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Volumn 46, Issue 1, 2015, Pages 243-253

Oxime bond-linked daunorubicin-GnRH-III bioconjugates exert antitumor activity in castration-resistant prostate cancer cells via the type i GnRH receptor

Author keywords

Castrationresistant prostate cancer; Daunorubicin; Daunorubicin GnRH III bioconjugates; GnRH III; Gonadotropin releasing hormone receptor

Indexed keywords

ANTINEOPLASTIC AGENT; DAUNORUBICIN; GNRHR PROTEIN, HUMAN; GONADORELIN; GONADORELIN RECEPTOR; GONADOTROPIN-RELEASING HORMONE-III; OXIME; PYROGLUTAMIC ACID;

EID: 84917706541     PISSN: 10196439     EISSN: 17912423     Source Type: Journal    
DOI: 10.3892/ijo.2014.2730     Document Type: Article
Times cited : (15)

References (40)
  • 2
    • 4143134065 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptors: Structure, expression, and signaling transduction
    • Kakar SS, Malik MT, Winters SJ and Mazhawidza W: Gonadotropin-releasing hormone receptors: structure, expression, and signaling transduction. Vitam Horm 69: 151-207, 2004.
    • (2004) Vitam Horm , vol.69 , pp. 151-207
    • Kakar, S.S.1    Malik, M.T.2    Winters, S.J.3    Mazhawidza, W.4
  • 3
    • 24044447902 scopus 로고    scopus 로고
    • GnRHs and GnRH receptors
    • Millar RP: GnRHs and GnRH receptors. Anim Reprod Sci 88: 5-28, 2005.
    • (2005) Anim Reprod Sci , vol.88 , pp. 5-28
    • Millar, R.P.1
  • 4
    • 0028235123 scopus 로고
    • The use of luteinizing hormone releasing hormone agonists and antagonists in gynaecological cancers
    • Emons G and Schally AV: The use of luteinizing hormone releasing hormone agonists and antagonists in gynaecological cancers. Hum Reprod 9: 1364-1379, 1994.
    • (1994) Hum Reprod , vol.9 , pp. 1364-1379
    • Emons, G.1    Schally, A.V.2
  • 5
    • 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 26: 361-379, 2005.
    • (2005) Endocr Rev , vol.26 , pp. 361-379
    • Labrie, F.1    Belanger, A.2    Luu-The, V.3
  • 6
    • 0033630476 scopus 로고    scopus 로고
    • GnRH receptor and apoptotic signaling
    • Imai A and Tamaya T: GnRH receptor and apoptotic signaling. Vitam Horm 59: 1-33, 2000.
    • (2000) Vitam Horm , vol.59 , pp. 1-33
    • Imai, A.1    Tamaya, T.2
  • 7
    • 0036164170 scopus 로고    scopus 로고
    • Biology of the gonadotropin-releasing hormone system in gynecological cancers
    • Grundker C, Gunthert AR, Westphalen S and Emons G: Biology of the gonadotropin-releasing hormone system in gynecological cancers. Eur J Endocrinol 146: 1-14, 2002.
    • (2002) Eur J Endocrinol , vol.146 , pp. 1-14
    • Grundker, C.1    Gunthert, A.R.2    Westphalen, S.3    Emons, G.4
  • 8
    • 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?
    • Montagnani Marelli M, Moretti RM, Januszkiewicz-Caulier J, Motta M and Limonta P: Gonadotropin-releasing hormone (GnRH) receptors in tumors: a new rationale for the therapeutical application of GnRH analogs in cancer patients? Curr Cancer Drug Targets 6: 257-269, 2006.
    • (2006) Curr Cancer Drug Targets , vol.6 , pp. 257-269
    • Montagnani Marelli, M.1    Moretti, R.M.2    Januszkiewicz-Caulier, J.3    Motta, M.4    Limonta, P.5
  • 10
    • 84878921940 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone receptors as molecular therapeutic targets in prostate cancer: Current options and emerging strategies
    • Limonta P and Manea M: Gonadotropin-releasing hormone receptors as molecular therapeutic targets in prostate cancer: Current options and emerging strategies. Cancer Treat Rev 39: 647-663, 2013.
    • (2013) Cancer Treat Rev , vol.39 , pp. 647-663
    • Limonta, P.1    Manea, M.2
  • 11
    • 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 and Schally AV: AEZS-108 : a targeted cytotoxic analog of LHRH for the treatment of cancers positive for LHRH receptors. Expert Opin Investig Drugs 21: 891-899, 2012.
    • (2012) Expert Opin Investig Drugs , vol.21 , pp. 891-899
    • Engel, J.1    Emons, G.2    Pinski, J.3    Schally, A.V.4
  • 12
    • 0036668076 scopus 로고    scopus 로고
    • Lamprey gonadotropin hormone-releasing hormone-III has no selective follicle-stimulating hormonereleasing effect in rats
    • Kovacs M, Seprodi J, Koppan M, Horvath JE, Vincze B, Teplan I and Flerko B: Lamprey gonadotropin hormone-releasing hormone-III has no selective follicle-stimulating hormonereleasing effect in rats. J Neuroendocrinol 14: 647-655, 2002.
    • (2002) J Neuroendocrinol , vol.14 , pp. 647-655
    • Kovacs, M.1    Seprodi, J.2    Koppan, M.3    Horvath, J.E.4    Vincze, B.5    Teplan, I.6    Flerko, B.7
  • 13
    • 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 20: 656-665, 2009.
    • (2009) Bioconjug Chem , vol.20 , pp. 656-665
    • Szabo, I.1    Manea, M.2    Orban, E.3
  • 14
    • 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 22: 1320-1329, 2011.
    • (2011) Bioconjug Chem , vol.22 , pp. 1320-1329
    • Manea, M.1    Leurs, U.2    Orban, E.3
  • 15
    • 79960261391 scopus 로고    scopus 로고
    • In vitro degradation and antitumor activity of oxime bond-linked daunorubicin-GnRH-III bioconjugates and DNA-binding properties of daunorubicinamino 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 daunorubicinamino acid metabolites. Amino Acids 41: 469-483, 2011.
    • (2011) Amino Acids , vol.41 , pp. 469-483
    • Orban, E.1    Mezo, G.2    Schlage, P.3
  • 16
    • 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, Bosze S and Manea M: Anthracycline-GnRH derivative bioconjugates with different linkages: synthesis, in vitro drug release and cytostatic effect. J Control Release 156: 170-178, 2011.
    • (2011) J Control Release , vol.156 , pp. 170-178
    • Schlage, P.1    Mezo, G.2    Orban, E.3    Bosze, S.4    Manea, M.5
  • 18
    • 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 102: 51-56, 2011.
    • (2011) Cancer Sci , vol.102 , pp. 51-56
    • Akaza, H.1
  • 19
    • 84865472321 scopus 로고    scopus 로고
    • Management of castration-resistant prostate cancer: A call to urologists
    • Fitzpatrick JM: Management of castration-resistant prostate cancer: a call to urologists. BJU Int 110: 772-774, 2012.
    • (2012) BJU Int , vol.110 , pp. 772-774
    • Fitzpatrick, J.M.1
  • 20
    • 84858441614 scopus 로고    scopus 로고
    • Novel therapeutics for the management of castration-resistant prostate cancer (CRPC)
    • Lee DJ, Cha EK, Dubin JM, et al: Novel therapeutics for the management of castration-resistant prostate cancer (CRPC). BJU Int 109: 968-985, 2012.
    • (2012) BJU Int , vol.109 , pp. 968-985
    • Lee, D.J.1    Cha, E.K.2    Dubin, J.M.3
  • 21
    • 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 RM, Montagnani Marelli M, Garattini E and Motta M: 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 54: 4091-4095, 1994.
    • (1994) Cancer Res , vol.54 , pp. 4091-4095
    • Dondi, D.1    Limonta, P.2    Moretti, R.M.3    Montagnani Marelli, M.4    Garattini, E.5    Motta, M.6
  • 22
    • 0031960297 scopus 로고    scopus 로고
    • Growthinhibitory effects of luteinizing hormone-releasing hormone (LHRH) agonists on xenografts of the du 145 human androgenindependent prostate cancer cell line in nude mice
    • Dondi D, Moretti RM, Montagnani Marelli M, et al: Growthinhibitory effects of luteinizing hormone-releasing hormone (LHRH) agonists on xenografts of the DU 145 human androgenindependent prostate cancer cell line in nude mice. Int J Cancer 76: 506-511, 1998.
    • (1998) Int J Cancer , vol.76 , pp. 506-511
    • Dondi, D.1    Moretti, R.M.2    Montagnani Marelli, M.3
  • 23
    • 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 RM, Montagnani Marelli M, Dondi D, Parenti M and Motta M: The luteinizing hormone-releasing hormone receptor in human prostate cancer cells: messenger ribonucleic acid expression, molecular size, and signal transduction pathway. Endocrinology 140: 5250-5256, 1999.
    • (1999) Endocrinology , vol.140 , pp. 5250-5256
    • Limonta, P.1    Moretti, R.M.2    Montagnani Marelli, M.3    Dondi, D.4    Parenti, M.5    Motta, M.6
  • 24
    • 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 RM, Mai S, Procacci P and Limonta P: 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 30: 261-271, 2007.
    • (2007) Int J Oncol , vol.30 , pp. 261-271
    • Montagnani Marelli, M.1    Moretti, R.M.2    Mai, S.3    Procacci, P.4    Limonta, P.5
  • 26
    • 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 VJ, Darby S, Khan MM, Lock WG, Robson CN and Leung HY: Evidence that prostate gonadotropin-releasing hormone receptors mediate an anti-tumourigenic response to analogue therapy in hormone refractory prostate cancer. J Pathol 206: 205-213, 2005.
    • (2005) J Pathol , vol.206 , pp. 205-213
    • Gnanapragasam, V.J.1    Darby, S.2    Khan, M.M.3    Lock, W.G.4    Robson, C.N.5    Leung, H.Y.6
  • 27
    • 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 SV, Schally AV, 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 16: 4675-4680, 2010.
    • (2010) Clin Cancer Res , vol.16 , pp. 4675-4680
    • Liu, S.V.1    Schally, A.V.2    Hawes, D.3
  • 28
    • 13044272900 scopus 로고    scopus 로고
    • Gonadotropin-releasing hormone analogue conjugates with strong selective antitumor activity
    • Palyi I, Vincze B, Lovas S, et al: Gonadotropin-releasing hormone analogue conjugates with strong selective antitumor activity. Proc Natl Acad Sci USA 96: 2361-2366, 1999.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 2361-2366
    • Palyi, I.1    Vincze, B.2    Lovas, S.3
  • 29
    • 84898843293 scopus 로고    scopus 로고
    • NVP-BEZ235, a dual PI3K/mTOR inhibitor, induces cell death through alternate routes in prostate cancer cells depending on the PTEN genotype
    • Hong SW, Shin JS, Moon JH, et al: NVP-BEZ235, a dual PI3K/mTOR inhibitor, induces cell death through alternate routes in prostate cancer cells depending on the PTEN genotype. Apoptosis 19: 895-904, 2014.
    • (2014) Apoptosis , vol.19 , pp. 895-904
    • Hong, S.W.1    Shin, J.S.2    Moon, J.H.3
  • 30
    • 84864422677 scopus 로고    scopus 로고
    • Targeted chemotherapy of endometrial, ovarian and breast cancers with cytotoxic analogs of luteinizing hormonereleasing hormone (LHRH)
    • Engel JB, Schally AV, Buchholz S, Seitz S, Emons G and Ortmann O: Targeted chemotherapy of endometrial, ovarian and breast cancers with cytotoxic analogs of luteinizing hormonereleasing hormone (LHRH). Arch Gynecol Obstet 286: 437-442, 2012.
    • (2012) Arch Gynecol Obstet , vol.286 , pp. 437-442
    • Engel, J.B.1    Schally, A.V.2    Buchholz, S.3    Seitz, S.4    Emons, G.5    Ortmann, O.6
  • 31
    • 84893797792 scopus 로고    scopus 로고
    • Efficacy and safety of AEZS-108 (LHRH agonist linked to doxorubicin) in women with advanced or recurrent endometrial cancer expressing LHRH receptors: A multicenter phase 2 trial (AGO-GYN5)
    • Emons G, Gorchev G, Harter P, et al: Efficacy and safety of AEZS-108 (LHRH agonist linked to doxorubicin) in women with advanced or recurrent endometrial cancer expressing LHRH receptors: a multicenter phase 2 trial (AGO-GYN5). Int J Gynecol Cancer 24: 260-265, 2014.
    • (2014) Int J Gynecol Cancer , vol.24 , pp. 260-265
    • Emons, G.1    Gorchev, G.2    Harter, P.3
  • 32
    • 84868626417 scopus 로고    scopus 로고
    • Receptor-targeted therapy of human experimental urinary bladder cancers with cytotoxic LH-RH analog AN-152 [AEZS-108]
    • Szepeshazi K, Schally AV, Keller G, et al: Receptor-targeted therapy of human experimental urinary bladder cancers with cytotoxic LH-RH analog AN-152 [AEZS-108]. Oncotarget 3: 686-699, 2012.
    • (2012) Oncotarget , vol.3 , pp. 686-699
    • Szepeshazi, K.1    Schally, A.V.2    Keller, G.3
  • 33
    • 84879011680 scopus 로고    scopus 로고
    • Inhibition of U-87 MG glioblastoma by AN-152 (AEZS-108), a targeted cytotoxic analog of luteinizing hormone-releasing hormone
    • Jaszberenyi M, Schally AV, Block NL, Nadji M, Vidaurre I, Szalontay L and Rick FG: Inhibition of U-87 MG glioblastoma by AN-152 (AEZS-108), a targeted cytotoxic analog of luteinizing hormone-releasing hormone. Oncotarget 4: 422-432, 2013.
    • (2013) Oncotarget , vol.4 , pp. 422-432
    • Jaszberenyi, M.1    Schally, A.V.2    Block, N.L.3    Nadji, M.4    Vidaurre, I.5    Szalontay, L.6    Rick, F.G.7
  • 34
    • 84880313248 scopus 로고    scopus 로고
    • Powerful inhibition of experimental human pancreatic cancers by receptor targeted cytotoxic LH-RH analog AEZS-108
    • Szepeshazi K, Schally AV, Block NL, et al: Powerful inhibition of experimental human pancreatic cancers by receptor targeted cytotoxic LH-RH analog AEZS-108. Oncotarget 4: 751-760, 2013.
    • (2013) Oncotarget , vol.4 , pp. 751-760
    • Szepeshazi, K.1    Schally, A.V.2    Block, N.L.3
  • 35
    • 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, Schulcz A, Kapuvari B, Vincze B and Mezo G: In-vivo antitumour effect of daunorubicin- GnRH-III derivative conjugates on colon carcinoma-bearing mice. Anticancer Drugs 23: 90-97, 2012.
    • (2012) Anticancer Drugs , vol.23 , pp. 90-97
    • Manea, M.1    Tovari, J.2    Tejeda, M.3    Schulcz, A.4    Kapuvari, B.5    Vincze, B.6    Mezo, G.7
  • 36
    • 0141891453 scopus 로고    scopus 로고
    • Preclinical evaluation of targeted cytotoxic luteinizing hormonereleasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers
    • Letsch M, Schally AV, Szepeshazi K, Halmos G and Nagy A: Preclinical evaluation of targeted cytotoxic luteinizing hormonereleasing hormone analogue AN-152 in androgen-sensitive and insensitive prostate cancers. Clin Cancer Res 9: 4505-4513, 2003.
    • (2003) Clin Cancer Res , vol.9 , pp. 4505-4513
    • Letsch, M.1    Schally, A.V.2    Szepeshazi, K.3    Halmos, G.4    Nagy, A.5
  • 37
    • 84898994548 scopus 로고    scopus 로고
    • GnRH-gemcitabine conjugates for the treatment of androgen-independent prostate cancer: Pharmacokinetic enhancements combined with targeted drug delivery
    • Karampelas T, Argyros O, Sayyad N, et al: GnRH-gemcitabine conjugates for the treatment of androgen-independent prostate cancer: pharmacokinetic enhancements combined with targeted drug delivery. Bioconjug Chem 25: 813-823, 2014.
    • (2014) Bioconjug Chem , vol.25 , pp. 813-823
    • Karampelas, T.1    Argyros, O.2    Sayyad, N.3
  • 38
    • 84865825675 scopus 로고    scopus 로고
    • Enhanced cellular uptake and in vitro antitumor activity of short-chain fatty acid acylated daunorubicin-GnRH-III bioconjugates
    • Hegedüs R, Manea M, Orbán 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 56: 155-165, 2012.
    • (2012) Eur J Med Chem , vol.56 , pp. 155-165
    • Hegedüs, R.1    Manea, M.2    Orbán, E.3
  • 39
    • 17044397637 scopus 로고    scopus 로고
    • Molecular biology of gonadotropinreleasing hormone (GnRH)-I. GnRH-II, and their receptors in humans
    • Cheng CK and Leung PC: Molecular biology of gonadotropinreleasing hormone (GnRH)-I, GnRH-II, and their receptors in humans. Endocr Rev 26: 283-306, 2005.
    • (2005) Endocr Rev , vol.26 , pp. 283-306
    • Cheng, C.K.1    Leung, P.C.2
  • 40
    • 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 52: 173-183, 2012.
    • (2012) Eur J Med Chem , vol.52 , pp. 173-183
    • Leurs, U.1    Lajko, E.2    Mezo, G.3


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