Unknown

Dataset Information

0

Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes.


ABSTRACT: Global investigation of histone marks in acute myeloid leukemia (AML) remains limited. Analyses of 38 AML samples through integrated transcriptional and chromatin mark analysis exposes 2 major subtypes. One subtype is dominated by patients with NPM1 mutations or MLL-fusion genes, shows activation of the regulatory pathways involving HOX-family genes as targets, and displays high self-renewal capacity and stemness. The second subtype is enriched for RUNX1 or spliceosome mutations, suggesting potential interplay between the 2 aberrations, and mainly depends on IRF family regulators. Cellular consequences in prognosis predict a relatively worse outcome for the first subtype. Our integrated profiling establishes a rich resource to probe AML subtypes on the basis of expression and chromatin data.

SUBMITTER: Yi G 

PROVIDER: S-EPMC6363099 | biostudies-literature | 2019 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications


Global investigation of histone marks in acute myeloid leukemia (AML) remains limited. Analyses of 38 AML samples through integrated transcriptional and chromatin mark analysis exposes 2 major subtypes. One subtype is dominated by patients with NPM1 mutations or MLL-fusion genes, shows activation of the regulatory pathways involving HOX-family genes as targets, and displays high self-renewal capacity and stemness. The second subtype is enriched for RUNX1 or spliceosome mutations, suggesting pote  ...[more]

Similar Datasets

| S-EPMC8579120 | biostudies-literature
| S-EPMC189079 | biostudies-other
| S-EPMC5396110 | biostudies-literature
| S-EPMC6784525 | biostudies-literature
| S-EPMC5812697 | biostudies-literature
2016-12-11 | GSE85499 | GEO
| S-EPMC8947610 | biostudies-literature
| S-EPMC4878860 | biostudies-literature
| S-EPMC5426990 | biostudies-literature
| S-EPMC7509144 | biostudies-literature