首页 | 本学科首页   官方微博 | 高级检索  
     

FATE/BJ-HCC-2基因转染对肿瘤细胞生物学行为的影响
引用本文:杨小昂,邵启祥,钱晓萍,李燕,庞学雯,陈慰峰. FATE/BJ-HCC-2基因转染对肿瘤细胞生物学行为的影响[J]. 河南医学研究, 2006, 15(4): 305-311
作者姓名:杨小昂  邵启祥  钱晓萍  李燕  庞学雯  陈慰峰
作者单位:河南省医学科学研究所,河南郑州,450052;江苏大学医学技术学院免疫学系,镇江,212001;北京大学医学部免疫学系,北京,100083
摘    要:目的:观察FATE/BJ-HCC-2基因对肿瘤细胞生物学行为的影响,探讨FATE/BJ-HCC-2与肿瘤进展之间的关系。方法:将FATE/BJ-HCC-2基因转染肝癌细胞系Bel-7402细胞,3H-TdR掺入法和Transwell实验对转染细胞的增殖和侵袭能力进行检测;PCR方法检测细胞内的骨桥蛋白(OPN)和整合素连接激酶(ILK)基因的表达水平。结果:细胞增殖实验结果显示FATE/BJ-HCC-2转染肿瘤细胞的3H-TdR掺入值显著高于Mock细胞的掺入值,统计学分析二者差别有显著性意义(P<0.01)。FATE/BJ-HCC-2基因表达促进肝癌细胞系Bel-7402细胞的增殖,并且这种增殖效应可被特异性抗-FATE/BJ-HCC-2抗体所阻断。Transwell实验显示,转染FATE/BJ-HCC-2的细胞,其穿膜数量明显比对照组多,差别有显著的统计学意义(P<0.01)。对肿瘤细胞转移相关的细胞信号分子进行检测发现,骨桥蛋白(OPN)和整合素连接激酶(ILK)基因的表达水平上调。结论:肿瘤细胞获得FATE/BJ-HCC-2基因表达后其增殖和侵袭能力增强,FATE/BJ-HCC-2基因表达可能与肿瘤细胞的转移有一定关系。提示CT抗原的表达不仅仅是肿瘤发生中的伴随产物,它可能在肿瘤的发生发展过程中起到一定作用。

关 键 词:CT抗原  FATE/BJ-HCC-2  生物学功能  基因转染
文章编号:1004-437X(2006)04-0305-07
收稿时间:2006-11-13
修稿时间:2006-12-07

Effects of FATE/BJ-HCC-2 gene transfection on biological behavior of tumor cells
YANG Xiao-ang,SHAO Qi-xiang,QIAN Xiao-ping,LI Yan,PANG Xue-wen,CHEN Wei-feng. Effects of FATE/BJ-HCC-2 gene transfection on biological behavior of tumor cells[J]. Henan Medical Research, 2006, 15(4): 305-311
Authors:YANG Xiao-ang  SHAO Qi-xiang  QIAN Xiao-ping  LI Yan  PANG Xue-wen  CHEN Wei-feng
Affiliation:1. ttenan Institute of Medical Sciences, Zhengzhou University, Zhengzhou 450052; 2. Department of Immunology, School of Medical Technology, Jiangsu University, Zhenjiang 212001 3. Department of Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100083, China
Abstract:Objective:To elucidate the role of FATE/BJ-HCC-2 gene in tumorigenesis and cancer cell metastasis and its effects on biological behavior of tumor cells.Methods: The FATE/BJ-HCC-2 gene was stably transfected into HCC cell line Bel-7402 cells.The cell proliferation and invasive ability were detected with -thymidine uptake and transwell migration assays.mRNA expression of osteopontin(OPN) and integrin linked kinase(ILK) was analysed in FATE/BJ-HCC-2 gene-transfected cells by PCR.Results: The cell proliferation assay showed that -thymidine uptake in FATE/BJ-HCC-2 gene transfected tumor cells was signicantly higher than that in mock control cells.Statistical analysis indicated that the difference is significant(P<0.01).FATE/BJ-HCC-2 gene transfection enhanced Bel-7402 cells' proliferation.Importantly,this FATE/BJ-HCC-2 enhanced proliferation could be specifically blocked by anti-FATE/BJ-HCC-2 antibody.The result of transwell migration assay showed that the number of penetrated cells in the FATE/BJ-HCC-2 gene-transfected group was much more than that in control group.The difference between two groups is significant(P<0.01).Subsequent studies examining tumor metastasis associated molecules showed that mRNA expression of osteopontin(OPN) and integrin linked kinase(ILK) was upregulated in FATE/BJ-HCC-2 gene-transfected cells.Conclusion: The FATE/BJ-HCC-2 gene-transfected cells appear to have more potent proliferation and invasive ability and the expression of FATE/HCC-2 gene is related to metastasis of tumor cells.In general,our discoveries imply that cancer/testis(CT) antigens may play critical roles in tumorigenesis and tumor progression.
Keywords:cancer/testis antigen  FATE/BJ-HCC-2  biological function  gene transfection
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号