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Chromatin Accessibility Landscape of Cutaneous T Cell Lymphoma and Dynamic Response to HDAC Inhibitors.
Qu, Kun; Zaba, Lisa C; Satpathy, Ansuman T; Giresi, Paul G; Li, Rui; Jin, Yonghao; Armstrong, Randall; Jin, Chen; Schmitt, Nathalie; Rahbar, Ziba; Ueno, Hideki; Greenleaf, William J; Kim, Youn H; Chang, Howard Y.
Afiliación
  • Qu K; CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences and Medical Center, University of Science and Technology of China, Hefei 230027, China; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269
  • Zaba LC; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, USA; Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Satpathy AT; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, USA; Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Giresi PG; Epinomics, Menlo Park, CA 94035, USA.
  • Li R; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, USA.
  • Jin Y; CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences and Medical Center, University of Science and Technology of China, Hefei 230027, China.
  • Armstrong R; Stanford Blood and Marrow Transplantation Cellular Therapy Facility, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Jin C; CAS Key Laboratory of Innate Immunity and Chronic Diseases, School of Life Sciences and Medical Center, University of Science and Technology of China, Hefei 230027, China.
  • Schmitt N; CNRSUMR 5164, Université de Bordeaux, Bordeaux 33076, France.
  • Rahbar Z; Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Ueno H; Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
  • Greenleaf WJ; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, USA; Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
  • Kim YH; Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: younkim@stanford.edu.
  • Chang HY; Center for Personal Dynamic Regulomes and Program in Epithelial Biology, Stanford University School of Medicine, CCSR 2155c, 269 Campus Drive, Stanford, CA 94305-5168, USA; Department of Dermatology, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: howchang@stanfo
Cancer Cell ; 32(1): 27-41.e4, 2017 07 10.
Article en En | MEDLINE | ID: mdl-28625481
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromatina / Regulación Neoplásica de la Expresión Génica / Linfoma Cutáneo de Células T / Inhibidores de Histona Desacetilasas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Cell Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromatina / Regulación Neoplásica de la Expresión Génica / Linfoma Cutáneo de Células T / Inhibidores de Histona Desacetilasas Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Cell Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article