MyoD1 promotes the transcription of BIK and plays an apoptosis-promoting role in the development of gastric cancer.

Abstract

Myogenic differentiation (MyoD) 1, which is known as a pivotal transcription factor during myogenesis, has been proven dysregulated in several cancers. However, litter is known about the precise role and downstream genes of MyoD1 in gastric cancer (GC) cells. Here, we report that MyoD1 is lowly expressed in primary GC tissues and cells. In our experiments, overexpression of MyoD1 inhibited cell proliferation. Downstream genes of MyoD1 regulation were investigated using RNA-Seq. As a result, 138 up-regulated genes and 20 down-regulated genes and 27 up-regulated lncRNAs and 20 down-regulated lncRNAs were identified in MyoD1 overexpressed MKN-45 cells, which participated in epithelial cell signaling in Helicobacter pylori infection, glycosaminoglycan biosynthesis (keratan sulfate), notch signaling pathway, and others. Among these genes, BIK was directly regulated by MyoD1 in GC cells and inhibited cancer cell proliferation. The BIK knockdown rescued the effects of MyoD1 overexpression on GC cells. In conclusion, MyoD1 inhibited cell proliferation via 158 genes and 47 lncRNAs downstream directly or indirectly that participated in multiple signaling pathways in GC, and among these, MyoD1 promotes BIK transcription by binding to its promoter, then promotes BIK-Bcl2-caspase 3 axis and regulates GC cell apoptosis.

• Authors: Fei Wu, Jinyuan Zhang, Qiuyu Jiang, Qian Li, Fang Li, Jia Li, Wei Lv, Xiaofei Wang, Yannan Qin, Chen Huang, Shuqun Zhang
• Journal: Cell cycle (Georgetown, Tex.) (Cell Cycle) Pg. 1-15 (May 03 2024) ISSN: 1551-4005 [Electronic] United States
• PMID: 38701194 (Publication Type: Journal Article)