| Literature DB >> 28987382 |
Baolai Zhang1, Su Zhang2, Lijuan Zhu3, Xue Chen2, Yunfeng Zhao2, Li Chao2, Juanping Zhou2, Xing Wang2, Xinyang Zhang2, Nengqian Ma2.
Abstract
Arginine methylation is carried out by protein arginine methyltransferase (PRMTs) family. Arginine methyltransferase inhibitor 1 (AMI-1) is mainly used to inhibit type I PRMT activity in vitro. However, the effects of AMI-1 on type II PRMT5 activity and gastric cancer (GC) remain unclear. In this study, we provided the first evidence that AMI-1 significantly inhibited GC cell proliferation and migration while induced GC cell apoptosis, and reduced the expression of PRMT5, eukaryotic translation initiation factor 4E (eIF4E), symmetric dimethylation of histone 3 (H3R8me2s) and histone 4 (H4R3me2s). In addition, AMI-1 inhibited tumor growth, downregulated eIF4E, H4R3me2s and H3R8me2s expression in mice xenografts model of GC. Collectively, our results suggest that AMI-1 inhibits GC by downregulating eIF4E and targeting type II PRMT5.Entities:
Keywords: Arginine methyltransferase inhibitor 1 (AMI-1); Gastric cancer; Histonemethylation; Protein arginine methyltransferase 5 (PRMT5); eIF4E
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Year: 2017 PMID: 28987382 DOI: 10.1016/j.taap.2017.10.002
Source DB: PubMed Journal: Toxicol Appl Pharmacol ISSN: 0041-008X Impact factor: 4.219