| Literature DB >> 33087320 |
Kartika Venugopal1, Yang Feng1, Daniil Shabashvili1, Olga A Guryanova2,3.
Abstract
In the last decade, large-scale genomic studies in patients with hematologic malignancies identified recurrent somatic alterations in epigenetic modifier genes. Among these, the de novo DNA methyltransferase DNMT3A has emerged as one of the most frequently mutated genes in adult myeloid as well as lymphoid malignancies and in clonal hematopoiesis. In this review, we discuss recent advances in our understanding of the biochemical and structural consequences of DNMT3A mutations on DNA methylation catalysis and binding interactions and summarize their effects on epigenetic patterns and gene expression changes implicated in the pathogenesis of hematologic malignancies. We then review the role played by mutant DNMT3A in clonal hematopoiesis, accompanied by its effect on immune cell function and inflammatory responses. Finally, we discuss how this knowledge informs therapeutic approaches for hematologic malignancies with mutant DNMT3A. ©2020 American Association for Cancer Research.Entities:
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Year: 2020 PMID: 33087320 PMCID: PMC7855745 DOI: 10.1158/0008-5472.CAN-20-3033
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 13.312