Journal
FRONTIERS IN ENDOCRINOLOGY
Volume 14, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2023.1250218
Keywords
AIB1; SRC3; Ncoa3; estrogen receptor; breast cancer; endocrine therapy; transcriptional regulation
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Estrogen receptor alpha (ERα) plays a crucial role in the initiation and progression of most breast cancers. It regulates gene transcription through recruitment of coregulators, including Amplified in Breast Cancer 1 (AIB1). AIB1, an oncogene overexpressed in some breast cancers, is involved in tumor progression and resistance to endocrine therapy. This review provides an overview of the normal and pathological functions of AIB1, its actions dependent and independent of ERα, as well as its genomic conservation and protein evolution. The efforts to target AIB1 in the treatment of breast cancer are also discussed.
The estrogen receptor alpha (ER & alpha;) is a steroid receptor that is pivotal in the initiation and progression of most breast cancers. ER & alpha; regulates gene transcription through recruitment of essential coregulators, including the steroid receptor coactivator AIB1 (Amplified in Breast Cancer 1). AIB1 itself is an oncogene that is overexpressed in a subset of breast cancers and is known to play a role in tumor progression and resistance to endocrine therapy through multiple mechanisms. Here we review the normal and pathological functions of AIB1 in regard to its ER & alpha;-dependent and ER & alpha;-independent actions, as well as its genomic conservation and protein evolution. We also outline the efforts to target AIB1 in the treatment of breast cancer.
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