Bao Shideng, Ouyang Gaoliang, Bai Xuefang, Huang Zhi, Ma Chaoyu, Liu Ming, Shao Rong, Anderson Ryan M, Rich Jeremy N, Wang Xiao-Fan
The Key Laboratory for Cell Biology and Tumor Cell Engineering, The Ministry of Education of China, The School of Life Sciences, Xiamen University, Fujian 361005, China.
Cancer Cell. 2004 Apr;5(4):329-39. doi: 10.1016/s1535-6108(04)00081-9.
Molecular mechanisms associated with tumor metastasis remain poorly understood. Here we report that acquired expression of periostin by colon cancer cells greatly promoted metastatic development of colon tumors. Periostin is overexpressed in more than 80% of human colon cancers examined with highest expression in metastatic tumors. Periostin expression dramatically enhanced metastatic growth of colon cancer by both preventing stress-induced apoptosis in the cancer cells and augmenting endothelial cell survival to promote angiogenesis. At the molecular level, periostin activated the Akt/PKB signaling pathway through the alpha(v)beta(3) integrins to increase cellular survival. These data demonstrated that the survival-promoting function is crucial for periostin to promote tumor metastasis of colon cancer.
与肿瘤转移相关的分子机制仍知之甚少。在此我们报告,结肠癌细胞获得性表达骨膜蛋白极大地促进了结肠肿瘤的转移发展。在超过80%的所检测人类结肠癌中骨膜蛋白过度表达,在转移瘤中表达最高。骨膜蛋白的表达通过既防止癌细胞中应激诱导的凋亡又增强内皮细胞存活以促进血管生成,显著增强了结肠癌的转移生长。在分子水平上,骨膜蛋白通过α(v)β(3)整合素激活Akt/PKB信号通路以提高细胞存活率。这些数据表明,促进存活的功能对于骨膜蛋白促进结肠癌肿瘤转移至关重要。