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Volumn 69, Issue 11, 2009, Pages 4716-4723

The vascular endothelial growth factor receptor inhibitor PTK787/ZK222584 inhibits aromatase

Author keywords

[No Author keywords available]

Indexed keywords

ANDROSTENEDIONE; AROMATASE; ESTRADIOL; ESTROGEN RECEPTOR; VASCULOTROPIN RECEPTOR; VATALANIB;

EID: 66349084100     PISSN: 00085472     EISSN: 15387445     Source Type: Journal    
DOI: 10.1158/0008-5472.CAN-08-4711     Document Type: Article
Times cited : (24)

References (27)
  • 1
    • 0038210242 scopus 로고    scopus 로고
    • Aromatase inhibitors in breast cancer
    • DOI 10.1056/NEJMra023246
    • Smith IE, Dowsett M. Aromatase inhibitors in breast cancer. N Engl J Med 2003;348:2431-2442 (Pubitemid 36682823)
    • (2003) New England Journal of Medicine , vol.348 , Issue.24 , pp. 2431-2442
    • Smith, I.E.1    Dowsett, M.2
  • 3
    • 11444251764 scopus 로고    scopus 로고
    • Results of the ATAC (Arimidex, Tamoxifen, Alone or in Combination) trial after completion of 5 years' adjuvant treatment for breast cancer
    • DOI 10.1016/S0140-6736(04)17666-6, PII S0140673604176666
    • Howell A, Cuzick J, Baum M, et al. Results of the ATAC (Arimidex, Tamoxifen, Alone or in Combination) trial after completion of 5 years' adjuvant treatment for breast cancer. Lancet 2005;365:60-62 (Pubitemid 40082147)
    • (2005) Lancet , vol.365 , Issue.9453 , pp. 60-62
  • 7
    • 34548462626 scopus 로고    scopus 로고
    • Mechanisms of disease: Angiogenesis and the management of breast cancer
    • Banerjee S, Dowsett M, Ashworth A, Martin LA. Mechanisms of disease: angiogenesis and the management of breast cancer. Nat Clin Pract Oncol 2007;4:536-550
    • (2007) Nat Clin Pract Oncol , vol.4 , pp. 536-550
    • Banerjee, S.1    Dowsett, M.2    Ashworth, A.3    Martin, L.A.4
  • 8
    • 42049121934 scopus 로고    scopus 로고
    • Crosstalk between the estrogen receptor and the HER tyrosine kinase receptor family: Molecular mechanism and clinical implications for endocrine therapy resistance
    • Arpino G, Wiechmann L, Osborne CK, Schiff R. Crosstalk between the estrogen receptor and the HER tyrosine kinase receptor family: molecular mechanism and clinical implications for endocrine therapy resistance. Endocr Rev 2008;29:217-233
    • (2008) Endocr Rev , vol.29 , pp. 217-233
    • Arpino, G.1    Wiechmann, L.2    Osborne, C.K.3    Schiff, R.4
  • 9
    • 23044463773 scopus 로고    scopus 로고
    • Tumor-specific expression of vascular endothelial growth factor receptor 2 but not vascular endothelial growth factor or human epidermal growth factor receptor 2 is associated with impaired response to adjuvant tamoxifen in premenopausal breast cancer
    • DOI 10.1200/JCO.2005.08.126
    • Ryden L, Jirstrom K, Bendahl PO, et al. Tumor-specific expression of vascular endothelial growth factor receptor 2 but not vascular endothelial growth factor or human epidermal growth factor receptor 2 is associated with impaired response to adjuvant tamoxifen in premenopausal breast cancer. J Clin Oncol 2005;23:4695-4704 (Pubitemid 46224072)
    • (2005) Journal of Clinical Oncology , vol.23 , Issue.21 , pp. 4695-4704
    • Ryden, L.1    Jirstrom, K.2    Bendahl, P.-O.3    Ferno, M.4    Nordenskjold, B.5    Stal, O.6    Thorstenson, S.7    Jonsson, P.-E.8    Landberg, G.9
  • 12
    • 29144494969 scopus 로고    scopus 로고
    • The anti-oestrogen ICI 182,780, but not tamoxifen, inhibits the growth of MCF-7 breast cancer cells refractory to long-term oestrogen deprivation through down-regulation of oestrogen receptor and IGF signalling
    • DOI 10.1677/erc.1.00905
    • Martin LA, Pancholi S, Chan CM, et al. The anti-oestrogen ICI 182,780, but not tamoxifen, inhibits the growth of MCF-7 breast cancer cells refractory to long-term oestrogen deprivation through down-regulation of oestrogen receptor and IGF signalling. Endocr Relat Cancer 2005;12:1017-1036 (Pubitemid 41815794)
    • (2005) Endocrine-Related Cancer , vol.12 , Issue.4 , pp. 1017-1036
    • Martin, L.-A.1    Pancholi, S.2    Chan, C.M.W.3    Farmer, I.4    Kimberley, C.5    Dowsett, M.6    Johnston, S.R.D.7
  • 13
    • 0016293443 scopus 로고
    • Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione
    • Thompson EA, Jr., Siiteri PK. Utilization of oxygen and reduced nicotinamide adenine dinucleotide phosphate by human placental microsomes during aromatization of androstenedione. J Biol Chem 1974;249:5364-5372
    • (1974) J Biol Chem , vol.249 , pp. 5364-5372
    • Thompson Jr., E.A.1    Siiteri, P.K.2
  • 15
    • 0017184389 scopus 로고
    • A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
    • Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976;72:248-254
    • (1976) Anal Biochem , vol.72 , pp. 248-254
    • Bradford, M.M.1
  • 17
    • 0027167698 scopus 로고
    • Aromatase inhibitors: Synthesis, biological activity, and binding mode of azole-type compounds
    • DOI 10.1021/jm00062a012
    • Furet P, Batzl C, Bhatnagar A, Francotte E, Rihs G, Lang M. Aromatase inhibitors: synthesis, biological activity, and binding mode of azole-type compounds. J Med Chem 1993;36:1393-1400 (Pubitemid 23164496)
    • (1993) Journal of Medicinal Chemistry , vol.36 , Issue.10 , pp. 1393-1400
    • Furet, P.1    Batzl, C.2    Bhatnagar, A.3    Francotte, E.4    Rihs, G.5    Lang, M.6
  • 18
    • 33747402650 scopus 로고    scopus 로고
    • Two targets, one drug for new EGFR inhibitors
    • McNeil C. Two targets, one drug for new EGFR inhibitors. J Natl Cancer Inst 2006;98:1102-1103
    • (2006) J Natl Cancer Inst , vol.98 , pp. 1102-1103
    • McNeil, C.1
  • 20
    • 58149198589 scopus 로고    scopus 로고
    • A new therapeutic strategy against hormone-dependent breast cancer: The preclinical development of a dual aromatase and sulfatase inhibitor
    • Foster PA, Chander SK, Newman SP, et al. A new therapeutic strategy against hormone-dependent breast cancer: the preclinical development of a dual aromatase and sulfatase inhibitor. Clin Cancer Res 2008;14:6469-6477
    • (2008) Clin Cancer Res , vol.14 , pp. 6469-6477
    • Foster, P.A.1    Chander, S.K.2    Newman, S.P.3
  • 21
    • 38049018155 scopus 로고    scopus 로고
    • A quantitative analysis of kinase inhibitor selectivity
    • Karaman MW, Herrgard S, Treiber DK, et al. A quantitative analysis of kinase inhibitor selectivity. Nat Biotechnol 2008;26:127-132
    • (2008) Nat Biotechnol , vol.26 , pp. 127-132
    • Karaman, M.W.1    Herrgard, S.2    Treiber, D.K.3
  • 22
    • 58149339806 scopus 로고    scopus 로고
    • Structural basis for androgen specificity and oestrogen synthesis in human aromatase
    • Ghosh D, Griswold J, Erman M, Pangborn W. Structural basis for androgen specificity and oestrogen synthesis in human aromatase. Nature 2009;457:219-223
    • (2009) Nature , vol.457 , pp. 219-223
    • Ghosh, D.1    Griswold, J.2    Erman, M.3    Pangborn, W.4
  • 24
    • 34247849335 scopus 로고    scopus 로고
    • Target practice: Lessons from phase III trials with bevacizumab and vatalanib in the treatment of advanced colorectal cancer
    • DOI 10.1634/theoncologist.12-4-443
    • Los M, Roodhart JM, Voest EE. Target practice: lessons from phase III trials with bevacizumab and vatalanib in the treatment of advanced colorectal cancer. Oncologist 2007;12:443-450 (Pubitemid 46698722)
    • (2007) Oncologist , vol.12 , Issue.4 , pp. 443-450
    • Los, M.1    Roodhart, J.M.L.2    Voest, E.E.3
  • 25
    • 66349112122 scopus 로고    scopus 로고
    • Phase I study of the novel, oral angiogenesis inhibitor PTK787/ZK22584 (PTK/ZK): Evaluating the pharmacokinetic effect of a high-fat meal in pateints with hormone-refractory prostate cancer
    • George D OW, Gilligan T, Masson E, et al. Phase I study of the novel, oral angiogenesis inhibitor PTK787/ZK22584 (PTK/ZK): evaluating the pharmacokinetic effect of a high-fat meal in pateints with hormone-refractory prostate cancer. J Clin Oncol, ASCO Annual Meeting Proceedings 2004;22:4689.
    • (2004) J Clin Oncol, ASCO Annual Meeting Proceedings , vol.22 , pp. 4689
    • George, D.O.W.1    Gilligan, T.2    Masson, E.3
  • 26
    • 37849009384 scopus 로고    scopus 로고
    • Phase II, open-label study of PTK787/ZK222584 for the treatment of metastatic gastrointestinal stromal tumors resistant to imatinib mesylate
    • Joensuu H, De Braud F, Coco P, et al. Phase II, open-label study of PTK787/ZK222584 for the treatment of metastatic gastrointestinal stromal tumors resistant to imatinib mesylate. Ann Oncol 2008;19:173-177
    • (2008) Ann Oncol , vol.19 , pp. 173-177
    • Joensuu, H.1    De Braud, F.2    Coco, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.