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[阻断人肝再生增强因子(hALR)表达对肝癌细胞系HepG2增殖的抑制作用]

[Inhibitory effect of blocking expression of human augmenter of liver regeneration (hALR) on proliferation of hepatocellular carcinoma cell line HepG2].

作者信息

Tang Lin, Sun Hang, Zhang Lin, Guo Hui, Zhang Ling, Liu Qi

机构信息

Laboratory of Molecular Biology for Infectious Disease, Institute for Viral Hepatitis, Chongqing University of Medical Sciences, Chongqing, 400010, P. R. China.

出版信息

Ai Zheng. 2006 Jun;25(6):671-6.

Abstract

BACKGROUND & OBJECTIVE: Human augmenter of liver regeneration (hALR) is highly expressed in hepatocellular carcinoma (HCC), but rarely expressed in normal liver cells. ALR could stimulate the proliferation of HCC cell line in vitro, but has no effect on normal hepatocytes. This study was to investigate the inhibitory effect of blocking the expression of hALR on the proliferation of HCC cell line HepG2 using small interfering RNA (siRNA) targeting ALR and anti-ALR monoclonal antibody (McAb).

METHODS

RNA interference (RNAi) plasmid pSIALR-A targeting hALR cDNA and control plasmid pSIALR-B were constructed and transfected into HepG2 cells, respectively. After transfection, the expression of green fluorescent protein was observed under a fluorescent microscope to calculate transfection efficiency, the protein level of hALR was measured by immunocytochemistry, meanwhile, the expression of hALR mRNA was detected by reverse transcription-polymerase chain reaction (RT-PCR). (3)H-TdR incorporation approach was performed to detect the proliferation of HepG2 cells after transfection and after neutralization with anti-hALR McAb.

RESULTS

hALR was expressed in HepG2 cells. Plasmids pSIALR-A and pSIALR-B were successfully constructed. Both immunocytochemistry and RT-PCR showed that pSIALR-A inhibited the expression of hALR in HepG2 cells significantly by 83% as compared with pSIALR-B. pSIALR-A specifically inhibited the growth of HepG2 cells after transfection. (3)H-TdR incorporation of pSIALR-A/HepG2 cells was significantly lower than that of pSIALR-B/HepG2 cells (67 687+/-6 548 vs. 104 807+/-5 713, P<0.05). Anti-hALR McAb markedly inhibited the autonomous growth of HepG2 cells (P<0.05).

CONCLUSIONS

hALR is highly expressed in HepG2 cells. The short interfering RNA targeting hALR gene could specifically suppress the expression of hALR, and subsequently inhibit the growth of HepG2 cells. Anti-hALR McAb could partially inhibit the autonomous growth of HepG2 cells.

摘要

背景与目的

人肝再生增强因子(hALR)在肝细胞癌(HCC)中高表达,而在正常肝细胞中很少表达。ALR可在体外刺激HCC细胞系增殖,但对正常肝细胞无作用。本研究旨在利用靶向ALR的小干扰RNA(siRNA)和抗ALR单克隆抗体(McAb),探讨阻断hALR表达对HCC细胞系HepG2增殖的抑制作用。

方法

构建靶向hALR cDNA的RNA干扰(RNAi)质粒pSIALR - A和对照质粒pSIALR - B,并分别转染至HepG2细胞。转染后,在荧光显微镜下观察绿色荧光蛋白的表达以计算转染效率,采用免疫细胞化学法检测hALR的蛋白水平,同时用逆转录 - 聚合酶链反应(RT - PCR)检测hALR mRNA的表达。采用³H - TdR掺入法检测转染后及用抗hALR McAb中和后的HepG2细胞增殖情况。

结果

hALR在HepG2细胞中表达。成功构建了质粒pSIALR - A和pSIALR - B。免疫细胞化学和RT - PCR均显示,与pSIALR - B相比,pSIALR - A显著抑制HepG2细胞中hALR的表达达83%。转染后pSIALR - A特异性抑制HepG2细胞生长。pSIALR - A/HepG2细胞的³H - TdR掺入量显著低于pSIALR - B/HepG2细胞(67 687±6 548 vs. 104 807±5 713,P<0.05)。抗hALR McAb显著抑制HepG2细胞的自主生长(P<0.05)。

结论

hALR在HepG2细胞中高表达。靶向hALR基因的短干扰RNA可特异性抑制hALR的表达,进而抑制HepG2细胞的生长。抗hALR McAb可部分抑制HepG2细胞的自主生长。

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