标题:Helicobacter pylori CagA inhibits the expression of Runx3 via Src/MEK/ERK and p38 MAPK pathways in gastric epithelial cell
作者:Liu, Zhifang; Xu, Xia; Chen, Long; Li, Wenjuan; Sun, Yundong; Zeng, Jiping; Yu, Han; Chen, Chunyan; Jia, Jihui
作者机构:[Liu, Zhifang; Xu, Xia; Chen, Long; Li, Wenjuan; Sun, Yundong; Zeng, Jiping; Yu, Han; Chen, Chunyan; Jia, Jihui] Shandong Univ, Dept Biochem & Microbi 更多
通讯作者:Jia, JH
通讯作者地址:[Jia, JH]Shandong Univ, Dept Biochem & Microbiol, Key Lab Expt Teratol, Chinese Minist Educ,Sch Med, Jinan 250012, Peoples R China.
来源:JOURNAL OF CELLULAR BIOCHEMISTRY
出版年:2012
卷:113
期:3
页码:1080-1086
DOI:10.1002/jcb.23440
关键词:CagA; Runx3; REGULATION
摘要:Infection with CagA-positive Helicobacter pylori is the strongest risk factor for gastric carcinoma. Upon delivery into gastric epithelial cells, CagA disturbs cellular functions by physically interacting with and deregulating intracellular signaling molecules via both tyrosine phosphorylation-dependent and -independent mechanisms. Runx3 was suggested to be a tumor suppressor and closely associated with tumorigenesis and progression of gastric cancer. The aim of our study is to verify the effect of H. pylori virulence factor CagA on Runx3 expression level and investigate the corresponding molecular mechanisms and signaling pathways influencing Runx3 expression. Human gastric epithelial immortalized GES-1 cells were transfected with CagA-expression vector or control vector with FuGENE HD transfection reagent. Runx3 expression levels were determined by QRT-PCR and immunoblotting. Then we constructed a 1,150?bp Runx3 promoter luciferase reporter plasmid, pGL3-1150?bp, which was co-transfected into GES-1 cell with CagA-expression vector or control vector. Luciferase reporter assay was used to determine the effects of CagA on the 1,150?bp promoter activity of Runx3. Signal inhibitors were used to detect the signal pathway(s) through which CagA affects Runx3. Our results showed that CagA can reduce the expression level of Runx3 at both mRNA and protein levels significantly. Importantly, the 1,150?bp Runx3 promoter activity was decreased in cells transfected with CagA-expression vector comparing with cells transfected with control vector. And this inhibition is dependent on the phosphorylation of CagA. Signal pathways Src/MEK/ERK and p38 MAPK are involved in this regulation. Our findings provide new insights for understanding the mechanism of H. pylori carcinogenesis. J. Cell. Biochem. 113: 10801086, 2012. (C) 2011 Wiley Periodicals, Inc.
收录类别:SCOPUS;SCIE
WOS核心被引频次:24
Scopus被引频次:29
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863272507&doi=10.1002%2fjcb.23440&partnerID=40&md5=a9bdfb437c65f5c75bfbbb0959a6ab36
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