| Literature DB >> 28106467 |
Koorosh Korfi1, Sara Ali1, James A Heward1, Jude Fitzgibbon1.
Abstract
While follicular lymphoma (FL) is exquisitely responsive to immuno-chemotherapy, many patients follow a relapsing remitting clinical course driven in part by a common precursor cell (CPC) population. Advances in next generation sequencing have provided valuable insights into the genetic landscape of FL and its clonal evolution in response to therapy, implicating perturbations of epigenetic regulators as a hallmark of the disease. Recurrent mutations of histone modifiers KMT2D, CREBBP, EP300, EZH2, ARIDIA, and linker histones are likely early events arising in the CPC pool, rendering epigenetic based therapies conceptually attractive for treatment of indolent and transformed FL. This review provides a synopsis of the main epigenetic aberrations and the current efforts in development and testing of epigenetic therapies in this B cell malignancy.Entities:
Keywords: EZH2 inhibitors; Epigenetic mutations; HDAC inhibitors; epigenetic therapies; follicular lymphoma
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Year: 2017 PMID: 28106467 PMCID: PMC5453190 DOI: 10.1080/15592294.2017.1282587
Source DB: PubMed Journal: Epigenetics ISSN: 1559-2294 Impact factor: 4.528