4.8 Article

Enhancer Architecture and Essential Core Regulatory Circuitry of Chronic Lymphocytic Leukemia

期刊

CANCER CELL
卷 34, 期 6, 页码 982-+

出版社

CELL PRESS
DOI: 10.1016/j.ccell.2018.11.001

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资金

  1. NIH [PO1CA81534, R01CA213442-01A1]
  2. Leukemia and Lymphoma Society
  3. NCI Pathway to Independence Award [K99/R00CA190861]
  4. NSF [2011125001]
  5. American Cancer Society [130965-PF-17-036-01-DMC]
  6. Ashford Foundation
  7. NCI [R01CA193910]
  8. NIGMS [R01GM107427]
  9. Leukemia Lymphoma Society
  10. American Cancer Society
  11. Melton Family Fund
  12. Susan and Gary Rosenbach Fund
  13. Broad Institute

向作者/读者索取更多资源

Enhancer profiling is a powerful approach for discovering cis-regulatory elements that define the core transcriptional regulatory circuits of normal and malignant cells. Gene control through enhancer activity is often dominated by a subset of lineage-specific transcription factors. By integrating measures of chromatin accessibility and enrichment for H3K27 acetylation, we have generated regulatory landscapes of chronic lymphocytic leukemia (CLL) samples and representative cell lines. With super enhancer-based modeling of regulatory circuits and assessments of transcription factor dependencies, we discover that the essential super enhancer factor PAX5 dominates CLL regulatory nodes and is essential for CLL cell survival. Targeting enhancer signaling via BET bromodomain inhibition disrupts super enhancer-dependent gene expression with selective effects on CLL core regulatory circuitry, conferring potent anti-tumor activity.

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