Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6156129 | Translational Research | 2015 | 36 Pages |
Abstract
Abnormal epigenetic patterning commonly is observed in cancer, including the myeloid malignancies acute myeloid leukemia and myelodysplastic syndromes. However, despite the universal nature of epigenetic deregulation, specific subtypes of myeloid disorders are associated with distinct epigenetic profiles, which accurately reflect the biologic heterogeneity of these disorders. In addition, mutations and genetic alterations of epigenetic-modifying enzymes frequently have been reported in these myeloid malignancies, emphasizing the importance of epigenetic deregulation in the initiation, progression, and outcome of these disorders. These aberrant epigenetic modifiers have become new targets for drug design, because their inhibition can potentially reverse the altered epigenetic landscapes that contribute to the development of the leukemia. In this review, we provide an overview of the role of epigenetic deregulation in leukemic transformation and their potential for therapeutic targeting.
Keywords
NPM15hmCMLLHOXA9EZH2AZAPRC2CMMLDNMT3AAzacytidineHSCDOT1LDNA methyltransferase 3aDNMTiMEIS1JmjCJumonji CASXL12-HGAMLDACIDH1HDACiIDH2TETα-KGSDHMPNHDACMBMMDS2-Hydroxyglutarate5mC5-Methylcytosine5-hydroxymethylcytosineDNA methyltransferase inhibitoralpha-ketoglutarateIsocitrate dehydrogenase 1isocitrate dehydrogenase 2Jarid2ten-eleven translocationDecitabineHematopoietic stem cellmyelodysplastic syndromesuccinate dehydrogenasefumarate hydrataseacute myeloid leukemiaMixed lineage leukemiachronic myelomonocytic leukemiahistone deacetylase inhibitorMyeloproliferative neoplasmnucleophosminhistone deacetylasepolycomb repressive complex 2
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Authors
Kristen M. Meldi, Maria E. Figueroa,