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10.1038/bcj.2015.89

http://scihub22266oqcxt.onion/10.1038/bcj.2015.89
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suck abstract from ncbi


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pmid26473533
      Blood+Cancer+J 2015 ; 5 (10 ): e361
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  • Mutation of chromatin modifiers; an emerging hallmark of germinal center B-cell lymphomas #MMPMID26473533
  • Lunning MA ; Green MR
  • Blood Cancer J 2015[Oct]; 5 (10 ): e361 PMID26473533 show ga
  • Subtypes of non-Hodgkin's lymphomas align with different stages of B-cell development. Germinal center B-cell (GCB)-like diffuse large B-cell lymphoma (DLBCL), follicular lymphoma (FL) and Burkitt's lymphoma (BL) each share molecular similarities with normal GCB cells. Recent next-generation sequencing studies have gained insight into the genetic etiology of these malignancies and revealed a high frequency of mutations within genes encoding proteins that modifying chromatin. These include activating and inactivating mutations of genes that perform post-translational modification of histones and organize chromatin structure. Here, we discuss the function of histone acetyltransferases (CREBBP, EP300), histone methyltransferases (KDM2C/D, EZH2) and regulators of higher order chromatin structure (HIST1H1C/D/E, ARID1A and SMARCA4) that have been reported to be mutated in ?5% of DLBCL, FL or BL. Mutations of these genes are an emerging hallmark of lymphomas with GCB-cell origins, and likely represent the next generation of therapeutic targets for these malignancies.
  • |*Mutation [MESH]
  • |Animals [MESH]
  • |Chromatin [MESH]
  • |Germinal Center/pathology [MESH]
  • |Histone Acetyltransferases/*genetics [MESH]
  • |Histone Methyltransferases [MESH]
  • |Histone-Lysine N-Methyltransferase/*genetics [MESH]
  • |Humans [MESH]
  • |Lymphoma, Large B-Cell, Diffuse/*genetics [MESH]


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