gonadotropin-releasing hormone antagonists. Curr Opin Pharmacol 2003, 3:660-666.
    • (2003) Curr Opin Pharmacol , vol.3 , pp. 660-666
    • Herbst, K.L.1
  • 66
    • 42949178706 scopus 로고    scopus 로고
    • Are GnRH antagonists comparable to agonists for use in IVF?
    • Huirne J.A., Homburg R., Lambalk C.B. Are GnRH antagonists comparable to agonists for use in IVF?. Hum Reprod 2007, 22:2805-2813.
    • (2007) Hum Reprod , vol.22 , pp. 2805-2813
    • Huirne, J.A.1    Homburg, R.2    Lambalk, C.B.3
  • 67
    • 0347320615 scopus 로고    scopus 로고
    • The biology of gonadotropin hormone-releasing hormone: role in the control of tumor growth and progression in humans
    • Limonta P., Moretti R.M., Marelli M.M., et al. The biology of gonadotropin hormone-releasing hormone: role in the control of tumor growth and progression in humans. Front Neuroendocrinol 2003, 24:279-295.
    • (2003) Front Neuroendocrinol , vol.24 , pp. 279-295
    • Limonta, P.1    Moretti, R.M.2    Marelli, M.M.3
  • 68
    • 33646878065 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone (GnRH) receptors in tumors: a new rationale for the therapeutical application of GnRH analogs in cancer patients?
    • Marelli M.M., Moretti R.M., Januszkiewicz-Caulier J., et al. Gonadotropin-releasing hormone (GnRH) receptors in tumors: a new rationale for the therapeutical application of GnRH analogs in cancer patients?. Curr Cancer Drug Targets 2006, 6:257-269.
    • (2006) Curr Cancer Drug Targets , vol.6 , pp. 257-269
    • Marelli, M.M.1    Moretti, R.M.2    Januszkiewicz-Caulier, J.3
  • 69
    • 0035066873 scopus 로고    scopus 로고
    • Montagnani Marelli M, Moretti RM, LHRH analogues as anticancer agents: pituitary and extrapituitary sites of action
    • Limonta P. Montagnani Marelli M, Moretti RM, LHRH analogues as anticancer agents: pituitary and extrapituitary sites of action. Expert Opin Investig Drugs 2001, 10:709-720.
    • (2001) Expert Opin Investig Drugs , vol.10 , pp. 709-720
    • Limonta, P.1
  • 71
    • 0034616656 scopus 로고    scopus 로고
    • Combined treatment with buserelin and tamoxifen in premenopausal metastatic breast cancer: a randomized study
    • Klijn J.G., Beex L.V., Mauriac L., et al. Combined treatment with buserelin and tamoxifen in premenopausal metastatic breast cancer: a randomized study. J Natl Cancer Inst 2000, 92:903-911.
    • (2000) J Natl Cancer Inst , vol.92 , pp. 903-911
    • Klijn, J.G.1    Beex, L.V.2    Mauriac, L.3
  • 72
    • 10144237848 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone agonist triptorelin in combination with cytotoxic chemotherapy in patients with advanced ovarian carcinoma. A prospective double blind randomized trial. Decapeptyl Ovarian Cancer Study Group
    • Emons G., Ortmann O., Teichert H.M., et al. Luteinizing hormone-releasing hormone agonist triptorelin in combination with cytotoxic chemotherapy in patients with advanced ovarian carcinoma. A prospective double blind randomized trial. Decapeptyl Ovarian Cancer Study Group. Cancer 1996, 78:1452-1460.
    • (1996) Cancer , vol.78 , pp. 1452-1460
    • Emons, G.1    Ortmann, O.2    Teichert, H.M.3
  • 73
    • 33846414318 scopus 로고    scopus 로고
    • Drug Insight: clinical use of agonists and antagonists of luteinizing-hormone-releasing hormone
    • Engel J.B., Schally A.V. Drug Insight: clinical use of agonists and antagonists of luteinizing-hormone-releasing hormone. Nat Clin Pract Endocrinol Metab 2007, 3:157-167.
    • (2007) Nat Clin Pract Endocrinol Metab , vol.3 , pp. 157-167
    • Engel, J.B.1    Schally, A.V.2
  • 74
    • 4344637399 scopus 로고    scopus 로고
    • Role of gonadotropin-releasing hormone (GnRH) in ovarian cancer
    • Grundker C., Emons G. Role of gonadotropin-releasing hormone (GnRH) in ovarian cancer. Reprod Biol Endocrinol 2003, 1:65.
    • (2003) Reprod Biol Endocrinol , vol.1 , pp. 65
    • Grundker, C.1    Emons, G.2
  • 75
    • 0036164170 scopus 로고    scopus 로고
    • Biology of the gonadotropin-releasing hormone system in gynecological cancers
    • Grundker C., Gunthert A.R., Westphalen S., et al. Biology of the gonadotropin-releasing hormone system in gynecological cancers. Eur J Endocrinol 2002, 146:1-14.
    • (2002) Eur J Endocrinol , vol.146 , pp. 1-14
    • Grundker, C.1    Gunthert, A.R.2    Westphalen, S.3
  • 76
    • 73649137902 scopus 로고    scopus 로고
    • Receptor-mediated tumor targeting based on peptide hormones
    • Mezo G., Manea M. Receptor-mediated tumor targeting based on peptide hormones. Expert Opin Drug Deliv 2010, 7:79-96.
    • (2010) Expert Opin Drug Deliv , vol.7 , pp. 79-96
    • Mezo, G.1    Manea, M.2
  • 77
    • 55249123112 scopus 로고    scopus 로고
    • New derivatives of GnRH as potential anticancer therapeutic agents
    • Mezo G., Manea M., Szabi I., et al. New derivatives of GnRH as potential anticancer therapeutic agents. Curr Med Chem 2008, 15:2366-2379.
    • (2008) Curr Med Chem , vol.15 , pp. 2366-2379
    • Mezo, G.1    Manea, M.2    Szabi, I.3
  • 78
    • 0018862628 scopus 로고
    • Comparative aspects of luteinizing hormone-releasing hormone structure and function in vertebrate phylogeny
    • King J.A., Millar R.P. Comparative aspects of luteinizing hormone-releasing hormone structure and function in vertebrate phylogeny. Endocrinology 1980, 106:707-717.
    • (1980) Endocrinology , vol.106 , pp. 707-717
    • King, J.A.1    Millar, R.P.2
  • 79
    • 0032544747 scopus 로고    scopus 로고
    • A second isoform of gonadotropin-releasing hormone is present in the brain of human and rodents
    • Chen A., Yahalom D., Ben-Aroya N., et al. A second isoform of gonadotropin-releasing hormone is present in the brain of human and rodents. FEBS Lett 1998, 435:199-203.
    • (1998) FEBS Lett , vol.435 , pp. 199-203
    • Chen, A.1    Yahalom, D.2    Ben-Aroya, N.3
  • 80
    • 0031889781 scopus 로고    scopus 로고
    • Second gene for gonadotropin-releasing hormone in humans
    • White R.B., Eisen J.A., Kasten T.L., et al. Second gene for gonadotropin-releasing hormone in humans. Proc Natl Acad Sci USA 1998, 95:305-309.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 305-309
    • White, R.B.1    Eisen, J.A.2    Kasten, T.L.3
  • 81
    • 0035114414 scopus 로고    scopus 로고
    • Differential regulation of two forms of gonadotropin-releasing hormone messenger ribonucleic acid in human granulosa-luteal cells
    • Kang S.K., Tai C.J., Nathwani P.S., et al. Differential regulation of two forms of gonadotropin-releasing hormone messenger ribonucleic acid in human granulosa-luteal cells. Endocrinology 2001, 142:182-192.
    • (2001) Endocrinology , vol.142 , pp. 182-192
    • Kang, S.K.1    Tai, C.J.2    Nathwani, P.S.3
  • 82
    • 0038627514 scopus 로고    scopus 로고
    • Multi-factorial role of GnRH-I and GnRH-II in the human ovary
    • Leung P.C., Cheng C.K., Zhu X.M. Multi-factorial role of GnRH-I and GnRH-II in the human ovary. Mol Cell Endocrinol 2003, 202:145-153.
    • (2003) Mol Cell Endocrinol , vol.202 , pp. 145-153
    • Leung, P.C.1    Cheng, C.K.2    Zhu, X.M.3
  • 83
    • 4744346569 scopus 로고    scopus 로고
    • Emerging functions of gonadotropin-releasing hormone II in mammalian physiology and behaviour
    • Kauffman A.S. Emerging functions of gonadotropin-releasing hormone II in mammalian physiology and behaviour. J Neuroendocrinol 2004, 16:794-806.
    • (2004) J Neuroendocrinol , vol.16 , pp. 794-806
    • Kauffman, A.S.1
  • 84
    • 0141613856 scopus 로고    scopus 로고
    • Type II gonadotrophin-releasing hormone (GnRH-II) in reproductive biology
    • Pawson A.J., Morgan K., Maudsley S.R., et al. Type II gonadotrophin-releasing hormone (GnRH-II) in reproductive biology. Reproduction 2003, 126:271-278.
    • (2003) Reproduction , vol.126 , pp. 271-278
    • Pawson, A.J.1    Morgan, K.2    Maudsley, S.R.3
  • 85
    • 0035004022 scopus 로고    scopus 로고
    • Expression of the second isoform of gonadotrophin-releasing hormone (GnRH-II) in human endometrium throughout the menstrual cycle
    • Cheon K.W., Lee H.S., Parhar I.S., et al. Expression of the second isoform of gonadotrophin-releasing hormone (GnRH-II) in human endometrium throughout the menstrual cycle. Mol Hum Reprod 2001, 7:447-452.
    • (2001) Mol Hum Reprod , vol.7 , pp. 447-452
    • Cheon, K.W.1    Lee, H.S.2    Parhar, I.S.3
  • 86
    • 0034810482 scopus 로고    scopus 로고
    • A gonadotropin-releasing hormone (GnRH) receptor specific for GnRH II in primates
    • Neill J.D., Duck L.W., Sellers J.C., et al. A gonadotropin-releasing hormone (GnRH) receptor specific for GnRH II in primates. Biochem Biophys Res Commun 2001, 282:1012-1018.
    • (2001) Biochem Biophys Res Commun , vol.282 , pp. 1012-1018
    • Neill, J.D.1    Duck, L.W.2    Sellers, J.C.3
  • 87
    • 0035859957 scopus 로고    scopus 로고
    • A novel mammalian receptor for the evolutionarily conserved type II GnRH
    • Millar R., Lowe S., Conklin D., et al. A novel mammalian receptor for the evolutionarily conserved type II GnRH. Proc Natl Acad Sci USA 2001, 98:9636-9641.
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 9636-9641
    • Millar, R.1    Lowe, S.2    Conklin, D.3
  • 88
    • 4544262511 scopus 로고    scopus 로고
    • Newly recognized GnRH receptors: function and relative role
    • Neill J.D., Musgrove L.C., Duck L.W. Newly recognized GnRH receptors: function and relative role. Trends Endocrinol Metab 2004, 15:383-392.
    • (2004) Trends Endocrinol Metab , vol.15 , pp. 383-392
    • Neill, J.D.1    Musgrove, L.C.2    Duck, L.W.3
  • 89
    • 0034756120 scopus 로고    scopus 로고
    • The genes encoding the type II gonadotropin-releasing hormone receptor and the ribonucleoprotein RBM8A in humans overlap in two genomic loci
    • Faurholm B., Millar R.P., Katz A.A. The genes encoding the type II gonadotropin-releasing hormone receptor and the ribonucleoprotein RBM8A in humans overlap in two genomic loci. Genomics 2001, 78:15-18.
    • (2001) Genomics , vol.78 , pp. 15-18
    • Faurholm, B.1    Millar, R.P.2    Katz, A.A.3
  • 90
    • 0036965115 scopus 로고    scopus 로고
    • Expression of gonadotropin-releasing hormone II (GnRH-II) receptor in human endometrial and ovarian cancer cells and effects of GnRH-II on tumor cell proliferation
    • Grundker C., Gunthert A.R., Millar R.P., et al. Expression of gonadotropin-releasing hormone II (GnRH-II) receptor in human endometrial and ovarian cancer cells and effects of GnRH-II on tumor cell proliferation. J Clin Endocrinol Metab 2002, 87:1427-1430.
    • (2002) J Clin Endocrinol Metab , vol.87 , pp. 1427-1430
    • Grundker, C.1    Gunthert, A.R.2    Millar, R.P.3
  • 91
    • 2942685557 scopus 로고    scopus 로고
    • Type II gonadotropin-releasing hormone stimulates p38 mitogen-activated protein kinase and apoptosis in ovarian cancer cells
    • Kim K.Y., Choi K.C., Park S.H., et al. Type II gonadotropin-releasing hormone stimulates p38 mitogen-activated protein kinase and apoptosis in ovarian cancer cells. J Clin Endocrinol Metab 2004, 893020-893026.
    • (2004) J Clin Endocrinol Metab , pp. 893020-893026
    • Kim, K.Y.1    Choi, K.C.2    Park, S.H.3
  • 92
    • 27644458748 scopus 로고    scopus 로고
    • Analogs of GnRH-I and GnRH-II inhibit epidermal growth factor-induced signal transduction and resensitize resistant human breast cancer cells to 4OH-tamoxifen
    • Gunthert A.R., Grundker C., Olota A., et al. Analogs of GnRH-I and GnRH-II inhibit epidermal growth factor-induced signal transduction and resensitize resistant human breast cancer cells to 4OH-tamoxifen. Eur J Endocrinol 2005, 153:613-625.
    • (2005) Eur J Endocrinol , vol.153 , pp. 613-625
    • Gunthert, A.R.1    Grundker, C.2    Olota, A.3
  • 93
    • 66149107972 scopus 로고    scopus 로고
    • Type I gonadotropin-releasing hormone receptor mediates the antiproliferative effects of GnRH-II on prostate cancer cells
    • Montagnani Marelli M., Moretti R.M., Mai S., et al. Type I gonadotropin-releasing hormone receptor mediates the antiproliferative effects of GnRH-II on prostate cancer cells. J Clin Endocrinol Metab 2009, 94:1761-1767.
    • (2009) J Clin Endocrinol Metab , vol.94 , pp. 1761-1767
    • Montagnani Marelli, M.1    Moretti, R.M.2    Mai, S.3
  • 94
    • 70049086395 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone (GnRH)-I and GnRH-II induce cell growth inhibition in human endometrial cancer cells: involvement of integrin beta3 and focal adhesion kinase
    • Park D.W., Choi K.C., MacCalman C.D., et al. Gonadotropin-releasing hormone (GnRH)-I and GnRH-II induce cell growth inhibition in human endometrial cancer cells: involvement of integrin beta3 and focal adhesion kinase. Reprod Biol Endocrinol 2009, 7:81.
    • (2009) Reprod Biol Endocrinol , vol.7 , pp. 81
    • Park, D.W.1    Choi, K.C.2    MacCalman, C.D.3
  • 95
    • 15944401007 scopus 로고    scopus 로고
    • Extracellular signal-regulated protein kinase, but not c-Jun N-terminal kinase, is activated by type II gonadotropin-releasing hormone involved in the inhibition of ovarian cancer cell proliferation
    • Kim K.Y., Choi K.C., Park S.H., et al. Extracellular signal-regulated protein kinase, but not c-Jun N-terminal kinase, is activated by type II gonadotropin-releasing hormone involved in the inhibition of ovarian cancer cell proliferation. J Clin Endocrinol Metab 2005, 90:1670-1677.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 1670-1677
    • Kim, K.Y.1    Choi, K.C.2    Park, S.H.3
  • 96
    • 33646014459 scopus 로고    scopus 로고
    • Mechanism of gonadotropin-releasing hormone (GnRH)-I and -II-induced cell growth inhibition in ovarian cancer cells: role of the GnRH-I receptor and protein kinase C pathway
    • Kim K.Y., Choi K.C., Auersperg N., et al. Mechanism of gonadotropin-releasing hormone (GnRH)-I and -II-induced cell growth inhibition in ovarian cancer cells: role of the GnRH-I receptor and protein kinase C pathway. Endocr Relat Cancer 2006, 13:211-220.
    • (2006) Endocr Relat Cancer , vol.13 , pp. 211-220
    • Kim, K.Y.1    Choi, K.C.2    Auersperg, N.3
  • 97
    • 0027465167 scopus 로고
    • Primary structure and biological activity of a third gonadotropin-releasing hormone from lamprey brain
    • Sower S.A., Chiang Y.C., Lovas S., et al. Primary structure and biological activity of a third gonadotropin-releasing hormone from lamprey brain. Endocrinology 1993, 132:1125-1131.
    • (1993) Endocrinology , vol.132 , pp. 1125-1131
    • Sower, S.A.1    Chiang, Y.C.2    Lovas, S.3
  • 98
    • 0028021169 scopus 로고
    • Effects of lamprey gonadotropin-releasing hormone-III on steroidogenesis and spermiation in male sea lampreys
    • Deragon K.L., Sower S.A. Effects of lamprey gonadotropin-releasing hormone-III on steroidogenesis and spermiation in male sea lampreys. Gen Comp Endocrinol 1994, 95:363-367.
    • (1994) Gen Comp Endocrinol , vol.95 , pp. 363-367
    • Deragon, K.L.1    Sower, S.A.2
  • 99
    • 0344141211 scopus 로고    scopus 로고
    • Direct anticancer activity of gonadotropin-releasing hormone-III
    • Lovas S., Palyi I., Vincze B., et al. Direct anticancer activity of gonadotropin-releasing hormone-III. J Pept Res 1998, 52:384-389.
    • (1998) J Pept Res , vol.52 , pp. 384-389
    • Lovas, S.1    Palyi, I.2    Vincze, B.3
  • 100
    • 0036668076 scopus 로고    scopus 로고
    • Lamprey gonadotropin hormone-releasing hormone-III has no selective follicle-stimulating hormone-releasing effect in rats
    • Kovacs M., Seprodi J., Koppan M., et al. Lamprey gonadotropin hormone-releasing hormone-III has no selective follicle-stimulating hormone-releasing effect in rats. J Neuroendocrinol 2002, 14:647-655.
    • (2002) J Neuroendocrinol , vol.14 , pp. 647-655
    • Kovacs, M.1    Seprodi, J.2    Koppan, M.3
  • 101
    • 33847405729 scopus 로고    scopus 로고
    • Structure-activity study on the LH- and FSH-releasing and anticancer effects of gonadotropin-releasing hormone (GnRH)-III analogs
    • Kovacs M., Vincze B., Horvath J.E., et al. Structure-activity study on the LH- and FSH-releasing and anticancer effects of gonadotropin-releasing hormone (GnRH)-III analogs. Peptides 2007, 28:821-829.
    • (2007) Peptides , vol.28 , pp. 821-829
    • Kovacs, M.1    Vincze, B.2    Horvath, J.E.3
  • 102
    • 0030937284 scopus 로고    scopus 로고
    • Molecular mechanisms of ligand interaction with the gonadotropin-releasing hormone receptor
    • Sealfon S.C., Weinstein H., Millar R.P. Molecular mechanisms of ligand interaction with the gonadotropin-releasing hormone receptor. Endocr Rev 1997, 18:180-205.
    • (1997) Endocr Rev , vol.18 , pp. 180-205
    • Sealfon, S.C.1    Weinstein, H.2    Millar, R.P.3
  • 103
    • 0023721848 scopus 로고
    • Endopeptidase-24.15 is the primary enzyme that degrades luteinizing hormone releasing hormone both in vitro and in vivo
    • Molineaux C.J., Lasdun A., Michaud C., et al. Endopeptidase-24.15 is the primary enzyme that degrades luteinizing hormone releasing hormone both in vitro and in vivo. J Neurochem 1988, 51:624-633.
    • (1988) J Neurochem , vol.51 , pp. 624-633
    • Molineaux, C.J.1    Lasdun, A.2    Michaud, C.3
  • 104
    • 0015905910 scopus 로고
    • The half-life, metabolism and excretion of tritiated luteinizing hormone-releasing hormone (LH-RH) in man
    • Redding T.W., Kastin A.J., Gonzales-Barcena D., et al. The half-life, metabolism and excretion of tritiated luteinizing hormone-releasing hormone (LH-RH) in man. J Clin Endocrinol Metab 1973, 37:626-631.
    • (1973) J Clin Endocrinol Metab , vol.37 , pp. 626-631
    • Redding, T.W.1    Kastin, A.J.2    Gonzales-Barcena, D.3
  • 106
    • 0022665939 scopus 로고
    • Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: rationale and perspective
    • Karten M.J., Rivier J.E. Gonadotropin-releasing hormone analog design. Structure-function studies toward the development of agonists and antagonists: rationale and perspective. Endocr Rev 1986, 7:44-66.
    • (1986) Endocr Rev , vol.7 , pp. 44-66
    • Karten, M.J.1    Rivier, J.E.2
  • 107
    • 24044474071 scopus 로고    scopus 로고
    • GnRH analogues - agonists and antagonists
    • Padula A.M. GnRH analogues - agonists and antagonists. Anim Reprod Sci 2005, 88:115-126.
    • (2005) Anim Reprod Sci , vol.88 , pp. 115-126
    • Padula, A.M.1
  • 108
    • 71449126523 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone antagonists
    • Mezo G., Manea M. Luteinizing hormone-releasing hormone antagonists. Expert Opin Ther Pat 2009, 19:1771-1785.
    • (2009) Expert Opin Ther Pat , vol.19 , pp. 1771-1785
    • Mezo, G.1    Manea, M.2
  • 109
    • 79960836271 scopus 로고    scopus 로고
    • Biochemistry, molecular biology and cell biology of gonadotropin-releasing hormone antagonists
    • Tan O., Bukulmez O. Biochemistry, molecular biology and cell biology of gonadotropin-releasing hormone antagonists. Curr Opin Obstet Gynecol 2011, 23:238-244.
    • (2011) Curr Opin Obstet Gynecol , vol.23 , pp. 238-244
    • Tan, O.1    Bukulmez, O.2
  • 110
    • 0035944837 scopus 로고    scopus 로고
    • Gonadotropin-releasing-hormone-receptor antagonists
    • Huirne J.A., Lambalk C.B. Gonadotropin-releasing-hormone-receptor antagonists. Lancet 2001, 358:1793-1803.
    • (2001) Lancet , vol.358 , pp. 1793-1803
    • Huirne, J.A.1    Lambalk, C.B.2
  • 111
    • 0033392782 scopus 로고    scopus 로고
    • LH-RH analogues: I. Their impact on reproductive medicine
    • Schally A.V. LH-RH analogues: I. Their impact on reproductive medicine. Gynecol Endocrinol 1999, 13:401-409.
    • (1999) Gynecol Endocrinol , vol.13 , pp. 401-409
    • Schally, A.V.1
  • 112
    • 0021246505 scopus 로고
    • [Ac-d-NAL(2)1,4Fd-Phe2, d-Trp3, d-Arg6]-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats
    • Schmidt F., Sundaram K., Thau R.B., et al. [Ac-d-NAL(2)1,4Fd-Phe2, d-Trp3, d-Arg6]-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats. Contraception 1984, 29:283-289.
    • (1984) Contraception , vol.29 , pp. 283-289
    • Schmidt, F.1    Sundaram, K.2    Thau, R.B.3
  • 113
    • 79955866326 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone receptor targeted agents for prostate cancer
    • Liu S.V., Liu S., Pinski J. Luteinizing hormone-releasing hormone receptor targeted agents for prostate cancer. Expert Opin Investig Drugs 2011, 20:769-778.
    • (2011) Expert Opin Investig Drugs , vol.20 , pp. 769-778
    • Liu, S.V.1    Liu, S.2    Pinski, J.3
  • 114
    • 77956374604 scopus 로고    scopus 로고
    • Ozarelix, a fourth generation GnRH antagonist, induces apoptosis in hormone refractory androgen receptor negative prostate cancer cells modulating expression and activity of death receptors
    • Festuccia C., Dondi D., Piccolella M., et al. Ozarelix, a fourth generation GnRH antagonist, induces apoptosis in hormone refractory androgen receptor negative prostate cancer cells modulating expression and activity of death receptors. Prostate 2010, 70:1340-1349.
    • (2010) Prostate , vol.70 , pp. 1340-1349
    • Festuccia, C.1    Dondi, D.2    Piccolella, M.3
  • 115
    • 24044499587 scopus 로고    scopus 로고
    • Leuprolide acetate given by a subcutaneous extended-release injection: less of a pain?
    • Cox M.C., Scripture C.D., Figg W.D. Leuprolide acetate given by a subcutaneous extended-release injection: less of a pain?. Expert Rev Anticancer Ther 2005, 5:605-611.
    • (2005) Expert Rev Anticancer Ther , vol.5 , pp. 605-611
    • Cox, M.C.1    Scripture, C.D.2    Figg, W.D.3
  • 116
    • 77349087142 scopus 로고    scopus 로고
    • Six-month depot formulation of leuprorelin acetate in the treatment of prostate cancer
    • Sethi R., Sanfilippo N. Six-month depot formulation of leuprorelin acetate in the treatment of prostate cancer. Clin Interv Aging 2009, 4:259-267.
    • (2009) Clin Interv Aging , vol.4 , pp. 259-267
    • Sethi, R.1    Sanfilippo, N.2
  • 117
    • 0021929895 scopus 로고
    • Studies of a controlled-release microcapsule formulation of an LH-RH agonist (D-Trp-6-LH-RH) in the rhesus monkey menstrual cycle
    • Asch R.H., Rojas F.J., Tice T.R., et al. Studies of a controlled-release microcapsule formulation of an LH-RH agonist (D-Trp-6-LH-RH) in the rhesus monkey menstrual cycle. Int J Fertil 1985, 30:19-26.
    • (1985) Int J Fertil , vol.30 , pp. 19-26
    • Asch, R.H.1    Rojas, F.J.2    Tice, T.R.3
  • 118
    • 0038139821 scopus 로고
    • Long-acting delivery systems for peptides: inhibition of rat prostate tumors by controlled release of [D-Trp6]luteinizing hormone-releasing hormone from injectable microcapsules
    • Redding T.W., Schally A.V., Tice T.R., et al. Long-acting delivery systems for peptides: inhibition of rat prostate tumors by controlled release of [D-Trp6]luteinizing hormone-releasing hormone from injectable microcapsules. Proc Natl Acad Sci USA 1984, 81:5845-5848.
    • (1984) Proc Natl Acad Sci USA , vol.81 , pp. 5845-5848
    • Redding, T.W.1    Schally, A.V.2    Tice, T.R.3
  • 119
    • 80955136887 scopus 로고    scopus 로고
    • Six-month gonadotropin releasing hormone (GnRH) agonist depots provide efficacy, safety, convenience, and comfort
    • Crawford E.D., Phillips J.M. Six-month gonadotropin releasing hormone (GnRH) agonist depots provide efficacy, safety, convenience, and comfort. Cancer Manag Res 2011, 3:201-209.
    • (2011) Cancer Manag Res , vol.3 , pp. 201-209
    • Crawford, E.D.1    Phillips, J.M.2
  • 120
    • 30344486309 scopus 로고    scopus 로고
    • A 12-month clinical study of LA-2585 (45.0 mg): a new 6-month subcutaneous delivery system for leuprolide acetate for the treatment of prostate cancer
    • Crawford E.D., Sartor O., Chu F., et al. A 12-month clinical study of LA-2585 (45.0 mg): a new 6-month subcutaneous delivery system for leuprolide acetate for the treatment of prostate cancer. J Urol 2006, 175:533-536.
    • (2006) J Urol , vol.175 , pp. 533-536
    • Crawford, E.D.1    Sartor, O.2    Chu, F.3
  • 121
    • 84857054586 scopus 로고    scopus 로고
    • Efficacy and safety of leuprolide acetate 6-month depot for suppression of testosterone in patients with prostate cancer
    • Spitz A., Young J.M., Larsen L., et al. Efficacy and safety of leuprolide acetate 6-month depot for suppression of testosterone in patients with prostate cancer. Prostate Cancer Prostatic Dis 2012, 15:93-99.
    • (2012) Prostate Cancer Prostatic Dis , vol.15 , pp. 93-99
    • Spitz, A.1    Young, J.M.2    Larsen, L.3
  • 122
    • 70449416221 scopus 로고    scopus 로고
    • Triptorelin 6-month formulation in the management of patients with locally advanced and metastatic prostate cancer: an open-label, non-comparative, multicentre, phase III study
    • Lundstrom E.A., Rencken R.K., van Wyk J.H., et al. Triptorelin 6-month formulation in the management of patients with locally advanced and metastatic prostate cancer: an open-label, non-comparative, multicentre, phase III study. Clin Drug Investig 2009, 29:757-765.
    • (2009) Clin Drug Investig , vol.29 , pp. 757-765
    • Lundstrom, E.A.1    Rencken, R.K.2    van Wyk, J.H.3
  • 123
    • 84655169252 scopus 로고    scopus 로고
    • Long-term efficacy and tolerability of once-yearly histrelin acetate subcutaneous implant in patients with advanced prostate cancer
    • Shore N., Cookson M.S., Gittelman M.C. Long-term efficacy and tolerability of once-yearly histrelin acetate subcutaneous implant in patients with advanced prostate cancer. BJU Int 2012, 109:226-232.
    • (2012) BJU Int , vol.109 , pp. 226-232
    • Shore, N.1    Cookson, M.S.2    Gittelman, M.C.3
  • 124
    • 78149444583 scopus 로고    scopus 로고
    • Triptorelin embonate: a 6-month formulation for prostate cancer
    • Whelan P. Triptorelin embonate: a 6-month formulation for prostate cancer. Expert Opin Pharmacother 2010, 11:2929-2932.
    • (2010) Expert Opin Pharmacother , vol.11 , pp. 2929-2932
    • Whelan, P.1
  • 125
    • 84862777685 scopus 로고    scopus 로고
    • Androgen-deprivation therapy for nonmetastatic prostate cancer is associated with an increased risk of peripheral arterial disease and venous thromboembolism
    • Hu J.C., Williams S.B., O'Malley A.J., et al. Androgen-deprivation therapy for nonmetastatic prostate cancer is associated with an increased risk of peripheral arterial disease and venous thromboembolism. Eur Urol 2012, 61:1119-1128.
    • (2012) Eur Urol , vol.61 , pp. 1119-1128
    • Hu, J.C.1    Williams, S.B.2    O'Malley, A.J.3
  • 126
    • 79951661266 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone agonists and the risks of type 2 diabetes and cardiovascular disease in men with prostate cancer
    • Saylor P.J., Keating N.L., Freedland S.J., et al. Gonadotropin-releasing hormone agonists and the risks of type 2 diabetes and cardiovascular disease in men with prostate cancer. Drugs 2011, 71:255-261.
    • (2011) Drugs , vol.71 , pp. 255-261
    • Saylor, P.J.1    Keating, N.L.2    Freedland, S.J.3
  • 127
    • 84858027124 scopus 로고    scopus 로고
    • Androgen deprivation and thromboembolic events in men with prostate cancer
    • Ehdaie B., Atoria C.L., Gupta A., et al. Androgen deprivation and thromboembolic events in men with prostate cancer. Cancer 2012, 118:3397-3406.
    • (2012) Cancer , vol.118 , pp. 3397-3406
    • Ehdaie, B.1    Atoria, C.L.2    Gupta, A.3
  • 128
    • 0034114889 scopus 로고    scopus 로고
    • Quality of life of asymptomatic men with nonmetastatic prostate cancer on androgen deprivation therapy
    • Herr H.W., O'Sullivan M. Quality of life of asymptomatic men with nonmetastatic prostate cancer on androgen deprivation therapy. J Urol 2000, 163:1743-1746.
    • (2000) J Urol , vol.163 , pp. 1743-1746
    • Herr, H.W.1    O'Sullivan, M.2
  • 129
    • 33646029746 scopus 로고    scopus 로고
    • Insulin sensitivity during combined androgen blockade for prostate cancer
    • Smith M.R., Lee H., Nathan D.M. Insulin sensitivity during combined androgen blockade for prostate cancer. J Clin Endocrinol Metab 2006, 91:1305-1308.
    • (2006) J Clin Endocrinol Metab , vol.91 , pp. 1305-1308
    • Smith, M.R.1    Lee, H.2    Nathan, D.M.3
  • 130
    • 0036096151 scopus 로고    scopus 로고
    • Changes in bone mineral density, lean body mass and fat content as measured by dual energy X-ray absorptiometry in patients with prostate cancer without apparent bone metastases given androgen deprivation therapy
    • discussion 2367
    • Berruti A., Dogliotti L., Terrone C., et al. Changes in bone mineral density, lean body mass and fat content as measured by dual energy X-ray absorptiometry in patients with prostate cancer without apparent bone metastases given androgen deprivation therapy. J Urol 2002, 167:2361-2367. discussion 2367.
    • (2002) J Urol , vol.167 , pp. 2361-2367
    • Berruti, A.1    Dogliotti, L.2    Terrone, C.3
  • 131
    • 11844252588 scopus 로고    scopus 로고
    • Risk of fracture after androgen deprivation for prostate cancer
    • Shahinian V.B., Kuo Y.F., Freeman J.L., et al. Risk of fracture after androgen deprivation for prostate cancer. N Engl J Med 2005, 352:154-164.
    • (2005) N Engl J Med , vol.352 , pp. 154-164
    • Shahinian, V.B.1    Kuo, Y.F.2    Freeman, J.L.3
  • 132
    • 22144484150 scopus 로고    scopus 로고
    • Androgen deprivation therapy for prostate cancer
    • Sharifi N., Gulley J.L., Dahut W.L. Androgen deprivation therapy for prostate cancer. JAMA 2005, 294:238-244.
    • (2005) JAMA , vol.294 , pp. 238-244
    • Sharifi, N.1    Gulley, J.L.2    Dahut, W.L.3
  • 133
    • 0025246690 scopus 로고
    • Effects of androgen withdrawal on the stem cell composition of the Shionogi carcinoma
    • Bruchovsky N., Rennie P.S., Coldman A.J., et al. Effects of androgen withdrawal on the stem cell composition of the Shionogi carcinoma. Cancer Res 1990, 50:2275-2282.
    • (1990) Cancer Res , vol.50 , pp. 2275-2282
    • Bruchovsky, N.1    Rennie, P.S.2    Coldman, A.J.3
  • 134
    • 84870571940 scopus 로고    scopus 로고
    • Intermittent hormonal therapy in the treatment of metastatic prostate cancer: a randomized trial
    • Mottet N., Van Damme J., Loulidi S., et al. Intermittent hormonal therapy in the treatment of metastatic prostate cancer: a randomized trial. BJU Int 2013, 63:121-122.
    • (2013) BJU Int , vol.63 , pp. 121-122
    • Mottet, N.1    Van Damme, J.2    Loulidi, S.3
  • 135
    • 58149144740 scopus 로고    scopus 로고
    • Will GnRH antagonists improve prostate cancer treatment?
    • Huhtaniemi I., White R., McArdle C.A., et al. Will GnRH antagonists improve prostate cancer treatment?. Trends Endocrinol Metab 2009, 20:43-50.
    • (2009) Trends Endocrinol Metab , vol.20 , pp. 43-50
    • Huhtaniemi, I.1    White, R.2    McArdle, C.A.3
  • 136
    • 84862767296 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone: an update review of the antagonists versus agonists
    • Van Poppel H., Klotz L. Gonadotropin-releasing hormone: an update review of the antagonists versus agonists. Int J Urol 2012, 19:594-601.
    • (2012) Int J Urol , vol.19 , pp. 594-601
    • Van Poppel, H.1    Klotz, L.2
  • 137
    • 80051764006 scopus 로고    scopus 로고
    • An update on the use of gonadotropin-releasing hormone antagonists in prostate cancer
    • Boccon-Gibod L., van der Meulen E., Persson B.E. An update on the use of gonadotropin-releasing hormone antagonists in prostate cancer. Ther Adv Urol 2011, 3:127-140.
    • (2011) Ther Adv Urol , vol.3 , pp. 127-140
    • Boccon-Gibod, L.1    van der Meulen, E.2    Persson, B.E.3
  • 138
    • 77956213440 scopus 로고    scopus 로고
    • GnRH antagonists in the treatment of advanced prostate cancer
    • Pommerville P.J., de Boer J.G. GnRH antagonists in the treatment of advanced prostate cancer. Can J Urol 2010, 17:5063-5070.
    • (2010) Can J Urol , vol.17 , pp. 5063-5070
    • Pommerville, P.J.1    de Boer, J.G.2
  • 139
    • 70449334504 scopus 로고    scopus 로고
    • Abarelix and other gonadotrophin-releasing hormone antagonists in prostate cancer
    • Kirby R.S., Fitzpatrick J.M., Clarke N. Abarelix and other gonadotrophin-releasing hormone antagonists in prostate cancer. BJU Int 2009, 104:1580-1584.
    • (2009) BJU Int , vol.104 , pp. 1580-1584
    • Kirby, R.S.1    Fitzpatrick, J.M.2    Clarke, N.3
  • 140
    • 0032739426 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone analogs: their impact on the control of tumorigenesis
    • Schally A.V. Luteinizing hormone-releasing hormone analogs: their impact on the control of tumorigenesis. Peptides 1999, 20:1247-1262.
    • (1999) Peptides , vol.20 , pp. 1247-1262
    • Schally, A.V.1
  • 142
    • 77957726553 scopus 로고    scopus 로고
    • Dose-ranging study of the luteinizing hormone-releasing hormone receptor antagonist cetrorelix pamoate in the treatment of patients with symptomatic benign prostatic hyperplasia
    • Debruyne F., Tzvetkov M., Altarac S., et al. Dose-ranging study of the luteinizing hormone-releasing hormone receptor antagonist cetrorelix pamoate in the treatment of patients with symptomatic benign prostatic hyperplasia. Urology 2010, 76:927-933.
    • (2010) Urology , vol.76 , pp. 927-933
    • Debruyne, F.1    Tzvetkov, M.2    Altarac, S.3
  • 143
    • 0035046991 scopus 로고    scopus 로고
    • The gonadotropin-releasing hormone antagonist abarelix depot versus luteinizing hormone releasing hormone agonists leuprolide or goserelin: initial results of endocrinological and biochemical efficacies in patients with prostate cancer
    • Tomera K., Gleason D., Gittelman M., et al. The gonadotropin-releasing hormone antagonist abarelix depot versus luteinizing hormone releasing hormone agonists leuprolide or goserelin: initial results of endocrinological and biochemical efficacies in patients with prostate cancer. J Urol 2001, 165:1585-1589.
    • (2001) J Urol , vol.165 , pp. 1585-1589
    • Tomera, K.1    Gleason, D.2    Gittelman, M.3
  • 144
    • 0035516095 scopus 로고    scopus 로고
    • A phase 3, multicenter, open-label, randomized study of abarelix versus leuprolide acetate in men with prostate cancer
    • McLeod D., Zinner N., Tomera K., et al. A phase 3, multicenter, open-label, randomized study of abarelix versus leuprolide acetate in men with prostate cancer. Urology 2001, 58:756-761.
    • (2001) Urology , vol.58 , pp. 756-761
    • McLeod, D.1    Zinner, N.2    Tomera, K.3
  • 145
    • 0242664216 scopus 로고    scopus 로고
    • An open-label study of abarelix in men with symptomatic prostate cancer at risk of treatment with LHRH agonists
    • Koch M., Steidle C., Brosman S., et al. An open-label study of abarelix in men with symptomatic prostate cancer at risk of treatment with LHRH agonists. Urology 2003, 62:877-882.
    • (2003) Urology , vol.62 , pp. 877-882
    • Koch, M.1    Steidle, C.2    Brosman, S.3
  • 146
    • 0036128522 scopus 로고    scopus 로고
    • A phase 3, multicenter, open label, randomized study of abarelix versus leuprolide plus daily antiandrogen in men with prostate cancer
    • Trachtenberg J., Gittleman M., Steidle C., et al. A phase 3, multicenter, open label, randomized study of abarelix versus leuprolide plus daily antiandrogen in men with prostate cancer. J Urol 2002, 167:1670-1674.
    • (2002) J Urol , vol.167 , pp. 1670-1674
    • Trachtenberg, J.1    Gittleman, M.2    Steidle, C.3
  • 147
    • 1942476114 scopus 로고    scopus 로고
    • Pharmacokinetics and pharmacodynamics of a novel depot formulation of abarelix, a gonadotropin-releasing hormone (GnRH) antagonist, in healthy men ages 50 to 75
    • Wong S.L., Lau D.T., Baughman S.A., et al. Pharmacokinetics and pharmacodynamics of a novel depot formulation of abarelix, a gonadotropin-releasing hormone (GnRH) antagonist, in healthy men ages 50 to 75. J Clin Pharmacol 2004, 44:495-502.
    • (2004) J Clin Pharmacol , vol.44 , pp. 495-502
    • Wong, S.L.1    Lau, D.T.2    Baughman, S.A.3
  • 148
    • 84857576096 scopus 로고    scopus 로고
    • New treatment paradigm for prostate cancer: abarelix initiation therapy for immediate testosterone suppression followed by a luteinizing hormone-releasing hormone agonist
    • Garnick M.B., Mottet N. New treatment paradigm for prostate cancer: abarelix initiation therapy for immediate testosterone suppression followed by a luteinizing hormone-releasing hormone agonist. BJU Int 2012, 110:499-504.
    • (2012) BJU Int , vol.110 , pp. 499-504
    • Garnick, M.B.1    Mottet, N.2
  • 149
    • 6444243321 scopus 로고    scopus 로고
    • Abarelix: the first gonadotrophin-releasing hormone antagonist for the treatment of prostate cancer
    • Mongiat-Artus P., Teillac P. Abarelix: the first gonadotrophin-releasing hormone antagonist for the treatment of prostate cancer. Expert Opin Pharmacother 2004, 5:2171-2179.
    • (2004) Expert Opin Pharmacother , vol.5 , pp. 2171-2179
    • Mongiat-Artus, P.1    Teillac, P.2
  • 150
    • 80755177060 scopus 로고    scopus 로고
    • New data, new paradigms for treating prostate cancer patients - VI: novel hormonal therapy approaches
    • Dreicer R., Bajorin D.F., McLeod D.G., et al. New data, new paradigms for treating prostate cancer patients - VI: novel hormonal therapy approaches. Urology 2011, 78:S494-498.
    • (2011) Urology , vol.78
    • Dreicer, R.1    Bajorin, D.F.2    McLeod, D.G.3
  • 151
    • 74749105209 scopus 로고    scopus 로고
    • Degarelix: a gonadotropin-releasing hormone antagonist for the management of prostate cancer
    • Steinberg M. Degarelix: a gonadotropin-releasing hormone antagonist for the management of prostate cancer. Clin Ther 2009, 31(Pt 2):2312-2331.
    • (2009) Clin Ther , vol.31 , Issue.PART 2 , pp. 2312-2331
    • Steinberg, M.1
  • 152
    • 84873704195 scopus 로고    scopus 로고
    • New considerations for ADT in advanced prostate cancer and the emerging role of GnRH antagonists
    • Shore N.D., Abrahamsson P.A., Anderson J., et al. New considerations for ADT in advanced prostate cancer and the emerging role of GnRH antagonists. Prostate Cancer Prostatic Dis 2012, 10.1038/pcan.2012.25.
    • (2012) Prostate Cancer Prostatic Dis
    • Shore, N.D.1    Abrahamsson, P.A.2    Anderson, J.3
  • 153
    • 84862983937 scopus 로고    scopus 로고
    • The effect of baseline testosterone on the efficacy of degarelix and leuprolide: further insights from a 12-month, comparative, phase III study in prostate cancer patients
    • Damber J.E., Tammela T.L., Iversen P., et al. The effect of baseline testosterone on the efficacy of degarelix and leuprolide: further insights from a 12-month, comparative, phase III study in prostate cancer patients. Urology 2012, 80:174-181.
    • (2012) Urology , vol.80 , pp. 174-181
    • Damber, J.E.1    Tammela, T.L.2    Iversen, P.3
  • 154
    • 80051550573 scopus 로고    scopus 로고
    • A phase III extension trial with a 1-arm crossover from leuprolide to degarelix: comparison of gonadotropin-releasing hormone agonist and antagonist effect on prostate cancer
    • Crawford E.D., Tombal B., Miller K., et al. A phase III extension trial with a 1-arm crossover from leuprolide to degarelix: comparison of gonadotropin-releasing hormone agonist and antagonist effect on prostate cancer. J Urol 2011, 186:889-897.
    • (2011) J Urol , vol.186 , pp. 889-897
    • Crawford, E.D.1    Tombal, B.2    Miller, K.3
  • 155
    • 0035253568 scopus 로고    scopus 로고
    • GnRH antagonists: a new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6
    • Jiang G., Stalewski J., Galyean R., et al. GnRH antagonists: a new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6. J Med Chem 2001, 44:453-467.
    • (2001) J Med Chem , vol.44 , pp. 453-467
    • Jiang, G.1    Stalewski, J.2    Galyean, R.3
  • 156
    • 33847129303 scopus 로고    scopus 로고
    • Rapid suppression of plasma testosterone levels and tumor growth in the dunning rat model treated with degarelix, a new gonadotropin-releasing hormone antagonist
    • Princivalle M., Broqua P., White R., et al. Rapid suppression of plasma testosterone levels and tumor growth in the dunning rat model treated with degarelix, a new gonadotropin-releasing hormone antagonist. J Pharmacol Exp Ther 2007, 320:1113-1118.
    • (2007) J Pharmacol Exp Ther , vol.320 , pp. 1113-1118
    • Princivalle, M.1    Broqua, P.2    White, R.3
  • 157
    • 0036129344 scopus 로고    scopus 로고
    • Pharmacological profile of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix
    • Broqua P., Riviere P.J., Conn P.M., et al. Pharmacological profile of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix. J Pharmacol Exp Ther 2002, 301:95-102.
    • (2002) J Pharmacol Exp Ther , vol.301 , pp. 95-102
    • Broqua, P.1    Riviere, P.J.2    Conn, P.M.3
  • 158
    • 77956605441 scopus 로고    scopus 로고
    • Degarelix, a novel GnRH antagonist, causes minimal histamine release compared with cetrorelix, abarelix and ganirelix in an ex vivo model of human skin samples
    • Koechling W., Hjortkjaer R., Tanko L.B. Degarelix, a novel GnRH antagonist, causes minimal histamine release compared with cetrorelix, abarelix and ganirelix in an ex vivo model of human skin samples. Br J Clin Pharmacol 2010, 70:580-587.
    • (2010) Br J Clin Pharmacol , vol.70 , pp. 580-587
    • Koechling, W.1    Hjortkjaer, R.2    Tanko, L.B.3
  • 159
    • 53249121469 scopus 로고    scopus 로고
    • A 1-year, open label, randomized phase II dose finding study of degarelix for the treatment of prostate cancer in North America
    • Gittelman M., Pommerville P.J., Persson B.E., et al. A 1-year, open label, randomized phase II dose finding study of degarelix for the treatment of prostate cancer in North America. J Urol 2008, 180:1986-1992.
    • (2008) J Urol , vol.180 , pp. 1986-1992
    • Gittelman, M.1    Pommerville, P.J.2    Persson, B.E.3
  • 160
    • 50849110501 scopus 로고    scopus 로고
    • Degarelix: a novel gonadotropin-releasing hormone (GnRH) receptor blocker - results from a 1-yr, multicentre, randomised, phase 2 dosage-finding study in the treatment of prostate cancer
    • Van Poppel H., Tombal B., de la Rosette J.J., et al. Degarelix: a novel gonadotropin-releasing hormone (GnRH) receptor blocker - results from a 1-yr, multicentre, randomised, phase 2 dosage-finding study in the treatment of prostate cancer. Eur Urol 2008, 54:805-813.
    • (2008) Eur Urol , vol.54 , pp. 805-813
    • Van Poppel, H.1    Tombal, B.2    de la Rosette, J.J.3
  • 161
    • 56649116179 scopus 로고    scopus 로고
    • The efficacy and safety of degarelix: a 12-month, comparative, randomized, open-label, parallel-group phase III study in patients with prostate cancer
    • Klotz L., Boccon-Gibod L., Shore N.D., et al. The efficacy and safety of degarelix: a 12-month, comparative, randomized, open-label, parallel-group phase III study in patients with prostate cancer. BJU Int 2008, 102:1531-1538.
    • (2008) BJU Int , vol.102 , pp. 1531-1538
    • Klotz, L.1    Boccon-Gibod, L.2    Shore, N.D.3
  • 162
    • 84872904175 scopus 로고    scopus 로고
    • Rapid elimination kinetics of free PSA or human kallikrein-related peptidase 2 after initiation of gonadotropin-releasing hormone-antagonist treatment of prostate cancer: potential for rapid monitoring of treatment responses
    • Ulmert D., Vickers A.J., Scher H.I., et al. Rapid elimination kinetics of free PSA or human kallikrein-related peptidase 2 after initiation of gonadotropin-releasing hormone-antagonist treatment of prostate cancer: potential for rapid monitoring of treatment responses. Clin Chem Lab Med 2012, 1-6.
    • (2012) Clin Chem Lab Med , pp. 1-6
    • Ulmert, D.1    Vickers, A.J.2    Scher, H.I.3
  • 163
    • 84870946305 scopus 로고    scopus 로고
    • Androgen deprivation therapy for volume reduction, lower urinary tract symptom relief and quality of life improvement in patients with prostate cancer: degarelix vs goserelin plus bicalutamide
    • Axcrona K., Aaltomaa S., da Silva C.M., et al. Androgen deprivation therapy for volume reduction, lower urinary tract symptom relief and quality of life improvement in patients with prostate cancer: degarelix vs goserelin plus bicalutamide. BJU Int 2012, 110:1721-1728.
    • (2012) BJU Int , vol.110 , pp. 1721-1728
    • Axcrona, K.1    Aaltomaa, S.2    da Silva, C.M.3
  • 164
    • 80053932202 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone blockers and cardiovascular disease risk: analysis of prospective clinical trials of degarelix
    • Smith M.R., Klotz L., van der Meulen E., et al. Gonadotropin-releasing hormone blockers and cardiovascular disease risk: analysis of prospective clinical trials of degarelix. J Urol 2011, 186:1835-1842.
    • (2011) J Urol , vol.186 , pp. 1835-1842
    • Smith, M.R.1    Klotz, L.2    van der Meulen, E.3
  • 165
    • 79956132880 scopus 로고    scopus 로고
    • Hot flushes in prostatic cancer patients during androgen-deprivation therapy with monthly dose of degarelix or leuprolide
    • Iversen P., Karup C., van der Meulen E., et al. Hot flushes in prostatic cancer patients during androgen-deprivation therapy with monthly dose of degarelix or leuprolide. Prostate Cancer Prostatic Dis 2011, 14:184-190.
    • (2011) Prostate Cancer Prostatic Dis , vol.14 , pp. 184-190
    • Iversen, P.1    Karup, C.2    van der Meulen, E.3
  • 166
    • 79955012057 scopus 로고    scopus 로고
    • Efficacy and safety of androgen deprivation therapy after switching from monthly leuprolide to monthly degarelix in patients with prostate cancer
    • de la Rosette J., Davis R., Frankel D., et al. Efficacy and safety of androgen deprivation therapy after switching from monthly leuprolide to monthly degarelix in patients with prostate cancer. Int J Clin Pract 2011, 65:559-566.
    • (2011) Int J Clin Pract , vol.65 , pp. 559-566
    • de la Rosette, J.1    Davis, R.2    Frankel, D.3
  • 167
    • 44849105587 scopus 로고    scopus 로고
    • 2-Phenyl-4-piperazinylbenzimidazoles: orally active inhibitors of the gonadotropin releasing hormone (GnRH) receptor
    • Pelletier J.C., Chengalvala M., Cottom J., et al. 2-Phenyl-4-piperazinylbenzimidazoles: orally active inhibitors of the gonadotropin releasing hormone (GnRH) receptor. Bioorg Med Chem 2008, 16:6617-6640.
    • (2008) Bioorg Med Chem , vol.16 , pp. 6617-6640
    • Pelletier, J.C.1    Chengalvala, M.2    Cottom, J.3
  • 168
    • 45749121193 scopus 로고    scopus 로고
    • Non-peptide gonadotropin-releasing hormone receptor antagonists
    • Betz S.F., Zhu Y.F., Chen C., et al. Non-peptide gonadotropin-releasing hormone receptor antagonists. J Med Chem 2008, 51:3331-3348.
    • (2008) J Med Chem , vol.51 , pp. 3331-3348
    • Betz, S.F.1    Zhu, Y.F.2    Chen, C.3
  • 169
    • 0037405120 scopus 로고    scopus 로고
    • Biological characterization of a novel, orally active small molecule gonadotropin-releasing hormone (GnRH) antagonist using castrated and intact rats
    • Anderes K.L., Luthin D.R., Castillo R., et al. Biological characterization of a novel, orally active small molecule gonadotropin-releasing hormone (GnRH) antagonist using castrated and intact rats. J Pharmacol Exp Ther 2003, 305:688-695.
    • (2003) J Pharmacol Exp Ther , vol.305 , pp. 688-695
    • Anderes, K.L.1    Luthin, D.R.2    Castillo, R.3
  • 170
    • 80054969959 scopus 로고    scopus 로고
    • Silicon analogues of the nonpeptidic GnRH antagonist AG-045572: syntheses, crystal structure analyses, and pharmacological characterization
    • Barnes M.J., Burschka C., Buttner M.W., et al. Silicon analogues of the nonpeptidic GnRH antagonist AG-045572: syntheses, crystal structure analyses, and pharmacological characterization. ChemMedChem 2011, 6:2070-2080.
    • (2011) ChemMedChem , vol.6 , pp. 2070-2080
    • Barnes, M.J.1    Burschka, C.2    Buttner, M.W.3
  • 171
    • 0036182849 scopus 로고    scopus 로고
    • Expression of receptors for luteinizing hormone-releasing hormone in human ovarian and endometrial cancers: frequency, autoregulation, and correlation with direct antiproliferative activity of luteinizing hormone-releasing hormone analogues
    • Volker P., Grundker C., Schmidt O., et al. Expression of receptors for luteinizing hormone-releasing hormone in human ovarian and endometrial cancers: frequency, autoregulation, and correlation with direct antiproliferative activity of luteinizing hormone-releasing hormone analogues. Am J Obstet Gynecol 2002, 186:171-179.
    • (2002) Am J Obstet Gynecol , vol.186 , pp. 171-179
    • Volker, P.1    Grundker, C.2    Schmidt, O.3
  • 172
    • 0027944974 scopus 로고
    • Presence of gonadotropin-releasing hormone receptor and its messenger ribonucleic acid in endometrial carcinoma and endometrium
    • Imai A., Ohno T., Iida K., et al. Presence of gonadotropin-releasing hormone receptor and its messenger ribonucleic acid in endometrial carcinoma and endometrium. Gynecol Oncol 1994, 55:144-148.
    • (1994) Gynecol Oncol , vol.55 , pp. 144-148
    • Imai, A.1    Ohno, T.2    Iida, K.3
  • 173
    • 0027532290 scopus 로고
    • Characterization of binding sites for a GnRH-agonist (buserelin) in human breast cancer biopsies and their distribution in relation to tumor parameters
    • Baumann K.H., Kiesel L., Kaufmann M., et al. Characterization of binding sites for a GnRH-agonist (buserelin) in human breast cancer biopsies and their distribution in relation to tumor parameters. Breast Cancer Res Treat 1993, 25:37-46.
    • (1993) Breast Cancer Res Treat , vol.25 , pp. 37-46
    • Baumann, K.H.1    Kiesel, L.2    Kaufmann, M.3
  • 174
    • 0027411778 scopus 로고
    • Expression of luteinizing hormone-releasing hormone mRNA in the human prostatic cancer cell line LNCaP
    • Limonta P., Dondi D., Moretti R.M., et al. Expression of luteinizing hormone-releasing hormone mRNA in the human prostatic cancer cell line LNCaP. J Clin Endocrinol Metab 1993, 76:797-800.
    • (1993) J Clin Endocrinol Metab , vol.76 , pp. 797-800
    • Limonta, P.1    Dondi, D.2    Moretti, R.M.3
  • 175
    • 0027941068 scopus 로고
    • Antiproliferative effects of luteinizing hormone-releasing hormone (LHRH) agonists on human androgen-independent prostate cancer cell line DU 145: evidence for an autocrine-inhibitory LHRH loop
    • Dondi D., Limonta P., Moretti R.M., et al. Antiproliferative effects of luteinizing hormone-releasing hormone (LHRH) agonists on human androgen-independent prostate cancer cell line DU 145: evidence for an autocrine-inhibitory LHRH loop. Cancer Res 1994, 54:4091-4095.
    • (1994) Cancer Res , vol.54 , pp. 4091-4095
    • Dondi, D.1    Limonta, P.2    Moretti, R.M.3
  • 176
    • 0025647639 scopus 로고
    • Receptors for luteinizing hormone-releasing hormone (LHRH) in Dunning R3327 prostate cancers and rat anterior pituitaries after treatment with a sustained delivery system of LHRH antagonist SB-75
    • Srkalovic G., Bokser L., Radulovic S., et al. Receptors for luteinizing hormone-releasing hormone (LHRH) in Dunning R3327 prostate cancers and rat anterior pituitaries after treatment with a sustained delivery system of LHRH antagonist SB-75. Endocrinology 1990, 127:3052-3060.
    • (1990) Endocrinology , vol.127 , pp. 3052-3060
    • Srkalovic, G.1    Bokser, L.2    Radulovic, S.3
  • 177
    • 0033303530 scopus 로고    scopus 로고
    • The luteinizing hormone-releasing hormone receptor in human prostate cancer cells: messenger ribonucleic acid expression, molecular size, and signal transduction pathway
    • Limonta P., Moretti R.M., Marelli M.M., et al. The luteinizing hormone-releasing hormone receptor in human prostate cancer cells: messenger ribonucleic acid expression, molecular size, and signal transduction pathway. Endocrinology 1999, 140:5250-5256.
    • (1999) Endocrinology , vol.140 , pp. 5250-5256
    • Limonta, P.1    Moretti, R.M.2    Marelli, M.M.3
  • 178
    • 0033963203 scopus 로고    scopus 로고
    • High incidence of receptors for luteinizing hormone-releasing hormone (LHRH) and LHRH receptor gene expression in human prostate cancers
    • Halmos G., Arencibia J.M., Schally A.V., et al. High incidence of receptors for luteinizing hormone-releasing hormone (LHRH) and LHRH receptor gene expression in human prostate cancers. J Urol 2000, 163:623-629.
    • (2000) J Urol , vol.163 , pp. 623-629
    • Halmos, G.1    Arencibia, J.M.2    Schally, A.V.3
  • 179
    • 0034892041 scopus 로고    scopus 로고
    • Increased incidence of luteinizing hormone-releasing hormone receptor gene messenger RNA expression in hormone-refractory human prostate cancers
    • Straub B., Muller M., Krause H., et al. Increased incidence of luteinizing hormone-releasing hormone receptor gene messenger RNA expression in hormone-refractory human prostate cancers. Clin Cancer Res 2001, 7:2340-2343.
    • (2001) Clin Cancer Res , vol.7 , pp. 2340-2343
    • Straub, B.1    Muller, M.2    Krause, H.3
  • 180
    • 0038353479 scopus 로고    scopus 로고
    • Real-time quantitative reverse transcriptase-polymerase chain reaction for luteinizing hormone-releasing hormone receptor gene mRNA expression in human prostate cancer
    • Straub B., Muller M., Krause H., et al. Real-time quantitative reverse transcriptase-polymerase chain reaction for luteinizing hormone-releasing hormone receptor gene mRNA expression in human prostate cancer. Urology 2003, 62:172-176.
    • (2003) Urology , vol.62 , pp. 172-176
    • Straub, B.1    Muller, M.2    Krause, H.3
  • 181
    • 27844465409 scopus 로고    scopus 로고
    • Immunohistochemical demonstration of gonadotropin-releasing hormone receptors in prostate carcinoma
    • Szabo J., Vegh A., Racz G., et al. Immunohistochemical demonstration of gonadotropin-releasing hormone receptors in prostate carcinoma. Urol Oncol 2005, 23:399-401.
    • (2005) Urol Oncol , vol.23 , pp. 399-401
    • Szabo, J.1    Vegh, A.2    Racz, G.3
  • 182
    • 19944405794 scopus 로고    scopus 로고
    • Evidence that prostate gonadotropin-releasing hormone receptors mediate an anti-tumourigenic response to analogue therapy in hormone refractory prostate cancer
    • Gnanapragasam V.J., Darby S., Khan M.M., et al. Evidence that prostate gonadotropin-releasing hormone receptors mediate an anti-tumourigenic response to analogue therapy in hormone refractory prostate cancer. J Pathol 2005, 206:205-213.
    • (2005) J Pathol , vol.206 , pp. 205-213
    • Gnanapragasam, V.J.1    Darby, S.2    Khan, M.M.3
  • 183
    • 0035371234 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptor expression in the human prostate
    • Tieva A., Stattin P., Wikstrom P., et al. Gonadotropin-releasing hormone receptor expression in the human prostate. Prostate 2001, 47:276-284.
    • (2001) Prostate , vol.47 , pp. 276-284
    • Tieva, A.1    Stattin, P.2    Wikstrom, P.3
  • 184
    • 0036667892 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptors in prostate tissue
    • Bono A.V., Salvadore M., Celato N. Gonadotropin-releasing hormone receptors in prostate tissue. Anal Quant Cytol Histol 2002, 24:221-227.
    • (2002) Anal Quant Cytol Histol , vol.24 , pp. 221-227
    • Bono, A.V.1    Salvadore, M.2    Celato, N.3
  • 185
    • 0037937558 scopus 로고    scopus 로고
    • Inhibitory activity of luteinizing hormone-releasing hormone on tumor growth and progression
    • Moretti R.M., Monagnani Marelli M., van Groeninghen J.C., et al. Inhibitory activity of luteinizing hormone-releasing hormone on tumor growth and progression. Endocr Relat Cancer 2003, 10:161-167.
    • (2003) Endocr Relat Cancer , vol.10 , pp. 161-167
    • Moretti, R.M.1    Monagnani Marelli, M.2    van Groeninghen, J.C.3
  • 186
    • 77957274069 scopus 로고    scopus 로고
    • Dual targeting of tumor and endothelial cells by gonadotropin-releasing hormone agonists to reduce melanoma angiogenesis
    • Moretti R.M., Mai S., Montagnani Marelli M., et al. Dual targeting of tumor and endothelial cells by gonadotropin-releasing hormone agonists to reduce melanoma angiogenesis. Endocrinology 2010, 151:4643-4653.
    • (2010) Endocrinology , vol.151 , pp. 4643-4653
    • Moretti, R.M.1    Mai, S.2    Montagnani Marelli, M.3
  • 187
    • 0030155790 scopus 로고    scopus 로고
    • Signal transduction of GnRH receptor in the reproductive tract tumor
    • Imai A., Horibe S., Takagi H., et al. Signal transduction of GnRH receptor in the reproductive tract tumor. Endocr J 1996, 43:249-260.
    • (1996) Endocr J , vol.43 , pp. 249-260
    • Imai, A.1    Horibe, S.2    Takagi, H.3
  • 188
    • 0030067871 scopus 로고    scopus 로고
    • Evidence for coupling of phosphotyrosine phosphatase to gonadotropin-releasing hormone receptor in ovarian carcinoma membrane
    • Imai A., Takagi H., Furui T., et al. Evidence for coupling of phosphotyrosine phosphatase to gonadotropin-releasing hormone receptor in ovarian carcinoma membrane. Cancer 1996, 77:132-137.
    • (1996) Cancer , vol.77 , pp. 132-137
    • Imai, A.1    Takagi, H.2    Furui, T.3
  • 189
    • 5644247440 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone (GnRH) antagonists promote proapoptotic signaling in peripheral reproductive tumor cells by activating a Galphai-coupling state of the type I GnRH receptor
    • Maudsley S., Davidson L., Pawson A.J., et al. Gonadotropin-releasing hormone (GnRH) antagonists promote proapoptotic signaling in peripheral reproductive tumor cells by activating a Galphai-coupling state of the type I GnRH receptor. Cancer Res 2004, 64:7533-7544.
    • (2004) Cancer Res , vol.64 , pp. 7533-7544
    • Maudsley, S.1    Davidson, L.2    Pawson, A.J.3
  • 190
    • 79955581160 scopus 로고    scopus 로고
    • Elevated GnRH receptor expression plus GnRH agonist treatment inhibits the growth of a subset of papillomavirus 18-immortalized human prostate cells
    • Morgan K., Stavrou E., Leighton S.P., et al. Elevated GnRH receptor expression plus GnRH agonist treatment inhibits the growth of a subset of papillomavirus 18-immortalized human prostate cells. Prostate 2011, 71:915-928.
    • (2011) Prostate , vol.71 , pp. 915-928
    • Morgan, K.1    Stavrou, E.2    Leighton, S.P.3
  • 191
    • 33644992893 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone in apoptosis of prostate cancer cells
    • Kraus S., Naor Z., Seger R. Gonadotropin-releasing hormone in apoptosis of prostate cancer cells. Cancer Lett 2006, 234:109-123.
    • (2006) Cancer Lett , vol.234 , pp. 109-123
    • Kraus, S.1    Naor, Z.2    Seger, R.3
  • 192
    • 4143145476 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone induces apoptosis of prostate cancer cells: role of c-Jun NH2-terminal kinase, protein kinase B, and extracellular signal-regulated kinase pathways
    • Kraus S., Levy G., Hanoch T., et al. Gonadotropin-releasing hormone induces apoptosis of prostate cancer cells: role of c-Jun NH2-terminal kinase, protein kinase B, and extracellular signal-regulated kinase pathways. Cancer Res 2004, 64:5736-5744.
    • (2004) Cancer Res , vol.64 , pp. 5736-5744
    • Kraus, S.1    Levy, G.2    Hanoch, T.3
  • 193
    • 0035848705 scopus 로고    scopus 로고
    • Reverse phase protein microarrays which capture disease progression show activation of pro-survival pathways at the cancer invasion front
    • Paweletz C.P., Charboneau L., Bichsel V.E., et al. Reverse phase protein microarrays which capture disease progression show activation of pro-survival pathways at the cancer invasion front. Oncogene 2001, 20:1981-1989.
    • (2001) Oncogene , vol.20 , pp. 1981-1989
    • Paweletz, C.P.1    Charboneau, L.2    Bichsel, V.E.3
  • 194
    • 0036554734 scopus 로고    scopus 로고
    • Immunohistochemical demonstration of phospho-Akt in high Gleason grade prostate cancer
    • Malik S.N., Brattain M., Ghosh P.M., et al. Immunohistochemical demonstration of phospho-Akt in high Gleason grade prostate cancer. Clin Cancer Res 2002, 8:1168-1171.
    • (2002) Clin Cancer Res , vol.8 , pp. 1168-1171
    • Malik, S.N.1    Brattain, M.2    Ghosh, P.M.3
  • 195
    • 0034637524 scopus 로고    scopus 로고
    • Increased AKT activity contributes to prostate cancer progression by dramatically accelerating prostate tumor growth and diminishing p27Kip1 expression
    • Graff J.R., Konicek B.W., McNulty A.M., et al. Increased AKT activity contributes to prostate cancer progression by dramatically accelerating prostate tumor growth and diminishing p27Kip1 expression. J Biol Chem 2000, 275:24500-24505.
    • (2000) J Biol Chem , vol.275 , pp. 24500-24505
    • Graff, J.R.1    Konicek, B.W.2    McNulty, A.M.3
  • 196
    • 39049181907 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone agonists reduce the migratory and the invasive behavior of androgen-independent prostate cancer cells by interfering with the activity of IGF-I
    • Montagnani Marelli M., Moretti R.M., Mai S., et al. Gonadotropin-releasing hormone agonists reduce the migratory and the invasive behavior of androgen-independent prostate cancer cells by interfering with the activity of IGF-I. Int J Oncol 2007, 30:261-271.
    • (2007) Int J Oncol , vol.30 , pp. 261-271
    • Montagnani Marelli, M.1    Moretti, R.M.2    Mai, S.3
  • 197
    • 14844288903 scopus 로고    scopus 로고
    • Luteinising hormone-releasing hormone analogue reverses the cell adhesion profile of EGFR overexpressing DU-145 human prostate carcinoma subline
    • Yates C., Wells A., Turner T. Luteinising hormone-releasing hormone analogue reverses the cell adhesion profile of EGFR overexpressing DU-145 human prostate carcinoma subline. Br J Cancer 2005, 92:366-375.
    • (2005) Br J Cancer , vol.92 , pp. 366-375
    • Yates, C.1    Wells, A.2    Turner, T.3
  • 198
    • 10344248844 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone agonists interfere with the stimulatory actions of epidermal growth factor in human prostatic cancer cell lines, LNCaP and DU 145
    • Moretti R.M., Marelli M.M., Dondi D., et al. Luteinizing hormone-releasing hormone agonists interfere with the stimulatory actions of epidermal growth factor in human prostatic cancer cell lines, LNCaP and DU 145. J Clin Endocrinol Metab 1996, 81:3930-3937.
    • (1996) J Clin Endocrinol Metab , vol.81 , pp. 3930-3937
    • Moretti, R.M.1    Marelli, M.M.2    Dondi, D.3
  • 199
    • 0032922082 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone agonists interfere with the mitogenic activity of the insulin-like growth factor system in androgen-independent prostate cancer cells
    • Marelli M.M., Moretti R.M., Dondi D., et al. Luteinizing hormone-releasing hormone agonists interfere with the mitogenic activity of the insulin-like growth factor system in androgen-independent prostate cancer cells. Endocrinology 1999, 140:329-334.
    • (1999) Endocrinology , vol.140 , pp. 329-334
    • Marelli, M.M.1    Moretti, R.M.2    Dondi, D.3
  • 200
    • 0033630476 scopus 로고    scopus 로고
    • GnRH receptor and apoptotic signaling
    • Imai A., Tamaya T. GnRH receptor and apoptotic signaling. Vitam Horm 2000, 59:1-33.
    • (2000) Vitam Horm , vol.59 , pp. 1-33
    • Imai, A.1    Tamaya, T.2
  • 201
    • 54849408590 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone: GnRH receptor signaling in extrapituitary tissues
    • Cheung L.W., Wong A.S. Gonadotropin-releasing hormone: GnRH receptor signaling in extrapituitary tissues. FEBS J 2008, 275:5479-5495.
    • (2008) FEBS J , vol.275 , pp. 5479-5495
    • Cheung, L.W.1    Wong, A.S.2
  • 202
    • 0026716297 scopus 로고
    • Antiproliferative effects of luteinizing hormone-releasing hormone agonists on the human prostatic cancer cell line LNCaP
    • Limonta P., Dondi D., Moretti R.M., et al. Antiproliferative effects of luteinizing hormone-releasing hormone agonists on the human prostatic cancer cell line LNCaP. J Clin Endocrinol Metab 1992, 75:207-212.
    • (1992) J Clin Endocrinol Metab , vol.75 , pp. 207-212
    • Limonta, P.1    Dondi, D.2    Moretti, R.M.3
  • 203
    • 0031960297 scopus 로고    scopus 로고
    • Growth-inhibitory effects of luteinizing hormone-releasing hormone (LHRH) agonists on xenografts of the DU 145 human androgen-independent prostate cancer cell line in nude mice
    • Dondi D., Moretti R.M., Montagnani Marelli M., et al. Growth-inhibitory effects of luteinizing hormone-releasing hormone (LHRH) agonists on xenografts of the DU 145 human androgen-independent prostate cancer cell line in nude mice. Int J Cancer 1998, 76:506-511.
    • (1998) Int J Cancer , vol.76 , pp. 506-511
    • Dondi, D.1    Moretti, R.M.2    Montagnani Marelli, M.3
  • 204
    • 0037289581 scopus 로고    scopus 로고
    • Signalling and anti-proliferative effects mediated by gonadotrophin-releasing hormone receptors after expression in prostate cancer cells using recombinant adenovirus
    • Franklin J., Hislop J., Flynn A., et al. Signalling and anti-proliferative effects mediated by gonadotrophin-releasing hormone receptors after expression in prostate cancer cells using recombinant adenovirus. J Endocrinol 2003, 176:275-284.
    • (2003) J Endocrinol , vol.176 , pp. 275-284
    • Franklin, J.1    Hislop, J.2    Flynn, A.3
  • 205
    • 0036554706 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone agonist limits DU-145 prostate cancer growth by attenuating epidermal growth factor receptor signaling
    • Wells A., Souto J.C., Solava J., et al. Luteinizing hormone-releasing hormone agonist limits DU-145 prostate cancer growth by attenuating epidermal growth factor receptor signaling. Clin Cancer Res 2002, 8:1251-1257.
    • (2002) Clin Cancer Res , vol.8 , pp. 1251-1257
    • Wells, A.1    Souto, J.C.2    Solava, J.3
  • 206
    • 67449152198 scopus 로고    scopus 로고
    • Gonadotropin releasing hormone analogs induce apoptosis by extrinsic pathway involving p53 phosphorylation in primary cell cultures of human prostatic adenocarcinomas
    • Clementi M., Sanchez C., Benitez D.A., et al. Gonadotropin releasing hormone analogs induce apoptosis by extrinsic pathway involving p53 phosphorylation in primary cell cultures of human prostatic adenocarcinomas. Prostate 2009, 69:1025-1033.
    • (2009) Prostate , vol.69 , pp. 1025-1033
    • Clementi, M.1    Sanchez, C.2    Benitez, D.A.3
  • 207
    • 33646475112 scopus 로고    scopus 로고
    • Effect of leuprolide and cetrorelix on cell growth, apoptosis, and GnRH receptor expression in primary cell cultures from human prostate carcinoma
    • Castellon E., Clementi M., Hitschfeld C., et al. Effect of leuprolide and cetrorelix on cell growth, apoptosis, and GnRH receptor expression in primary cell cultures from human prostate carcinoma. Cancer Invest 2006, 24:261-268.
    • (2006) Cancer Invest , vol.24 , pp. 261-268
    • Castellon, E.1    Clementi, M.2    Hitschfeld, C.3
  • 208
    • 33744485328 scopus 로고    scopus 로고
    • GnRH agonists and antagonists decrease the metastatic progression of human prostate cancer cell lines by inhibiting the plasminogen activator system
    • Dondi D., Festuccia C., Piccolella M., et al. GnRH agonists and antagonists decrease the metastatic progression of human prostate cancer cell lines by inhibiting the plasminogen activator system. Oncol Rep 2006, 15:393-400.
    • (2006) Oncol Rep , vol.15 , pp. 393-400
    • Dondi, D.1    Festuccia, C.2    Piccolella, M.3
  • 209
    • 29344450989 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone induces actin cytoskeleton remodeling and affects cell migration in a cell-type-specific manner in TSU-Pr1 and DU145 cells
    • Enomoto M., Utsumi M., Park M.K. Gonadotropin-releasing hormone induces actin cytoskeleton remodeling and affects cell migration in a cell-type-specific manner in TSU-Pr1 and DU145 cells. Endocrinology 2006, 147:530-542.
    • (2006) Endocrinology , vol.147 , pp. 530-542
    • Enomoto, M.1    Utsumi, M.2    Park, M.K.3
  • 210
    • 79851508522 scopus 로고    scopus 로고
    • Efficacy of a second line luteinizing hormone-releasing hormone agonist after advanced prostate cancer biochemical recurrence
    • Lawrentschuk N., Fernandes K., Bell D., et al. Efficacy of a second line luteinizing hormone-releasing hormone agonist after advanced prostate cancer biochemical recurrence. J Urol 2011, 185:848-854.
    • (2011) J Urol , vol.185 , pp. 848-854
    • Lawrentschuk, N.1    Fernandes, K.2    Bell, D.3
  • 211
    • 37549054715 scopus 로고    scopus 로고
    • Diversity of actions of GnRHs mediated by ligand-induced selective signaling
    • Millar R.P., Pawson A.J., Morgan K., et al. Diversity of actions of GnRHs mediated by ligand-induced selective signaling. Front Neuroendocrinol 2008, 29:17-35.
    • (2008) Front Neuroendocrinol , vol.29 , pp. 17-35
    • Millar, R.P.1    Pawson, A.J.2    Morgan, K.3
  • 212
    • 3843102580 scopus 로고    scopus 로고
    • Outside-in and inside-out signaling: the new concept that selectivity of ligand binding at the gonadotropin-releasing hormone receptor is modulated by the intracellular environment
    • Millar R.P., Pawson A.J. Outside-in and inside-out signaling: the new concept that selectivity of ligand binding at the gonadotropin-releasing hormone receptor is modulated by the intracellular environment. Endocrinology 2004, 145:3590-3593.
    • (2004) Endocrinology , vol.145 , pp. 3590-3593
    • Millar, R.P.1    Pawson, A.J.2
  • 213
    • 0030814022 scopus 로고    scopus 로고
    • Inhibition of growth of androgen-independent DU-145 prostate cancer in vivo by luteinising hormone-releasing hormone antagonist Cetrorelix and bombesin antagonists RC-3940-II and RC-3950-II
    • Jungwirth A., Pinski J., Galvan G., et al. Inhibition of growth of androgen-independent DU-145 prostate cancer in vivo by luteinising hormone-releasing hormone antagonist Cetrorelix and bombesin antagonists RC-3940-II and RC-3950-II. Eur J Cancer 1997, 33:1141-1148.
    • (1997) Eur J Cancer , vol.33 , pp. 1141-1148
    • Jungwirth, A.1    Pinski, J.2    Galvan, G.3
  • 214
    • 0030751523 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone antagonist Cetrorelix (SB-75) and bombesin antagonist RC-3940-II inhibit the growth of androgen-independent PC-3 prostate cancer in nude mice
    • Jungwirth A., Galvan G., Pinski J., et al. Luteinizing hormone-releasing hormone antagonist Cetrorelix (SB-75) and bombesin antagonist RC-3940-II inhibit the growth of androgen-independent PC-3 prostate cancer in nude mice. Prostate 1997, 32:164-172.
    • (1997) Prostate , vol.32 , pp. 164-172
    • Jungwirth, A.1    Galvan, G.2    Pinski, J.3
  • 215
    • 0032538353 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone (LH-RH) antagonist Cetrorelix inhibits growth of DU-145 human androgen-independent prostate carcinoma in nude mice and suppresses the levels and mRNA expression of IGF-II in tumors
    • Lamharzi N., Schally A.V., Koppan M. Luteinizing hormone-releasing hormone (LH-RH) antagonist Cetrorelix inhibits growth of DU-145 human androgen-independent prostate carcinoma in nude mice and suppresses the levels and mRNA expression of IGF-II in tumors. Regul Pept 1998, 77:185-192.
    • (1998) Regul Pept , vol.77 , pp. 185-192
    • Lamharzi, N.1    Schally, A.V.2    Koppan, M.3
  • 216
    • 84876422757 scopus 로고    scopus 로고
    • A switch from GnRH agonist to GnRH antagonist in castration-resistant prostate cancer patients leads to a low response rate on PSA
    • Masson-Lecomte A., Guy L., Pedron P., et al. A switch from GnRH agonist to GnRH antagonist in castration-resistant prostate cancer patients leads to a low response rate on PSA. World J Urol 2012, 10.1007/s00345-012-0841-1.
    • (2012) World J Urol
    • Masson-Lecomte, A.1    Guy, L.2    Pedron, P.3
  • 217
    • 4344633012 scopus 로고    scopus 로고
    • Antiproliferative effects of the GnRH antagonist cetrorelix and of GnRH-II on human endometrial and ovarian cancer cells are not mediated through the GnRH type I receptor
    • Grundker C., Schlotawa L., Viereck V., et al. Antiproliferative effects of the GnRH antagonist cetrorelix and of GnRH-II on human endometrial and ovarian cancer cells are not mediated through the GnRH type I receptor. Eur J Endocrinol 2004, 151:141-149.
    • (2004) Eur J Endocrinol , vol.151 , pp. 141-149
    • Grundker, C.1    Schlotawa, L.2    Viereck, V.3
  • 218
    • 35949003275 scopus 로고    scopus 로고
    • Expression of GnRH type II is regulated by the androgen receptor in prostate cancer
    • Darby S., Stockley J., Khan M.M., et al. Expression of GnRH type II is regulated by the androgen receptor in prostate cancer. Endocr Relat Cancer 2007, 14:613-624.
    • (2007) Endocr Relat Cancer , vol.14 , pp. 613-624
    • Darby, S.1    Stockley, J.2    Khan, M.M.3
  • 219
    • 23044486562 scopus 로고    scopus 로고
    • Differential effects of gonadotropin-releasing hormone (GnRH)-I and GnRH-II on prostate cancer cell signaling and death
    • Maiti K., Oh D.Y., Moon J.S., et al. Differential effects of gonadotropin-releasing hormone (GnRH)-I and GnRH-II on prostate cancer cell signaling and death. J Clin Endocrinol Metab 2005, 90:4287-4298.
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 4287-4298
    • Maiti, K.1    Oh, D.Y.2    Moon, J.S.3
  • 220
    • 59149089489 scopus 로고    scopus 로고
    • A gonadotropin-releasing hormone-II antagonist induces autophagy of prostate cancer cells
    • Kim D.K., Yang J.S., Maiti K., et al. A gonadotropin-releasing hormone-II antagonist induces autophagy of prostate cancer cells. Cancer Res 2009, 69:923-931.
    • (2009) Cancer Res , vol.69 , pp. 923-931
    • Kim, D.K.1    Yang, J.S.2    Maiti, K.3
  • 221
    • 10044239138 scopus 로고    scopus 로고
    • GnRH as a cell proliferation regulator: mechanism of action and evolutionary implications
    • Enomoto M., Park M.K. GnRH as a cell proliferation regulator: mechanism of action and evolutionary implications. Zoolog Sci 2004, 21:1005-1013.
    • (2004) Zoolog Sci , vol.21 , pp. 1005-1013
    • Enomoto, M.1    Park, M.K.2
  • 222
    • 0032797051 scopus 로고    scopus 로고
    • Cancer chemotherapy based on targeting of cytotoxic peptide conjugates to their receptors on tumors
    • Schally A.V., Nagy A. Cancer chemotherapy based on targeting of cytotoxic peptide conjugates to their receptors on tumors. Eur J Endocrinol 1999, 141:1-14.
    • (1999) Eur J Endocrinol , vol.141 , pp. 1-14
    • Schally, A.V.1    Nagy, A.2
  • 223
    • 0026503015 scopus 로고
    • Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups
    • Janaky T., Juhasz A., Bajusz S., et al. Analogues of luteinizing hormone-releasing hormone containing cytotoxic groups. Proc Natl Acad Sci USA 1992, 89:972-976.
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 972-976
    • Janaky, T.1    Juhasz, A.2    Bajusz, S.3
  • 224
    • 0027432237 scopus 로고
    • Inhibition of growth of experimental prostate cancer in rats by LH-RH analogs linked to cytotoxic radicals
    • Pinski J., Schally A.V., Yano T., et al. Inhibition of growth of experimental prostate cancer in rats by LH-RH analogs linked to cytotoxic radicals. Prostate 1993, 23:165-178.
    • (1993) Prostate , vol.23 , pp. 165-178
    • Pinski, J.1    Schally, A.V.2    Yano, T.3
  • 225
    • 8944225497 scopus 로고    scopus 로고
    • Cytotoxic analogs of luteinizing hormone-releasing hormone containing doxorubicin or 2-pyrrolinodoxorubicin, a derivative 500-1000 times more potent
    • Nagy A., Schally A.V., Armatis P., et al. Cytotoxic analogs of luteinizing hormone-releasing hormone containing doxorubicin or 2-pyrrolinodoxorubicin, a derivative 500-1000 times more potent. Proc Natl Acad Sci USA 1996, 93:7269-7273.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 7269-7273
    • Nagy, A.1    Schally, A.V.2    Armatis, P.3
  • 226
    • 0004608376 scopus 로고
    • Highly potent metallopeptide analogues of luteinizing hormone-releasing hormone
    • Bajusz S., Janaky T., Csernus V.J., et al. Highly potent metallopeptide analogues of luteinizing hormone-releasing hormone. Proc Natl Acad Sci USA 1989, 86:6313-6317.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 6313-6317
    • Bajusz, S.1    Janaky, T.2    Csernus, V.J.3
  • 227
    • 27144445244 scopus 로고    scopus 로고
    • Targeting of cytotoxic luteinizing hormone-releasing hormone analogs to breast, ovarian, endometrial, and prostate cancers
    • Nagy A., Schally A.V. Targeting of cytotoxic luteinizing hormone-releasing hormone analogs to breast, ovarian, endometrial, and prostate cancers. Biol Reprod 2005, 73:851-859.
    • (2005) Biol Reprod , vol.73 , pp. 851-859
    • Nagy, A.1    Schally, A.V.2
  • 228
    • 78650873834 scopus 로고    scopus 로고
    • Use of analogs of peptide hormones conjugated to cytotoxic radicals for chemotherapy targeted to receptors on tumors
    • Schally A.V., Engel J.B., Emons G., et al. Use of analogs of peptide hormones conjugated to cytotoxic radicals for chemotherapy targeted to receptors on tumors. Curr Drug Deliv 2011, 8:11-25.
    • (2011) Curr Drug Deliv , vol.8 , pp. 11-25
    • Schally, A.V.1    Engel, J.B.2    Emons, G.3
  • 229
    • 0030961688 scopus 로고    scopus 로고
    • Regression of rat Dunning R-3327-H prostate carcinoma by treatment with targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 containing 2-pyrrolinodoxorubicin
    • Jungwirth A., Schally A., Nagy A., et al. Regression of rat Dunning R-3327-H prostate carcinoma by treatment with targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 containing 2-pyrrolinodoxorubicin. Int J Oncol 1997, 10:877-884.
    • (1997) Int J Oncol , vol.10 , pp. 877-884
    • Jungwirth, A.1    Schally, A.2    Nagy, A.3
  • 230
    • 0032949187 scopus 로고    scopus 로고
    • Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits the growth of PC-82 human prostate cancer in nude mice
    • Koppan M., Nagy A., Schally A.V., et al. Targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207 inhibits the growth of PC-82 human prostate cancer in nude mice. Prostate 1999, 38:151-158.
    • (1999) Prostate , vol.38 , pp. 151-158
    • Koppan, M.1    Nagy, A.2    Schally, A.V.3
  • 231
    • 0037039710 scopus 로고    scopus 로고
    • Inhibition of in vivo proliferation of MDA-PCa-2b human prostate cancer by a targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207
    • Plonowski A., Schally A.V., Nagy A., et al. Inhibition of in vivo proliferation of MDA-PCa-2b human prostate cancer by a targeted cytotoxic analog of luteinizing hormone-releasing hormone AN-207. Cancer Lett 2002, 176:57-63.
    • (2002) Cancer Lett , vol.176 , pp. 57-63
    • Plonowski, A.1    Schally, A.V.2    Nagy, A.3
  • 232
    • 31944437524 scopus 로고    scopus 로고
    • Inhibition of human experimental prostate cancers by a targeted cytotoxic luteinizing hormone-releasing hormone analog AN-207
    • Stangelberger A., Schally A.V., Nagy A., et al. Inhibition of human experimental prostate cancers by a targeted cytotoxic luteinizing hormone-releasing hormone analog AN-207. Prostate 2006, 66:200-210.
    • (2006) Prostate , vol.66 , pp. 200-210
    • Stangelberger, A.1    Schally, A.V.2    Nagy, A.3
  • 233
    • 0141891453 scopus 로고    scopus 로고
    • Preclinical evaluation of targeted cytotoxic luteinizing hormone-releasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers
    • Letsch M., Schally A.V., Szepeshazi K., et al. Preclinical evaluation of targeted cytotoxic luteinizing hormone-releasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers. Clin Cancer Res 2003, 9:4505-4513.
    • (2003) Clin Cancer Res , vol.9 , pp. 4505-4513
    • Letsch, M.1    Schally, A.V.2    Szepeshazi, K.3
  • 234
    • 84861040329 scopus 로고    scopus 로고
    • AEZS-108: a targeted cytotoxic analog of LHRH for the treatment of cancers positive for LHRH receptors
    • Engel J., Emons G., Pinski J., et al. AEZS-108: a targeted cytotoxic analog of LHRH for the treatment of cancers positive for LHRH receptors. Expert Opin Investig Drugs 2012, 21:891-899.
    • (2012) Expert Opin Investig Drugs , vol.21 , pp. 891-899
    • Engel, J.1    Emons, G.2    Pinski, J.3
  • 235
    • 0034322411 scopus 로고    scopus 로고
    • Receptor mediated antiproliferative effects of the cytotoxic LHRH agonist AN-152 in human ovarian and endometrial cancer cell lines
    • Westphalen S., Kotulla G., Kaiser F., et al. Receptor mediated antiproliferative effects of the cytotoxic LHRH agonist AN-152 in human ovarian and endometrial cancer cell lines. Int J Oncol 2000, 17:1063-1069.
    • (2000) Int J Oncol , vol.17 , pp. 1063-1069
    • Westphalen, S.1    Kotulla, G.2    Kaiser, F.3
  • 236
    • 7044234874 scopus 로고    scopus 로고
    • Internalization of cytotoxic analog AN-152 of luteinizing hormone-releasing hormone induces apoptosis in human endometrial and ovarian cancer cell lines independent of multidrug resistance-1 (MDR-1) system
    • Gunthert A.R., Grundker C., Bongertz T., et al. Internalization of cytotoxic analog AN-152 of luteinizing hormone-releasing hormone induces apoptosis in human endometrial and ovarian cancer cell lines independent of multidrug resistance-1 (MDR-1) system. Am J Obstet Gynecol 2004, 191:1164-1172.
    • (2004) Am J Obstet Gynecol , vol.191 , pp. 1164-1172
    • Gunthert, A.R.1    Grundker, C.2    Bongertz, T.3
  • 237
    • 8644219704 scopus 로고    scopus 로고
    • Induction of apoptosis by AN-152, a cytotoxic analog of luteinizing hormone-releasing hormone (LHRH), in LHRH-R positive human breast cancer cells is independent of multidrug resistance-1 (MDR-1) system
    • Gunthert A.R., Grundker C., Bongertz T., et al. Induction of apoptosis by AN-152, a cytotoxic analog of luteinizing hormone-releasing hormone (LHRH), in LHRH-R positive human breast cancer cells is independent of multidrug resistance-1 (MDR-1) system. Breast Cancer Res Treat 2004, 87:255-264.
    • (2004) Breast Cancer Res Treat , vol.87 , pp. 255-264
    • Gunthert, A.R.1    Grundker, C.2    Bongertz, T.3
  • 238
    • 0034681171 scopus 로고    scopus 로고
    • Stability of cytotoxic luteinizing hormone-releasing hormone conjugate (AN-152) containing doxorubicin 14-O-hemiglutarate in mouse and human serum in vitro: implications for the design of preclinical studies
    • Nagy A., Plonowski A., Schally A.V. Stability of cytotoxic luteinizing hormone-releasing hormone conjugate (AN-152) containing doxorubicin 14-O-hemiglutarate in mouse and human serum in vitro: implications for the design of preclinical studies. Proc Natl Acad Sci USA 2000, 97:829-834.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 829-834
    • Nagy, A.1    Plonowski, A.2    Schally, A.V.3
  • 239
    • 0033674586 scopus 로고    scopus 로고
    • Cytotoxic luteinizing hormone-releasing hormone conjugates and their use in gynecological cancer therapy
    • Grundker C. Cytotoxic luteinizing hormone-releasing hormone conjugates and their use in gynecological cancer therapy. Eur J Endocrinol 2000, 143:569-572.
    • (2000) Eur J Endocrinol , vol.143 , pp. 569-572
    • Grundker, C.1
  • 240
    • 67649366372 scopus 로고    scopus 로고
    • Luteinizing hormone-releasing hormone receptor-targeted deslorelin-docetaxel conjugate enhances efficacy of docetaxel in prostate cancer therapy
    • Sundaram S., Durairaj C., Kadam R., et al. Luteinizing hormone-releasing hormone receptor-targeted deslorelin-docetaxel conjugate enhances efficacy of docetaxel in prostate cancer therapy. Mol Cancer Ther 2009, 8:1655-1665.
    • (2009) Mol Cancer Ther , vol.8 , pp. 1655-1665
    • Sundaram, S.1    Durairaj, C.2    Kadam, R.3
  • 241
    • 9844252335 scopus 로고    scopus 로고
    • Synthesis of gonadotropin-releasing hormone III analogs. Structure-antitumor activity relationships
    • Mezo I., Lovas S., Palyi I., et al. Synthesis of gonadotropin-releasing hormone III analogs. Structure-antitumor activity relationships. J Med Chem 1997, 40:3353-3358.
    • (1997) J Med Chem , vol.40 , pp. 3353-3358
    • Mezo, I.1    Lovas, S.2    Palyi, I.3
  • 242
    • 65249179433 scopus 로고    scopus 로고
    • Development of an oxime bond containing daunorubicin-gonadotropin-releasing hormone-III conjugate as a potential anticancer drug
    • Szabo I., Manea M., Orban E., et al. Development of an oxime bond containing daunorubicin-gonadotropin-releasing hormone-III conjugate as a potential anticancer drug. Bioconjug Chem 2009, 20:656-665.
    • (2009) Bioconjug Chem , vol.20 , pp. 656-665
    • Szabo, I.1    Manea, M.2    Orban, E.3
  • 243
    • 79960261391 scopus 로고    scopus 로고
    • In vitro degradation and antitumor activity of oxime bond-linked daunorubicin-GnRH-III bioconjugates and DNA-binding properties of daunorubicin-amino acid metabolites
    • Orban E., Mezo G., Schlage P., et al. In vitro degradation and antitumor activity of oxime bond-linked daunorubicin-GnRH-III bioconjugates and DNA-binding properties of daunorubicin-amino acid metabolites. Amino Acids 2011, 41:469-483.
    • (2011) Amino Acids , vol.41 , pp. 469-483
    • Orban, E.1    Mezo, G.2    Schlage, P.3
  • 244
    • 81255123473 scopus 로고    scopus 로고
    • Anthracycline-GnRH derivative bioconjugates with different linkages: synthesis, in vitro drug release and cytostatic effect
    • Schlage P., Mezo G., Orban E., et al. Anthracycline-GnRH derivative bioconjugates with different linkages: synthesis, in vitro drug release and cytostatic effect. J Control Release 2011, 156:170-178.
    • (2011) J Control Release , vol.156 , pp. 170-178
    • Schlage, P.1    Mezo, G.2    Orban, E.3
  • 245
    • 82555166976 scopus 로고    scopus 로고
    • In-vivo antitumour effect of daunorubicin-GnRH-III derivative conjugates on colon carcinoma-bearing mice
    • Manea M., Tovari J., Tejeda M., et al. In-vivo antitumour effect of daunorubicin-GnRH-III derivative conjugates on colon carcinoma-bearing mice. Anticancer Drugs 2012, 23:90-97.
    • (2012) Anticancer Drugs , vol.23 , pp. 90-97
    • Manea, M.1    Tovari, J.2    Tejeda, M.3
  • 246
    • 79960579138 scopus 로고    scopus 로고
    • Enhanced enzymatic stability and antitumor activity of daunorubicin-GnRH-III bioconjugates modified in position 4
    • Manea M., Leurs U., Orban E., et al. Enhanced enzymatic stability and antitumor activity of daunorubicin-GnRH-III bioconjugates modified in position 4. Bioconjug Chem 2011, 22:1320-1329.
    • (2011) Bioconjug Chem , vol.22 , pp. 1320-1329
    • Manea, M.1    Leurs, U.2    Orban, E.3
  • 247
    • 84865825675 scopus 로고    scopus 로고
    • Enhanced cellular uptake and in vitro antitumor activity of short-chain fatty acid acylated daunorubicin-GnRH-III bioconjugates
    • Hegedus R., Manea M., Orban E., et al. Enhanced cellular uptake and in vitro antitumor activity of short-chain fatty acid acylated daunorubicin-GnRH-III bioconjugates. Eur J Med Chem 2012, 56:155-165.
    • (2012) Eur J Med Chem , vol.56 , pp. 155-165
    • Hegedus, R.1    Manea, M.2    Orban, E.3
  • 248
    • 84860341182 scopus 로고    scopus 로고
    • GnRH-III based multifunctional drug delivery systems containing daunorubicin and methotrexate
    • Leurs U., Lajko E., Mezo G., et al. GnRH-III based multifunctional drug delivery systems containing daunorubicin and methotrexate. Eur J Med Chem 2012, 52:173-183.
    • (2012) Eur J Med Chem , vol.52 , pp. 173-183
    • Leurs, U.1    Lajko, E.2    Mezo, G.3
  • 249
    • 84860338337 scopus 로고    scopus 로고
    • Design, synthesis, in vitro stability and cytostatic effect of multifunctional anticancer drug-bioconjugates containing GnRH-III as a targeting moiety
    • Leurs U., Mezo G., Orban E., et al. Design, synthesis, in vitro stability and cytostatic effect of multifunctional anticancer drug-bioconjugates containing GnRH-III as a targeting moiety. Biopolymers 2012, 98:1-10.
    • (2012) Biopolymers , vol.98 , pp. 1-10
    • Leurs, U.1    Mezo, G.2    Orban, E.3
  • 250
    • 0033974530 scopus 로고    scopus 로고
    • Effects of the hinge region of cecropin A(1-8)-magainin 2(1-12), a synthetic antimicrobial peptide, on liposomes, bacterial and tumor cells
    • Shin S.Y., Kang J.H., Jang S.Y., et al. Effects of the hinge region of cecropin A(1-8)-magainin 2(1-12), a synthetic antimicrobial peptide, on liposomes, bacterial and tumor cells. Biochim Biophys Acta 2000, 1463:209-218.
    • (2000) Biochim Biophys Acta , vol.1463 , pp. 209-218
    • Shin, S.Y.1    Kang, J.H.2    Jang, S.Y.3
  • 251
    • 3042737827 scopus 로고    scopus 로고
    • Membrane disrupting lytic peptides for cancer treatments
    • Leuschner C., Hansel W. Membrane disrupting lytic peptides for cancer treatments. Curr Pharm Des 2004, 10:2299-2310.
    • (2004) Curr Pharm Des , vol.10 , pp. 2299-2310
    • Leuschner, C.1    Hansel, W.2
  • 252
    • 0043233155 scopus 로고    scopus 로고
    • Human prostate cancer cells and xenografts are targeted and destroyed through luteinizing hormone releasing hormone receptors
    • Leuschner C., Enright F.M., Gawronska-Kozak B., et al. Human prostate cancer cells and xenografts are targeted and destroyed through luteinizing hormone releasing hormone receptors. Prostate 2003, 56:239-249.
    • (2003) Prostate , vol.56 , pp. 239-249
    • Leuschner, C.1    Enright, F.M.2    Gawronska-Kozak, B.3
  • 253
    • 33947603270 scopus 로고    scopus 로고
    • Conjugates of lytic peptides and LHRH or betaCG target and cause necrosis of prostate cancers and metastases
    • Hansel W., Leuschner C., Enright F. Conjugates of lytic peptides and LHRH or betaCG target and cause necrosis of prostate cancers and metastases. Mol Cell Endocrinol 2007, 269:26-33.
    • (2007) Mol Cell Endocrinol , vol.269 , pp. 26-33
    • Hansel, W.1    Leuschner, C.2    Enright, F.3
  • 254
    • 78549244732 scopus 로고    scopus 로고
    • LHRH-conjugated lytic peptides directly target prostate cancer cells
    • Yates C., Sharp S., Jones J., et al. LHRH-conjugated lytic peptides directly target prostate cancer cells. Biochem Pharmacol 2011, 81:104-110.
    • (2011) Biochem Pharmacol , vol.81 , pp. 104-110
    • Yates, C.1    Sharp, S.2    Jones, J.3
  • 255
    • 0347478040 scopus 로고    scopus 로고
    • GnRH-PAP hormonotoxin targets cytotoxicity to prostate cancer cell lines
    • Qi L., Nett T.M., Allen M.C., et al. GnRH-PAP hormonotoxin targets cytotoxicity to prostate cancer cell lines. Urol Res 2003, 31:374-377.
    • (2003) Urol Res , vol.31 , pp. 374-377
    • Qi, L.1    Nett, T.M.2    Allen, M.C.3
  • 256
    • 0037390439 scopus 로고    scopus 로고
    • Cytotoxic activity of gonadotropin-releasing hormone (GnRH)-pokeweed antiviral protein conjugates in cell lines expressing GnRH receptors
    • Yang W.H., Wieczorck M., Allen M.C., et al. Cytotoxic activity of gonadotropin-releasing hormone (GnRH)-pokeweed antiviral protein conjugates in cell lines expressing GnRH receptors. Endocrinology 2003, 144:1456-1463.
    • (2003) Endocrinology , vol.144 , pp. 1456-1463
    • Yang, W.H.1    Wieczorck, M.2    Allen, M.C.3
  • 257
    • 1542615080 scopus 로고    scopus 로고
    • Binding and cytotoxicity of conjugated and recombinant fusion proteins targeted to the gonadotropin-releasing hormone receptor
    • Qi L., Nett T.M., Allen M.C., et al. Binding and cytotoxicity of conjugated and recombinant fusion proteins targeted to the gonadotropin-releasing hormone receptor. Cancer Res 2004, 64:2090-2095.
    • (2004) Cancer Res , vol.64 , pp. 2090-2095
    • Qi, L.1    Nett, T.M.2    Allen, M.C.3


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