메뉴 건너뛰기




Volumn 31, Issue 6, 2004, Pages 691-698

Impact on estrogen receptor binding and target tissue uptake of [ 18F]fluorine substitution at the 16α-position of fulvestrant (Faslodex; ICI 182,780)

Author keywords

Antiestrogen therapy; Breast cancer; Estrogen receptor; Fluor 18; PET; Positron emission tomography; Radiopharmaceutical

Indexed keywords

ESTROGEN RECEPTOR; FLUORINE 18; FULVESTRANT;

EID: 3042753367     PISSN: 09698051     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nucmedbio.2004.02.010     Document Type: Article
Times cited : (30)

References (40)
  • 1
    • 0018219234 scopus 로고
    • Hormone receptors: Their role in predicting prognosis and response to endocrine therapy
    • McGuire W.L. Hormone receptors Their role in predicting prognosis and response to endocrine therapy. Semin Oncol. 5:1978;428-433
    • (1978) Semin Oncol , vol.5 , pp. 428-433
    • McGuire, W.L.1
  • 2
    • 0030333304 scopus 로고    scopus 로고
    • Epidemiology of susceptibility to breast cancer
    • Hulka B.S. Epidemiology of susceptibility to breast cancer. Prog Clin Biol Res. 395:1996;289-295
    • (1996) Prog Clin Biol Res , vol.395 , pp. 289-295
    • Hulka, B.S.1
  • 4
    • 0035344623 scopus 로고    scopus 로고
    • Systemic treatment of metastatic breast cancer
    • Johnston S.R. Systemic treatment of metastatic breast cancer. Hosp Med. 62:2001;289-295
    • (2001) Hosp Med , vol.62 , pp. 289-295
    • Johnston, S.R.1
  • 5
    • 0038243777 scopus 로고    scopus 로고
    • Update on the current use of hormonals as therapy in advanced breast cancer
    • Vogel C.L. Update on the current use of hormonals as therapy in advanced breast cancer. Anticancer Drugs. 14:2003;265-273
    • (2003) Anticancer Drugs , vol.14 , pp. 265-273
    • Vogel, C.L.1
  • 6
    • 0033791553 scopus 로고    scopus 로고
    • Tamoxifen's clinical applications: Old and new
    • Buzdar A.U. Tamoxifen's clinical applications old and new. Arch Family Med. 9:2000;906-912
    • (2000) Arch Family Med , vol.9 , pp. 906-912
    • Buzdar, A.U.1
  • 7
    • 0034984594 scopus 로고    scopus 로고
    • Endocrine therapy in the treatment of metastatic breast cancer
    • Buzdar A.U. Endocrine therapy in the treatment of metastatic breast cancer. Sem Oncol. 28:2001;291-304
    • (2001) Sem Oncol , vol.28 , pp. 291-304
    • Buzdar, A.U.1
  • 9
    • 0028208456 scopus 로고
    • Endometrial cancer in tamoxifen-treated breast cancer patients: Findings from the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-14
    • Fisher B., Costantino J.P., Redmond C.K., Fisher E.R., Wickerham D.L., Cronin W.M. Endometrial cancer in tamoxifen-treated breast cancer patients Findings from the National Surgical Adjuvant Breast and Bowel Project (NSABP) B-14. J Natl Cancer Inst. 86:1994;527-537
    • (1994) J Natl Cancer Inst , vol.86 , pp. 527-537
    • Fisher, B.1    Costantino, J.P.2    Redmond, C.K.3    Fisher, E.R.4    Wickerham, D.L.5    Cronin, W.M.6
  • 10
    • 0027758638 scopus 로고
    • Drug resistance to tamoxifen during breast cancer therapy
    • Wolf D.M., Jordan V.C., William L. Drug resistance to tamoxifen during breast cancer therapy. Breast Cancer Res Treat. 27:1993;27-40
    • (1993) Breast Cancer Res Treat , vol.27 , pp. 27-40
    • Wolf, D.M.1    Jordan, V.C.2    William, L.3
  • 11
    • 0037435046 scopus 로고    scopus 로고
    • Antiestrogens and selective estrogen receptor modulators as multifunctional medicines. 1. Receptor interactions
    • Jordan V.C. Antiestrogens and selective estrogen receptor modulators as multifunctional medicines. 1. Receptor interactions. J Med Chem. 46:2003;883-908
    • (2003) J Med Chem , vol.46 , pp. 883-908
    • Jordan, V.C.1
  • 12
    • 0037468902 scopus 로고    scopus 로고
    • Antiestrogens and selective estrogen receptor modulators as multifunctional medicines. 2. Clinical considerations and new agents
    • Jordan V.C. Antiestrogens and selective estrogen receptor modulators as multifunctional medicines. 2. Clinical considerations and new agents. J Med Chem. 46:2003;1081-1111
    • (2003) J Med Chem , vol.46 , pp. 1081-1111
    • Jordan, V.C.1
  • 13
    • 0035464108 scopus 로고    scopus 로고
    • Aromatase, aromatase inhibitors, and breast cancer
    • Brueggemeier R.W. Aromatase, aromatase inhibitors, and breast cancer. Am J Therapeutics. 8:2001;333-344
    • (2001) Am J Therapeutics , vol.8 , pp. 333-344
    • Brueggemeier, R.W.1
  • 14
    • 0002149652 scopus 로고    scopus 로고
    • Antiaromatase agents: Preclinical data and neoadjuvant therapy
    • Miller W.R., Dixon J.M. Antiaromatase agents Preclinical data and neoadjuvant therapy. Clin. Breast Cancer. 1:2000;S9-14
    • (2000) Clin. Breast Cancer , vol.1 , pp. 9-14
    • Miller, W.R.1    Dixon, J.M.2
  • 15
    • 0026395885 scopus 로고
    • A potent specific pure antiestrogen with clinical potential
    • Wakeling A.E., Dukes M., Bowler J. A potent specific pure antiestrogen with clinical potential. Cancer Res. 51:1991;3867-3873
    • (1991) Cancer Res , vol.51 , pp. 3867-3873
    • Wakeling, A.E.1    Dukes, M.2    Bowler, J.3
  • 16
    • 0028267222 scopus 로고
    • Anti-proliferative and antiestrogenic effects of ICI 164,384 and ICI 182,780 in 4-OH-tamoxifen resistant human breast-cancer cells
    • Coopman P., Garcia M., Brünner N., Derocq D., Clarke R., Rochefort H. Anti-proliferative and antiestrogenic effects of ICI 164, 384 and ICI 182, 780 in 4-OH-tamoxifen resistant human breast-cancer cells. Int J Cancer. 56:1994;295-300
    • (1994) Int J Cancer , vol.56 , pp. 295-300
    • Coopman, P.1    Garcia, M.2    Brünner, N.3    Derocq, D.4    Clarke, R.5    Rochefort, H.6
  • 17
    • 0036778135 scopus 로고    scopus 로고
    • A new estrogen receptor antagonist - An overview of available data
    • Jones S.E. A new estrogen receptor antagonist - an overview of available data. Breast Cancer Res Treat. 75:2002;S19-21
    • (2002) Breast Cancer Res Treat , vol.75 , pp. 19-21
    • Jones, S.E.1
  • 18
    • 0036998677 scopus 로고    scopus 로고
    • Fulvestrant (′Faslodex') - A new treatment option for patients progressing on prior endocrine therapy
    • Morris C., Wakeling A.E. Fulvestrant (′Faslodex') - a new treatment option for patients progressing on prior endocrine therapy. Endocrine-Related Cancer. 9:2002;267-276
    • (2002) Endocrine-Related Cancer , vol.9 , pp. 267-276
    • Morris, C.1    Wakeling, A.E.2
  • 20
    • 0025084510 scopus 로고
    • Inhibition of estrogen receptor-DNA binding by the 'pure' antiestrogen ICI 164,384 appears to be mediated by impaired receptor dimerization
    • Fawell S.E., White R., Hoare S., Sydenham M., Page M., Parker M.G. Inhibition of estrogen receptor-DNA binding by the 'pure' antiestrogen ICI 164, 384 appears to be mediated by impaired receptor dimerization. Proc Natl Acad Sci USA. 87:1990;6883-6887
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 6883-6887
    • Fawell, S.E.1    White, R.2    Hoare, S.3    Sydenham, M.4    Page, M.5    Parker, M.G.6
  • 21
    • 0026560435 scopus 로고
    • Antiestrogen ICI 164,384 reduces cellular estrogen content by increasing its turnover
    • Dauvois S., Daniellan P.S., White R., Parker M.G. Antiestrogen ICI 164, 384 reduces cellular estrogen content by increasing its turnover. Proc Natl Acad Sci USA. 89:1992;4037-4041
    • (1992) Proc Natl Acad Sci USA , vol.89 , pp. 4037-4041
    • Dauvois, S.1    Daniellan, P.S.2    White, R.3    Parker, M.G.4
  • 22
    • 0027768899 scopus 로고
    • The antiestrogen ICI 182,780 disrupts estrogen receptor nucleocytoplasmic shuttling
    • Dauvois S., White R., Parker M.G. The antiestrogen ICI 182, 780 disrupts estrogen receptor nucleocytoplasmic shuttling. J Cell Sci. 106:1993;1377-1388
    • (1993) J Cell Sci , vol.106 , pp. 1377-1388
    • Dauvois, S.1    White, R.2    Parker, M.G.3
  • 23
    • 0027179615 scopus 로고
    • Action of pure antiestrogens in inhibiting estrogen receptor function
    • Parker M.G. Action of pure antiestrogens in inhibiting estrogen receptor function. Breast Cancer Res Treat. 26:1993;131-137
    • (1993) Breast Cancer Res Treat , vol.26 , pp. 131-137
    • Parker, M.G.1
  • 24
    • 0019157188 scopus 로고
    • Estrogen-receptor binding and biologic activity of tamoxifen and its metabolites
    • Wakeling A.E., Slater S.R. Estrogen-receptor binding and biologic activity of tamoxifen and its metabolites. Cancer Treat Rep. 64:1980;741-744
    • (1980) Cancer Treat Rep , vol.64 , pp. 741-744
    • Wakeling, A.E.1    Slater, S.R.2
  • 25
    • 0001251243 scopus 로고
    • Synthesis of nca 7α-(11-[18F]fluoroundecyl)-estradiol: Evaluation of a vector for estrogen receptor based agents
    • DaSilva J.N., Crouzel C., van Lier J.E. Synthesis of nca 7α-(11-[18F]fluoroundecyl)-estradiol Evaluation of a vector for estrogen receptor based agents. J Label Compd Radiopharm. 26:1989;342S-343S
    • (1989) J Label Compd Radiopharm , vol.26
    • Dasilva, J.N.1    Crouzel, C.2    Van Lier, J.E.3
  • 26
    • 0025055583 scopus 로고
    • Synthesis and structure-affinity of a series of 7α-undecylestradiol derivatives: A potential vector for therapy and imaging of estrogen receptor-positive cancers
    • DaSilva J.N., van Lier J.E. Synthesis and structure-affinity of a series of 7α-undecylestradiol derivatives A potential vector for therapy and imaging of estrogen receptor-positive cancers. J Med Chem. 33:1990;430-434
    • (1990) J Med Chem , vol.33 , pp. 430-434
    • Dasilva, J.N.1    Van Lier, J.E.2
  • 27
    • 0025115841 scopus 로고
    • 125I]iodophenoxy) undecyl]-17β-estradiol: A potent vector for therapy of adrenal and estrogen receptor-positive cancers
    • 125I]iodophenoxy)undecyl]-17β-estradiol A potent vector for therapy of adrenal and estrogen receptor-positive cancers. J Steroid Biochem Mol Biol. 37:1990;77-83
    • (1990) J Steroid Biochem Mol Biol , vol.37 , pp. 77-83
    • Dasilva, J.N.1    Van Lier, J.E.2
  • 28
    • 0021734833 scopus 로고
    • Synthesis of 16-fluoroestrogens by unusually facile fluoride ion displacement reactions: Prospects for the preparation of fluorine-18 labeled estrogens
    • Kiesewetter D.O., Katzenellenbogen J.A., Kilbourn M.R., Welch M.J. Synthesis of 16-fluoroestrogens by unusually facile fluoride ion displacement reactions Prospects for the preparation of fluorine-18 labeled estrogens. J. Org. Chem. 49:1984;4900-4905
    • (1984) J. Org. Chem. , vol.49 , pp. 4900-4905
    • Kiesewetter, D.O.1    Katzenellenbogen, J.A.2    Kilbourn, M.R.3    Welch, M.J.4
  • 30
    • 0028361392 scopus 로고
    • Preparation of [18F]16α-fluoro-17β-estradiol by selective nucleophilic substitution
    • Lim J.L., Berridge M.S., Tewson T.J. Preparation of [18F]16α- fluoro-17β-estradiol by selective nucleophilic substitution. J Label Compd Radiopharm. 35:1994;176-177
    • (1994) J Label Compd Radiopharm , vol.35 , pp. 176-177
    • Lim, J.L.1    Berridge, M.S.2    Tewson, T.J.3
  • 31
    • 0030272778 scopus 로고    scopus 로고
    • The use of 3-methoxymethyl-16β,17β-epiestriol-O-cyclic sulfone as the precursor in the synthesis of F-18 16α-fluoroestradiol
    • Lim J.L., Zheng L., Berridge M.S., Tewson T.J. The use of 3-methoxymethyl-16β, 17β-epiestriol-O-cyclic sulfone as the precursor in the synthesis of F-18 16α-fluoroestradiol. Nucl Med Biol. 23:1996;911-915
    • (1996) Nucl Med Biol , vol.23 , pp. 911-915
    • Lim, J.L.1    Zheng, L.2    Berridge, M.S.3    Tewson, T.J.4
  • 32
    • 0036026463 scopus 로고    scopus 로고
    • Synthesis of 16α-fluoro ICI 182,780 derivatives: Powerful antiestrogens to image estrogen receptor densities in breast cancer by positron emission tomography
    • Seimbille Y., Bénard F., van Lier J.E. Synthesis of 16α-fluoro ICI 182, 780 derivatives Powerful antiestrogens to image estrogen receptor densities in breast cancer by positron emission tomography. J Chem Soc Perkin Trans 1. 20:2000;2275-2281
    • (2000) J Chem Soc Perkin Trans 1 , vol.20 , pp. 2275-2281
    • Seimbille, Y.1    Bénard, F.2    Van Lier, J.E.3
  • 35
    • 0025280171 scopus 로고
    • Cyclic sulfates: Useful substrates for selective nucleophilic substitution
    • Berridge M.S., Franceschini M.P., Rosenfeld E., Tewson T.J. Cyclic sulfates Useful substrates for selective nucleophilic substitution. J Org Chem. 55:1990;1211-1217
    • (1990) J Org Chem , vol.55 , pp. 1211-1217
    • Berridge, M.S.1    Franceschini, M.P.2    Rosenfeld, E.3    Tewson, T.J.4
  • 37
    • 0025785380 scopus 로고
    • Synthesis and biological activity of new halo-steroidal antiestrogens
    • Levesque C., Merand Y., Dufour J.-M., Labrie C., Labrie F. Synthesis and biological activity of new halo-steroidal antiestrogens. J Med Chem. 34:1991;1624-1630
    • (1991) J Med Chem , vol.34 , pp. 1624-1630
    • Levesque, C.1    Merand, Y.2    Dufour, J.-M.3    Labrie, C.4    Labrie, F.5
  • 38
    • 0029089266 scopus 로고
    • The pure antiestrogen ICI 182,780 binds to a high-affinity site distinct from the estrogen receptor
    • Parisot J.P., Hu X.F., Sutherland R.L., Wakeling W., Zalcberg J.R., DeLuise M. The pure antiestrogen ICI 182, 780 binds to a high-affinity site distinct from the estrogen receptor. Int J Cancer. 62:1995;480-484
    • (1995) Int J Cancer , vol.62 , pp. 480-484
    • Parisot, J.P.1    Hu, X.F.2    Sutherland, R.L.3    Wakeling, W.4    Zalcberg, J.R.5    Deluise, M.6
  • 39
    • 0034724293 scopus 로고    scopus 로고
    • Activation of the human estrogen receptor by the antiestrogen ICI 182,780 and tamoxifen in yeast genetic systems: Implications for their mechanism of action
    • Dudley M.W., Sheeler C.Q., Wang H., Khan S. Activation of the human estrogen receptor by the antiestrogen ICI 182, 780 and tamoxifen in yeast genetic systems Implications for their mechanism of action. Proc Natl Acad Sci USA. 97:2000;3696-3701
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 3696-3701
    • Dudley, M.W.1    Sheeler, C.Q.2    Wang, H.3    Khan, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.