Abstract:
:The largest subtype of breast cancer is characterized by the expression and activity of the estrogen receptor alpha (ERalpha/ER). Although several effective therapies have significantly improved survival, the adaptability of cancer cells means that patients frequently stop responding or develop resistance to endocrine treatment. ER does not function in isolation and multiple associating factors have been reported to play a role in regulating the estrogen-driven transcriptional program. This review focuses on the dynamic interplay between some of these factors which co-occupy ER-bound regulatory elements, their contribution to estrogen signaling, and their possible therapeutic applications. Furthermore, the review illustrates how some ER association partners can influence and reprogram the genomic distribution of the estrogen receptor. As this dynamic ER activity enables cancer cell adaptability and impacts the clinical outcome, defining how this plasticity is determined is fundamental to our understanding of the mechanisms of disease progression.
journal_name
Endocrinologyjournal_title
Endocrinologyauthors
Farcas AM,Nagarajan S,Cosulich S,Carroll JSdoi
10.1210/endocr/bqaa224subject
Has Abstractpub_date
2021-02-01 00:00:00issue
2eissn
0013-7227issn
1945-7170pii
6025411journal_volume
162pub_type
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