| Literature DB >> 20060365 |
Maria E Figueroa1, Sanne Lugthart, Yushan Li, Claudia Erpelinck-Verschueren, Xutao Deng, Paul J Christos, Elizabeth Schifano, James Booth, Wim van Putten, Lucy Skrabanek, Fabien Campagne, Madhu Mazumdar, John M Greally, Peter J M Valk, Bob Löwenberg, Ruud Delwel, Ari Melnick.
Abstract
We hypothesized that DNA methylation distributes into specific patterns in cancer cells, which reflect critical biological differences. We therefore examined the methylation profiles of 344 patients with acute myeloid leukemia (AML). Clustering of these patients by methylation data segregated patients into 16 groups. Five of these groups defined new AML subtypes that shared no other known feature. In addition, DNA methylation profiles segregated patients with CEBPA aberrations from other subtypes of leukemia, defined four epigenetically distinct forms of AML with NPM1 mutations, and showed that established AML1-ETO, CBFb-MYH11, and PML-RARA leukemia entities are associated with specific methylation profiles. We report a 15 gene methylation classifier predictive of overall survival in an independent patient cohort (p < 0.001, adjusted for known covariates). Copyright (c) 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20060365 PMCID: PMC3008568 DOI: 10.1016/j.ccr.2009.11.020
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743