Fig. 1.
The overview of epigenetic regulation of hematologic malignancies. Epigenetic regulation of hematologic malignancies mainly includes DNA methylation, histone acetylation, histone methylation, and noncoding RNA. First, DNA methylation depends on writers, readers, and erasers. DNMTs are writers of DNA methylation, and targeted treatments focusing on DNMTs have been developed. Readers of DNA methylation include MBD-containing proteins, methyl-CpG binding zinc fingers, and SRA domain-containing proteins. Erasers of DNA methylation mainly consist of the TET family and the AID/APOBEC family. Second, histone acetylation depends on the writer KATs, the reader acetyl-lysine binding proteins, and the eraser HDACs. Correspondingly, innovative treatments targeting KATs, BETs, and HDACs are being developed. Third, histone methylation depends on the writer KMTs, the reader methyl-histone binding proteins, and the eraser KDMs. KMT inhibitors and KDM inhibitors are being explored in the treatment of hematologic malignancies. In addition, microRNAs and long noncoding RNAs also contribute to hematologic oncogenesis