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Therapeutic potential of enhancer of zeste homolog 2 in autoimmune diseases.
Yang, Yue-Xin; Shen, Hui-Hui; Cao, Fan; Xie, Liang-Yu; Zhu, Guang-Lin; Sam, Napoleon Bellua; Wang, De-Guang; Pan, Hai-Feng.
Affiliation
  • Yang YX; Department of Radiation Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
  • Shen HH; Department of Clinical Medicine, The second School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
  • Cao F; Department of Clinical Medicine, The second School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
  • Xie LY; Department of Clinical Medicine, The second School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
  • Zhu GL; Department of Clinical Medicine, The second School of Clinical Medicine, Anhui Medical University, Hefei, Anhui, China.
  • Sam NB; Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Anhui Province Key Laboratory of Major Autoimmune Diseases, Hefei, Anhui, China.
  • Wang DG; Department of Nephrology, The Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
  • Pan HF; Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Anhui Province Key Laboratory of Major Autoimmune Diseases, Hefei, Anhui, China.
Expert Opin Ther Targets ; 23(12): 1015-1030, 2019 12.
Article in En | MEDLINE | ID: mdl-31747802
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.
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Full text: 1 Database: MEDLINE Main subject: Autoimmune Diseases / Enhancer of Zeste Homolog 2 Protein / Drug Development Limits: Animals / Humans Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Autoimmune Diseases / Enhancer of Zeste Homolog 2 Protein / Drug Development Limits: Animals / Humans Language: En Year: 2019 Type: Article