Aromatase inhibitors: Future directions

被引:23
作者
Osborne, CK
Schiff, R
机构
[1] Baylor Coll Med, Breast Ctr, Houston, TX 77030 USA
[2] Methodist Hosp, Houston, TX 77030 USA
关键词
D O I
10.1016/j.jsbmb.2005.04.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Estrogen and its cognate estrogen receptor are key players in the etiology and progression of breast cancer. Aromatase inhibitors, suppressing tumor and plasma estrogen levels by blocking testosterone conversion to estrogen, have been proven to provide the most effective endocrine therapy for postmenopausal breast cancer patients. Aromatase inhibitors are now the first choice endocrine therapy in the metastatic setting for postmenopausal women. These endocrine agents also seem likely to soon become the standard adjuvant therapy, either alone or in sequence with tamoxifen, though their long-term toxicity and the optimum duration of therapy still remain to be defined. Advanced experimental studies and some clinical observations reveal the importance of blocking both the genomic and non-genomic activities of the estrogen receptor, as well as its crosstalk with growth factor and other cellular signaling, for greatest effectiveness of endocrine therapy. Consequently, these studies provide a mechanistic explanation for the superb performance of aromatase inhibitors, and also suggest how inhibiting selected growth factor receptors might delay or prevent the onset of resistance to aromatase inhibitors and other endocrine therapies. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:183 / 187
页数:5
相关论文
共 32 条
  • [1] Arpino G, 2004, BREAST CANCER RES TR, V88, pS15
  • [2] Progesterone receptor status significantly improves outcome prediction over estrogen receptor status alone for adjuvant endocrine therapy in two large breast cancer databases
    Bardou, VJ
    Arpino, G
    Elledge, RM
    Osborne, CK
    Clark, GM
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (10) : 1973 - 1979
  • [3] Baum M, 2002, LANCET, V359, P2131
  • [4] Buzdar AU, 1998, CANCER-AM CANCER SOC, V83, P1142, DOI 10.1002/(SICI)1097-0142(19980915)83:6<1142::AID-CNCR13>3.3.CO
  • [5] 2-7
  • [6] Clarke M, 1998, LANCET, V351, P1451
  • [7] A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with primary breast cancer
    Coombes, RC
    Hall, E
    Gibson, LJ
    Paridaens, R
    Jassem, J
    Delozier, T
    Jones, SE
    Alvarez, I
    Bertelli, G
    Ortmann, O
    Coates, AS
    Bajetta, E
    Dodwell, D
    Coleman, RE
    Fallowfield, LJ
    Mickiewicz, E
    Andersen, J
    Lonning, PE
    Cocconi, G
    Stewart, A
    Stuart, N
    Snowdon, CF
    Carpentieri, M
    Massimini, G
    Bliss, JM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (11) : 1081 - 1092
  • [8] Insulin-like growth factor-I inhibits progesterone receptor expression in breast cancer cells via the phosphatidylinositol 3-kinase/akt/mammalian target of rapamycin pathway: Progesterone receptor as a potential indicator of growth factor activity in breast cancer
    Cui, XJ
    Zhang, P
    Deng, WL
    Oesterreich, S
    Lu, YL
    Mills, GB
    Lee, AV
    [J]. MOLECULAR ENDOCRINOLOGY, 2003, 17 (04) : 575 - 588
  • [9] Letrozole, a new oral aromatase inhibitor for advanced breast cancer: Double-blind randomized trial showing a dose effect and improved efficacy and tolerability compared with megestrol acetate
    Dombernowsky, P
    Smith, I
    Falkson, G
    Leonard, R
    Panasci, L
    Bellmunt, J
    Bezwoda, W
    Gardin, G
    Gudgeon, A
    Morgan, M
    Fornasiero, A
    Hoffmann, W
    Michel, J
    Hatschek, T
    Tjabbes, T
    Chaudri, HA
    Hornberger, U
    Trunet, PF
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) : 453 - 461
  • [10] Dowsett M, 2003, BREAST CANCER RES TR, V82, pS7