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In vitro and in vivo evidence of metallopanstimulin-1 in gastric cancer progression and tumorigenicity
作者姓名:王运伟  瞿颖  李建芳  朱正纲
作者单位:Department of General Surgery Shanghai Institute of Digestive Surgery,Ruijin Hospital,School of Medicine,Shanghai Jiaotong University,Department of General Surgery,Shanghai Institute of Digestive Surgery,Ruijin Hospital,School of Medicine,Shanghai Jiaotong University,Department of General Surgery,Shanghai Institute of Digestive Surgery,Ruijin Hospital,School of Medicine,Shanghai Jiaotong University,Department of General Surgery,Shanghai Institute of Digestive Surgery,Ruijin Hospital,School of Medicine,Shanghai Jiaotong University,Shanghai 200025,China,Shanghai 200025,China,Shanghai 200025,China,Shanghai 200025,China
基金项目:Hi-Tech Research and Development Program of China-“863”Program,2002CB713700,National Basic ResearchProgram of China-“973”Program,2002CB713700.
摘    要:Purpose:The metallopanstimulin-1(MPS-1)gene is a growth factor-inducible gene,which is highly expressed in many human cancers and may be involved in the progression towards tumor malignancy.However,it is unclear whether MPS-1 plays any role in gastric cancer development or progression.Our studies were designed to clarify the MPS-1 expression pattern and to explore its potential role in gastric cancer.Experimental Design:The expression pattern of MPS-1 was determined in primary gastric cancer specimens and gastric cancer cell lines via immunohistochemistry and Western blotting.To investigate the functional significance of MPS-1 expression,three small interfering RNA(siRNA)expression plasmids were constructed and transfected into gastric cancer cell line SGC7901.The stable cell lines transfected with the siRNA targeting MPS-1 mRNA plasmids were selected and the biological features of these cells were examined.Results:MPS-1 was overexpressed in 86% of the gastric cancer tissues and all gastric cancer cells.In addition,MPS-1 expression was significantly increased and corresponded with the tumor-node-metastasis clinical stage,and was significantly higher in the late stage(P<0.01).The MPS-1 expression level was significantly decreased in the transfected cells with MPS-1-specific siRNA expression plasmid pRNAT-133.Furthermore,the stable transfected cancer cells exhibited an increase in the incidence of spontaneous apoptosis and a decrease in growth ability and tumorigenicity in nude mice.Conclusions:These results provide strong evidence that MPS-1 plays an important role in gastric cancer cell proliferation and development,and suggests that MPS-1 is a promising target for gastric cancer treatment.

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