中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Increased Expression of Protease-Activated Receptor 4 and Trefoil Factor 2 in Human Colorectal Cancer

文献类型:期刊论文

作者Yu GY1,2; Jiang P1,3; Xiang Y[*]1; Zhang Y1; Zhu Z4; Zhang CR5; Lee S2; Lee WH1; Zhang Y[*]1
刊名PLOS ONE
出版日期2015
卷号10期号:4页码:e0122678
通讯作者yang_xiang000@hotmail.com ; zhangy@mail.kiz.ac.cn
合作状况其它
英文摘要Protease-activated receptor 4 (PAR4), a member of G-protein coupled receptors family, was recently reported to exhibit decreased expression in gastric cancer and esophageal squamous cancer, yet increased expression during the progression of prostate cancer. Trefoil factor 2 (TFF2), a small peptide constitutively expressed in the gastric mucosa, plays a protective role in restitution of gastric mucosa. Altered TFF2 expression was also related to the development of gastrointestinal cancer. TFF2 has been verified to promote cell migration via PAR4, but the roles of PAR4 and TFF2 in the progress of colorectal cancer are still unknown. In this study, the expression level of PAR4 and TFF2 in colorectal cancer tissues was measured using real-time PCR (n = 38), western blotting (n = 38) and tissue microarrays (n = 66). The mRNA and protein expression levels of PAR4 and TFF2 were remarkably increased in colorectal cancer compared with matched noncancerous tissues, especially in positive lymph node and poorly differentiated cancers. The colorectal carcinoma cell LoVo showed an increased response to TFF2 as assessed by cell invasion upon PAR4 expression. However, after intervention of PAR4 expression, PAR4 positive colorectal carcinoma cell HT-29 was less responsive to TFF2 in cell invasion. Genomic bisulfite sequencing showed the hypomethylation of PAR4 promoter in colorectal cancer tissues and the hypermethylation in the normal mucosa that suggested the low methylation of promoter was correlated to the increased PAR4 expression. Taken together, the results demonstrated that the up-regulated expression of PAR4 and TFF2 frequently occurs in colorectal cancer tissues, and that overexpression of PAR4 may be resulted from promoter hypomethylation. While TFF2 promotes invasion activity of LoVo cells overexpressing PAR4, and this effect was significantly decreased when PAR4 was knockdowned in HT-29 cells. Our findings will be helpful in further investigations into the functions and molecular mechanisms of Proteinase-activated receptors (PARs) and Trefoil factor factors (TFFs) during the progression of colorectal cancer.
资助信息This work was supported by grants from the Chinese National Natural Science Foundation (81160302, 31270835), the Chinese Academy of Sciences (KJZD-EW-L03), Yunnan Province Science and Technology Department BasicResearch Foundation (2011FZ109) and State Key Laboratory of Genetic Resource and Evolution (GREKF11-13).
收录类别SCI
语种英语
WOS记录号WOS:000352845100093
公开日期2015-06-08
源URL[http://159.226.149.42:8088/handle/152453/8342]  
专题昆明动物研究所_动物活性蛋白多肽组学
昆明动物研究所_动物模型与人类重大疾病机理重点实验室
作者单位1.Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan 650223, China
2.Department of Biochemistry, Kunming Medical University, Kunming, Yunnan 650500, China
3.Department of Pathology and Pathophysiology, Kunming Medical University, Kunming, Yunnan 650500, China
4.Department of Gastroenterology, the First Affiliated Hospital of Kunming Medical University, Kunming 650032, China
5.Department of Functional Experimental Center, Kunming Medical University, Kunming, Yunnan 650500, China
推荐引用方式
GB/T 7714
Yu GY,Jiang P,Xiang Y[*],et al. Increased Expression of Protease-Activated Receptor 4 and Trefoil Factor 2 in Human Colorectal Cancer[J]. PLOS ONE,2015,10(4):e0122678.
APA Yu GY.,Jiang P.,Xiang Y[*].,Zhang Y.,Zhu Z.,...&Zhang Y[*].(2015).Increased Expression of Protease-Activated Receptor 4 and Trefoil Factor 2 in Human Colorectal Cancer.PLOS ONE,10(4),e0122678.
MLA Yu GY,et al."Increased Expression of Protease-Activated Receptor 4 and Trefoil Factor 2 in Human Colorectal Cancer".PLOS ONE 10.4(2015):e0122678.

入库方式: OAI收割

来源:昆明动物研究所

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