1. Therapeutic potential of enhancer of zeste homolog 2 in autoimmune diseases
- Author
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Hai-Feng Pan, Napoleon Bellua Sam, Liang-Yu Xie, Fan Cao, Guang-Lin Zhu, De-Guang Wang, Yue-Xin Yang, and Hui-Hui Shen
- Subjects
0301 basic medicine ,Clinical Biochemistry ,Bioinformatics ,Inflammatory bowel disease ,Autoimmune Diseases ,Epigenesis, Genetic ,03 medical and health sciences ,0302 clinical medicine ,Drug Development ,Drug Discovery ,medicine ,Animals ,Humans ,Enhancer of Zeste Homolog 2 Protein ,Epigenetics ,skin and connective tissue diseases ,Pharmacology ,Autoimmune disease ,Type 1 diabetes ,business.industry ,Multiple sclerosis ,EZH2 ,medicine.disease ,030104 developmental biology ,030220 oncology & carcinogenesis ,Rheumatoid arthritis ,Etiology ,Molecular Medicine ,business - Abstract
Introduction: Autoimmune diseases (ADs) are idiopathic and heterogeneous disorders with contentious pathophysiology. Great strides have been made in epigenetics and its involvement in ADs. Zeste homolog 2 (EZH2) has sparked extensive interest because of its pleiotropic roles in distinct pathologic contexts.Areas covered: This review summarizes the epigenetic functions and the biological significance of EZH2 in the etiology of rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), type 1 diabetes (T1D), inflammatory bowel disease (IBD), multiple sclerosis (MS), and systemic sclerosis (SSc). A brief recapitulation of the therapeutic potential of EZH2 targeting is provided.Expert opinion: There are questions marks and controversies surrounding the feasibility and safety of EZH2 targeting; it is recommended in RA and SLE, but queried in T1D, IBD, MS, and SSc. Future work should focus on contrast studies, systematic analyses and preclinical studies with optimizing methodologies. Selective research studies conducted in a stage-dependent manner are necessary because of the relapsing-remitting clinical paradigms.
- Published
- 2019