4.4 Review

G9a-An Appealing Antineoplastic Target

期刊

CURRENT CANCER DRUG TARGETS
卷 17, 期 6, 页码 555-568

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1568009616666160512145303

关键词

Histone Lysine Methltransferase; G9a; Biological functions; inhibitors; diseases; antineoplastic target

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资金

  1. National Natural Science Foundation of China [81230078, 81202463, 81502915, 81173087, 91129732]
  2. National Major Science and Technology Project of China (Innovation and Development of New Drugs) [2014ZX09507002-005-015, 2013ZX09402102-001-005, 2010ZX09401-401]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions

向作者/读者索取更多资源

Background: G9a is the primary enzyme for mono- and dimethylation at Lys 9 of histone H3 and forms predominantly the heteromeric complex as a G9a-GLP (G9a-like protein) that is a functional histone lysine methltransferase in vivo. Mounting evidence suggests that G9a catalyzes methylation of histone and nonhistone proteins, which plays a crucial role in diverse biological processes and human diseases. Methods: In this study, the current knowledge on biological functions of G9a and inhibitors were summarized. Results: we review the current knowledge on biological functions of G9a, with particular emphasis on regulating gene expression and cell processes, and involvement in human diseases. We outline a perspective on various classes of G9a inhibitors to date from both articles and patents with an emphasis on their discovery, activity and the current research status. Conclusion: We highlight the key knowledge on potential biological functions and various human diseases. We also reviewed the discovery and characterization of the reported G9a inhibitors. However, we also propose the challenges and future opportunities in study of G9a. This review could make a crucial contribution to the long journey to develop drug-like molecules targeting G9a.

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