克洛丹
基质金属蛋白酶
紧密连接
癌症
细胞外基质
免疫组织化学
化学
癌症研究
生物
病理
细胞生物学
医学
生物化学
遗传学
作者
Li-Yu Lee,Chi-Ming Wu,Chee-Chan Wang,Jau-Song Yu,Ying Liang,Kuo-Hao Huang,Chih-Hong Lo,Tsann-Long Hwang
出处
期刊:Histology and Histopathology
[University of Murcia]
日期:2008-05-01
卷期号:23 (5): 515-21
被引量:18
摘要
Matrix metalloproteinases (MMPs) MMP-2 and MMP-9 can degrade type IV collagen of extracellular matrix and basal membranes. Claudin-4 is a member of a large family of transmembrane proteins, claudins, essential in the formation and maintenance of tight junctions. Claudin-4 has been shown to activate MMP-2, indicating that claudin-mediated increased cancer cell invasion might be mediated through the activation of MMP proteins. To explore the roles of MMP-2, MMP-9 and claudin-4 in gastric cancer, we selected 88 cases and then analyzed the expression of these proteins using immunohistochemistry. We found that all of MMP-2, MMP-9 and claudin-4 expressions were significantly higher in intestinal-type than in diffuse-type gastric cancer. On further analysis, testing the relationship between MMP-2 and MMP-9 expression with claudin-4 expression, claudin-4 expression was significantly associated with MMP-9 expression, but not with MMP-2 expression. The results showed that MMP-2, MMP-9 and claudin-4 expression may be phenotypic features, distinguishing intestinal-type and diffuse-type gastric cancer. Possibly, claudin-4 played a role in determining MMP-9 activity which favored intestinal-type gastric cancer to distal metastasis.
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