Mechanisms of aromatase inhibitor resistance

被引:289
|
作者
Ma, Cynthia X. [1 ]
Reinert, Tomas [2 ]
Chmielewska, Izabela [3 ]
Ellis, Matthew J. [4 ]
机构
[1] Washington Univ, Sch Med, Dept Med, Siteman Canc Ctr,Div Oncol, St Louis, MO 63110 USA
[2] Inst Nacl Canc INCA, Dept Med Oncol, BR-20230130 Rio De Janeiro, Brazil
[3] Med Univ Lublin, Dept Pneumonol Oncol & Allergol, PL-20954 Lublin, Poland
[4] Baylor Coll Med, Lester & Sue Smith Breast Ctr, Houston, TX 77030 USA
关键词
ESTROGEN-RECEPTOR-ALPHA; BREAST-CANCER CELLS; GROWTH-FACTOR RECEPTOR; HISTONE DEACETYLASE INHIBITOR; RANDOMIZED PHASE-II; REGULATORY T-CELLS; ENDOCRINE THERAPY RESPONSIVENESS; ESR1 GENE AMPLIFICATION; POSITIVE HR PLUS; TAMOXIFEN RESISTANCE;
D O I
10.1038/nrc3920
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oestrogen receptor-positive (ER+) breast cancer is a major cause of cancer death in women. Although aromatase inhibitors suppress the function of ER and reduce the risk of recurrence, therapeutic resistance is common and essentially inevitable in advanced disease. This Review considers both genomic and cell biological explanations as to why ER+ breast cancer cells persist, progress and cause an incurable, lethal, systemic disease. The design and outcomes of clinical trials are considered with the perspective that resistance mechanisms are heterogeneous, and therefore biomarker and somatic mutation-based stratification and eligibility will be essential for improvements in patient outcomes.
引用
收藏
页码:261 / 275
页数:15
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