4.8 Article

Chromatin Accessibility Landscape of Cutaneous T Cell Lymphoma and Dynamic Response to HDAC Inhibitors

Journal

CANCER CELL
Volume 32, Issue 1, Pages 27-+

Publisher

CELL PRESS
DOI: 10.1016/j.ccell.2017.05.008

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Funding

  1. Haas Family Foundation
  2. NIH [P50-HG007735, R35-CA209919]
  3. Stanford Cancer Institute
  4. National Natural Science Foundation of China [91640113]
  5. Chinese Government 1000 Youth Talent Program
  6. University of Science and Technology of China

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Here, we define the landscape and dynamics of active regulatory DNA in cutaneous T cell lymphoma (CTCL) by ATAC-seq. Analysis of 111 human CTCL and control samples revealed extensive chromatin signatures that distinguished leukemic, host, and normal CD4(+)T cells. We identify three dominant patterns of transcription factor (TF) activation that drive leukemia regulomes, as well as TF deactivations that alter host T cells in CTCL patients. Clinical response to histone deacetylase inhibitors (HDACi) is strongly associated with a concurrent gain in chromatin accessibility. HDACi causes distinct chromatin responses in leukemic and host CD4(+)T cells, reprogramming host T cells toward normalcy. These results provide a foundational framework to study personal regulomes in human cancer and epigenetic therapy.

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