Distinct Roles for BET Family Members in Estrogen Receptor ? Enhancer Function and Gene Regulation in Breast Cancer Cells.

ABSTRACT: The bromodomain family member proteins (BRD; BET proteins) are key coregulators for estrogen receptor alpha (ER?)-mediated transcriptional enhancers. The use of BRD-selective inhibitors has gained much attention as a potential treatment for various solid tumors, including ER-positive breast cancers. However, the roles of individual BET family members have largely remained unexplored. Here, we describe the role of BRDs in estrogen (E2)-dependent gene expression in ER?-positive breast cancer cells. We observed that chemical inhibition of BET family proteins with JQ1 impairs E2-regulated gene expression and growth in breast cancer cells. In addition, RNAi-mediated depletion of each BET family member (BRDs 2, 3, and 4) revealed partially redundant roles at ER? enhancers and for target gene transcription. Furthermore, we found a unique role of BRD3 as a molecular sensor of total BET family protein levels and activity through compensatory control of its own protein levels. Finally, we observed that BRD3 is recruited to a subset of ER?-binding sites (ERBS) that are enriched for active enhancer features, located in clusters of ERBSs likely functioning as "super enhancers," and associated with highly E2-responsive genes. Collectively, our results illustrate a critical and specific role for BET family members in ER?-dependent gene transcription. IMPLICATIONS: BRD3 is recruited to and controls the activity of a subset ER? transcriptional enhancers, providing a therapeutic opportunity to target BRD3 with BET inhibitors in ER?-positive breast cancers.

SUBMITTER: Murakami S 

PROVIDER: S-EPMC6891197 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature