Primary functional identification of gene TMSG-1

被引:7
作者
Ma, CS
Ning, JY
You, JF
Liu, L
Wang, JL
Cui, XL
Wu, BQ
Zheng, J [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Anal Ctr Med & Hyg, Beijing 100083, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Dept Pathol, Beijing 100083, Peoples R China
来源
SCIENCE IN CHINA SERIES C-LIFE SCIENCES | 2003年 / 46卷 / 06期
基金
中国国家自然科学基金;
关键词
prostate cancer; gene transfection; pH; apoptosis;
D O I
10.1360/02yc0159
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
TMSG-1 was a tumor metastasis-related gene identified using mRNA differential display, whose expression level was lower in cancer cell lines with higher metastatic potential and in tumor tissue with metastasis. TMSG-1 was transfected to prostate cancer cell line (PC-3M-1 E8) with high metastatic potential to observe the effects of increased expression of TMSG-1 on V-ATPase activity, intracellular pH and cell apoptosis. Subcellular localization of the encoded protein of TMSG-1 was determined by using GFP. Results showed that there were no differences of V-ATPase activity among parental PC-3M-1E8 cell line, pcDNA3 transfectant and anti-TMSG-1 transtectant, whereas the V-ATPase activity was significantly higher in TMSG-1 transfectant than that in parental PC-3M-1 E8 cell line, pcDNA3 transfectant and Anti-TMSG-1 transfectant (p<0.001). Intracellular pH (pHi) was detected by using the pH-dependent fluorescence probe BECEF Results showed the pHi was significantly increased in TMSG-1 transfectant. Cell apoptosis assay demonstrated cell apoptosis was significantly higher in -1 transfectant (p<0.01) and BCL2 expression was down regulated. Subcellular localization of TMSG-1 protein showed TMSG-1 was a transmembrane protein, which predicted TMSG-1 protein was located in cytoplasm system, such as endoplasmic reticulum and mitochondrial. These results indicated TMSG-1 up regulation in prostate cancer cell line could promote V-ATPase activity, increase pHi and cell apoptosis, and inhibit the expression of BCL2.
引用
收藏
页码:641 / 650
页数:10
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