Post-translational modifications of EZH2 in cancer.
Zhongwei LiMinle LiDiandian WangPingfu HouXintian ChenSufang ChuDafei ChaiJun-Nian ZhengJin BaiPublished in: Cell & bioscience (2020)
Enhancer of zeste homolog 2 (EZH2), as a main component of Polycomb Repressive Complex 2, catalyzes histone H3K27me3 to silence its target gene expression. EZH2 upregulation results in cancer development and poor prognosis of cancer patients. Post-translational modifications (PTMs) are important biological events in cancer progression. PTMs regulate protein conformation and diversity functions. Recently, mounting studies have demonstrated that EZH2 stability, histone methyltransferase activity, localization, and binding partners can be regulated by PTMs, including phosphorylation, O-GlcNAcylation, acetylation, methylation and ubiquitination. However, the detailed molecular mechanisms of the EZH2-PTMs and whether other types of PTMs occur in EZH2 remain largely unclear. This review presents an overview of different roles of EZH2 modification and EZH2-PTMs crosstalk during tumorigenesis and cancer metastasis. We also discussed the therapeutic potential of targeting EZH2 modifications for cancer therapy.
Keyphrases
- long non coding rna
- poor prognosis
- papillary thyroid
- long noncoding rna
- gene expression
- cancer therapy
- dna methylation
- squamous cell
- cell proliferation
- squamous cell carcinoma
- lymph node metastasis
- drug delivery
- genome wide
- small molecule
- young adults
- men who have sex with men
- human immunodeficiency virus
- histone deacetylase