BMC Cancer | |
Protein arginine methyltransferase 5 regulates multiple signaling pathways to promote lung cancer cell proliferation | |
Research Article | |
Xiumei Sheng1  Zhengxin Wang2  | |
[1] School of Medicine, Jiangsu University, 2012013, Zhenjiang, Jiangsu Province, China;The Center for Cancer Research and Therapeutic Development, Department of Biological Sciences, Clark Atlanta University, 223 James P. Brawley Drive, S.W, 30314, Atlanta, GA, USA; | |
关键词: PRMT5; WDR77; p44; FGFR; ErbB; BTG2; GLIPR1; Lung cancer; | |
DOI : 10.1186/s12885-016-2632-3 | |
received in 2016-02-09, accepted in 2016-07-27, 发布年份 2016 | |
来源: Springer | |
【 摘 要 】
BackgroundProtein arginine methyltransferase 5 (PRMT5) catalyzes the formation of symmetrical dimethylation of arginine residues in proteins. WD repeat domain 77 (WDR77), also known as p44, MEP50, or WD45, forms a stoichiometric complex with PRMT5. The PRMT5/p44 complex is required for cellular proliferation of lung and prostate epithelial cells during earlier stages of development and is re-activated during prostate and lung tumorigenesis. The molecular mechanisms by which PRMT5 and p44 promote cellular proliferation are unknown.MethodsExpression of PRMT5 and p44 in lung and prostate cancer cells was silenced and their target genes were identified. The regulation of target genes was validated in various cancer cells during lung development and tumorigenesis. Altered expression of target genes was achieved by ectopic cDNA expression and shRNA-mediated silencing.ResultsPRMT5 and p44 regulate expression of a specific set of genes encoding growth and anti-growth factors, including receptor tyrosine kinases and antiproliferative proteins. Genes whose expression was suppressed by PRMT5 and p44 encoded anti-growth factors and inhibited cell growth when ectopically expressed. In contrast, genes whose expression was enhanced by PRMT5 and p44 encoded growth factors and increased cell growth when expressed. Altered expression of target genes is associated with re-activation of PRMT5 and p44 during lung tumorigenesis.ConclusionsOur data provide the molecular basis by which PRMT5 and p44 regulate cell growth and lay a foundation for further investigation of their role in lung tumor initiation.
【 授权许可】
CC BY
© The Author(s). 2016
【 预 览 】
Files | Size | Format | View |
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RO202311104695830ZK.pdf | 2152KB | download |
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