Extensive Promoter DNA Hypermethylation and Hypomethylation Is Associated with Aberrant MicroRNA Expression in Chronic Lymphocytic Leukemia

Baer, Constance and , Rainer and Frenzel, Lukas P. and Zucknick, Manuela and Park, Yoon Jung and Gu, Lei and Weichenhan, Dieter and Fischer, Martina and Pallasch, Christian Philipp and Herpel, Esther and Rehli, Michael and Byrd, John C. and Wendtner, Clemens-Martin and Plass, Christoph (2012) Extensive Promoter DNA Hypermethylation and Hypomethylation Is Associated with Aberrant MicroRNA Expression in Chronic Lymphocytic Leukemia. CANCER RESEARCH, 72 (15). pp. 3775-3785. ISSN 0008-5472,

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Abstract

Dysregulated microRNA (miRNA) expression contributes to the pathogenesis of hematopoietic malignancies, including chronic lymphocytic leukemia (CLL). However, an understanding of the mechanisms that cause aberrant miRNA transcriptional control is lacking. In this study, we comprehensively investigated the role and extent of miRNA epigenetic regulation in CLL. Genome-wide profiling conducted on 24 CLL and 10 healthy B cell samples revealed global DNA methylation patterns upstream of miRNA sequences that distinguished malignant from healthy cells and identified putative miRNA promoters. Integration of DNA methylation and miRNA promoter data led to the identification of 128 recurrent miRNA targets for aberrant promoter DNA methylation. DNA hypomethylation accounted for more than 60% of all aberrant promoter-associated DNA methylation in CLL, and promoter DNA hypomethylation was restricted to well-defined regions. Individual hyper- and hypomethylated promoters allowed discrimination of CLL samples from healthy controls. Promoter DNA methylation patterns were confirmed in an independent patient cohort, with 11 miRNAs consistently showing an inverse correlation between DNA methylation status and expression level. Together, our findings characterize the role of epigenetic changes in the regulation of miRNA transcription and create a repository of disease-specific promoter regions that may provide additional insights into the pathogenesis of CLL. Cancer Res; 72(15); 3775-85. (C) 2012 AACR.

Item Type: Article
Uncontrolled Keywords: HUMAN CANCER-CELLS; EPIGENETIC REGULATION; DOWN-REGULATION; GENES; METHYLATION; GENOME; SIGNATURES; APOPTOSIS; LYMPHOMA; TARGETS;
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin III (Hämatologie und Internistische Onkologie)
Depositing User: Dr. Gernot Deinzer
Date Deposited: 07 May 2020 07:01
Last Modified: 07 May 2020 07:01
URI: https://pred.uni-regensburg.de/id/eprint/18371

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