Somatic Mutations Drive Specific, but Reversible, Epigenetic Heterogeneity States in AML.


Journal

Cancer discovery
ISSN: 2159-8290
Titre abrégé: Cancer Discov
Pays: United States
ID NLM: 101561693

Informations de publication

Date de publication:
12 2020
Historique:
received: 01 08 2019
revised: 09 07 2020
accepted: 11 09 2020
pubmed: 18 9 2020
medline: 25 11 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

Epigenetic allele diversity is linked to inferior prognosis in acute myeloid leukemia (AML). However, the source of epiallele heterogeneity in AML is unknown. Herein we analyzed epiallele diversity in a genetically and clinically annotated AML cohort. Notably, AML driver mutations linked to transcription factors and favorable outcome are associated with epigenetic destabilization in a defined set of susceptible loci. In contrast, AML subtypes linked to inferior prognosis manifest greater abundance and highly stochastic epiallele patterning. We report an epiallele outcome classifier supporting the link between epigenetic diversity and treatment failure. Mouse models with

Identifiants

pubmed: 32938585
pii: 2159-8290.CD-19-0897
doi: 10.1158/2159-8290.CD-19-0897
pmc: PMC7710625
mid: NIHMS1630381
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1934-1949

Subventions

Organisme : NCI NIH HHS
ID : R01 CA198089
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA034196
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM133562
Pays : United States
Organisme : NCI NIH HHS
ID : K08 CA181507
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA233332
Pays : United States

Informations de copyright

©2020 American Association for Cancer Research.

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Auteurs

Sheng Li (S)

The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut. amm2014@med.cornell.edu sheng.li@jax.org.
The Jackson Laboratory Cancer Center, Bar Harbor, Maine.
The Department of Genetics and Genomic Sciences, The University of Connecticut Health Center, Farmington, Connecticut.
Department of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut.

Xiaowen Chen (X)

The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.

Jiahui Wang (J)

The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut.

Cem Meydan (C)

Department of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.

Jacob L Glass (JL)

Leukemia Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

Alan H Shih (AH)

Center for Hematologic Malignancies, Memorial Sloan Kettering Cancer Center, New York, New York.

Ruud Delwel (R)

Department of Hematology, Erasmus University Medical Center and Oncode Institute, Rotterdam, the Netherlands.

Ross L Levine (RL)

Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.

Christopher E Mason (CE)

Department of Physiology and Biophysics, Weill Cornell Medicine, New York, New York.

Ari M Melnick (AM)

Division of Hematology/Oncology, Weill Cornell Medicine, New York, New York. amm2014@med.cornell.edu sheng.li@jax.org.

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Classifications MeSH