Insights for the design of protein lysine methyltransferase G9a inhibitors

Author:

Charles Mariasoosai Ramya Chandar1,Dhayalan Arunkumar2,Hsieh Hsing-Pang3,Coumar Mohane Selvaraj1

Affiliation:

1. Centre for Bioinformatics, Pondicherry University, Kalapet, Puducherry 605014, India

2. Department of Biotechnology, Pondicherry University, Kalapet, Puducherry 605 014, India

3. Institute of Biotechnology & Pharmaceutical Research, National Health Research Institutes, 35 Keyan Road, Zhunan, Miaoli County 350, ROC Taiwan

Abstract

The epigenetic control of gene expression could be affected by addition and/or removal of post-translational modifications such as phosphorylation, acetylation and methylation of histone proteins, as well as methylation of DNA (5-methylation on cytosines). Misregulation of these modifications is associated with altered gene expression, resulting in various disease conditions. G9a belongs to the protein lysine methyltransferases that specifically methylates the K9 residue of histone H3, leading to suppression of several tumor suppressor genes. In this review, G9a functions, role in various diseases, structural biology aspects for inhibitor design, structure–activity relationship among the reported inhibitors are discussed which could aid in the design and development of potent G9a inhibitors for cancer treatment in the future.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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