Computer-aided screening for suppressor of variegation 4-20 homolog 1 inhibitors and their preliminary activity validation in human osteosarcoma. Issue 2 (22nd January 2021)

• Record Type: Journal Article
• Authors: Zheng, Ruxiao; Liang, Danfeng; Jiang, Na; Zhou, Jing; Long, Xin; Wang, Xin; Wu, Miaomiao; Wu, Chuangfang; Bao, Jinku
• Is Part Of: Journal of biomolecular structure & dynamics. Volume 39:Issue 2(2021)
• Page Start: 526
• Page End: 537
• Publication Date: 2021-01-22
• Subjects: SUV420H1 -- histone lysine methyltransferases -- H4K20me2 -- molecular docking -- molecular dynamics simulation -- virtual screening; Biomolecules -- Periodicals; Molecular structure -- Periodicals; Molecular Biology -- Periodicals; Biomechanics -- Periodicals; 572
• DOI: 10.1080/07391102.2019.1711187
• Languages: English
• ISSNs: 0739-1102

Abstract

Abstract: Histone methylation/demethylation facilitate to maintain balanced histone methylation levels and underpin gene regulation, playing the key roles in epigenetic regulation. Suppressor of variegation 4-20 homolog 1 (SUV420H1), a member of class Histone Lysine Methyltransferase and a key enzyme in the epigenetic regulation of the pathways controlling metabolism and tumorigenesis, is crucial to maintain cell homeostasis. The inhibition of SUV420H1 has emerged as a promising candidate for drug development and cancer therapy. Herein, two potential and potent SUV420H1 inhibitors (ZINC08398384, ZINC08439608) were identified through in silico approach and in vitro biological experiments. In vitro biological tests demonstrated that these compounds can inhibit the proliferation of U2OS cells and restrict its migration ability. And the level of dimethylation of lysine 20 on histone H4 (H4K20me2) was markedly decreased by these compounds-treatment in a dose-dependent manner. These results indicated that ZINC08398384 and ZINC08439608 are potential SUV420H1 inhibitors and could be developed as promising drug candidates applied to cancer epigenetic therapy. Communicated by Ramaswamy H. Sarma