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Investigation of the mechanisms of coagulation factor Ⅶa-induced colon cancer 8W620 cell proliferation and migration
引用本文:石文霞,周红,李娜,黄宏亮,周保成.Investigation of the mechanisms of coagulation factor Ⅶa-induced colon cancer 8W620 cell proliferation and migration[J].中华肿瘤杂志,2000,31(1):485-489.
作者姓名:石文霞  周红  李娜  黄宏亮  周保成
作者单位:江苏大学基础医学与医学技术学院,镇江,212013;
基金项目:教育部回国人员科研启动基金江苏大学学生科研立项基金
摘    要:Objective To investigate the mechanisms that coagulation factor Ⅶa promotes proliferation and migration of a colon cancer cell line (SW620 cells) in vitro. Methods The expression of interleukin 8 (IL-8), tissue factor (TF), caspase-7 and p-p38 MAPK in SW620 cells treated with factor Ⅶa or protease activated receptor 2 aganist (PAR2-AP) was measured by ELISA, Western-blotting and QT-PCR. Results Factor Ⅶa and PAR2-AP induced IL-8 expression at both mRNA and protein levels, up-regulated TF mRNA expression and TF activity, but down-regulated caspese-7 mRNA and p-p38 MAPK levels in SW620 cells. The effects of factor Ⅶa were not only blocked by anti-TF but also by anti-PAR2 antibodies. Conclusion Factor Ⅶa binds to TF on cell surface, forming a complex which activates PAR2, then provoking IL-8 and TF expression, and suppresses caepase-7 expression, thus promotes the tumor cell proliferation and migration, p38 MAPK may negatively regulate this process.

关 键 词:结肠肿瘤    受体  AR2    因子Ⅶa    细胞增殖    Factor  Ⅶa    
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