Endocrine Resistance in Hormone Receptor Positive Breast Cancer-From Mechanism to Therapy

被引:150
作者
Rani, Aradhana [1 ]
Stebbing, Justin [2 ]
Giamas, Georgios [3 ]
Murphy, John [1 ]
机构
[1] Univ Westminster, Sch Life Sci, London, England
[2] Imperial Coll London, Dept Surg & Canc, London, England
[3] Univ Sussex, Dept Biochem & Biomed, Sch Life Sci, Brighton, E Sussex, England
来源
FRONTIERS IN ENDOCRINOLOGY | 2019年 / 10卷
关键词
endocrine resistance; breast cancer; signaling; estrogen (E2); estrogen receptor; GROWTH-FACTOR-RECEPTOR; NF-KAPPA-B; HUMAN ESTROGEN-RECEPTOR; SYK TYROSINE KINASE; ACQUIRED TAMOXIFEN RESISTANCE; HYPOXIA-INDUCIBLE FACTOR-1; ACTIVATING ESR1 MUTATIONS; GENOME-WIDE ASSOCIATION; RANDOMIZED PHASE-II; ER-ALPHA;
D O I
10.3389/fendo.2019.00245
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The importance and role of the estrogen receptor (ER) pathway has been well-documented in both breast cancer (BC) development and progression. The treatment of choice in women with metastatic breast cancer (MBC) is classically divided into a variety of endocrine therapies, 3 of the most common being: selective estrogen receptor modulators (SERM), aromatase inhibitors (AI) and selective estrogen receptor down-regulators (SERD). In a proportion of patients, resistance develops to endocrine therapy due to a sophisticated and at times redundant interference, at the molecular level between the ER and growth factor. The progression to endocrine resistance is considered to be a gradual, step-wise process. Several mechanisms have been proposed but thus far none of them can be defined as the complete explanation behind the phenomenon of endocrine resistance. Although multiple cellular, molecular and immune mechanisms have been and are being extensively studied, their individual roles are often poorly understood. In this review, we summarize current progress in our understanding of ER biology and the molecular mechanisms that predispose and determine endocrine resistance in breast cancer patients.
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页数:32
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