4.5 Article

Switching under selection: how CoREST controls endocrine therapy resistance in ER+ breast cancer

Journal

NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 29, Issue 11, Pages 1040-1042

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41594-022-00858-9

Keywords

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Funding

  1. US National Institutes of Health [5T32GM133351, R01 CA228211]
  2. Pew-Stewart Scholars for Cancer Research
  3. American Cancer Society Research Scholar Award

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Recent research reveals that the CoREST complex plays a crucial role in regulating the acquisition of endocrine therapy resistance in estrogen receptor-positive breast cancers. Profiling data demonstrate that this resistance transition is associated with the functional retargeting of CoREST on chromatin, which occurs in coordination with cJUN and SWI/SNF (cBAF).
New research shows that the CoREST complex controls the acquisition of endocrine therapy resistance in estrogen receptor-positive breast cancers. Profiling data show that this resistance transition is accompanied by a functional retargeting of CoREST on chromatin in coordination with cJUN and SWI/SNF (cBAF).

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