Enhanced expression of trophinin promotes invasive and metastatic potential of human gallbladder cancer cells

被引:20
作者
Chang, Xin-Zhong [3 ]
Yu, Jie [2 ]
Zhang, Xue-Hui [3 ]
Yin, Jian [3 ]
Wang, Tao [1 ]
Cao, Xu-Chen [3 ]
机构
[1] Shantou Univ, Shantou 515063, Peoples R China
[2] Weifang Univ, Weifang 261061, Peoples R China
[3] Tianjin Univ, Canc Hosp & Inst, Tianjin 300060, Peoples R China
基金
中国博士后科学基金;
关键词
Gallbladder cancer; Invasion; Metastasis; Trophinin; ETS-1; GENE; INTEGRIN; TASTIN; INVOLVEMENT; ADHESION; BYSTIN; MMP-9; IDENTIFICATION; IMPLANTATION; TROPHOBLAST;
D O I
10.1007/s00432-008-0492-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To study effects of trophinin on the metastatic potential of human gallbladder cancer cells and its potential mechanism. Expression of trophinin in the highly metastatic GBC-SDHi cells was investigated by real time RT-PCR and western blot. Recombinant expression plasmid vector of the human trophinin gene was constructed and transfected into GBC-SD cells. Effects of trophinin on the invasion of GBC-SD cells were investigated by adhesion assay and invasion assay in vitro. The siRNA was used to down-regulate the expression of trophinin. Some genes related to the invasion and metastasis of cancer were determined by real time RT-PCR and western blot. The pulmonary metastasis regulated by trophinin was determined in the nude mice. Overexpression of trophinin in GBC-SDHi cells was confirmed compared with its parental counterparts. Up-regulation of trophinin enhanced the in vitro invasion in the GBC-SD/TRO cells. The enhancement was associated with increasing integrin alpha 3, MMP-7, MMP-9, and Ets-1 expression. The results were further demonstrated by RNA interference experiment in vitro. In in vivo study, we also demonstrated that trophinin-transfected gallbladder cancer cells had more pulmonary metastases than the vector-transfected one or its parental counterparts. Overexpression of trophinin leads to a more invasive phenotype and metastatic potential in human gallbladder cancer, at least in part, through regulating integrin alpha 3, MMP-7, MMP-9, and Ets-1 expression.
引用
收藏
页码:581 / 590
页数:10
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