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The inhibition of apoptosis of hepatoma cells induced by HBx is mediated by up-regulation of survivin expression

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To investigate the effect of HBx on expression of survivin in hepatoma cells and mechanisms of inhibition of apoptosis on hepatoma cells induced by HBx, the expression plasmid pHAHBx encoding full length of HBx was transfected into HepG2 cells and the transformed cells were identified by RT-PCR. The expression of survivin both in HepG2 cells and HBx-transfected cells was examined with RT-PCR. The nude mice model of hepatoma was established by injecting HepG2 cells and HBx-transfected cells into the flank of nude mice subcutaneously. The expression level of survivin both in HepG2 formed tumors and HBx-transfected cell-formed tumors in nude mice was examined with Western-blot. The TUNEL assay was used to detect the apoptotic cells of tumor tissues in nude mice after intraabdominal chemotherapy with adriamycin. The results indicated that the amplification of survivin in HBx-transfected HepG2 cells was up-regulated when compared with that in non-transfected cells. Western-blot showed that the tumor cells expressing HBx in nude mice had a positive band of survivin expression and the tumor cells without HBx expression had no positive band. The result of TUNEL assay showed that there were less apoptotic cells in tumor tissues expressing HBx than that in control group cells. It was concluded that HBx could upregulate the expression of survivin in hepatic carcinoma cells which can inhibit apoptosis of hepatic carcinoma cells induced by adriamycin.

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LI Donghua, male, born in 1961, Associate Professor

This project was supported by the National Natural Science Foundation of China (No. 30371395) and Key Clinical Research Projects of the Ministry of Public Health (2001–2003).

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Donghua, L., Xiaoping, C. & Wanguang, Z. The inhibition of apoptosis of hepatoma cells induced by HBx is mediated by up-regulation of survivin expression. Current Medical Science 23, 383–386 (2003). https://doi.org/10.1007/BF02829424

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  • DOI: https://doi.org/10.1007/BF02829424

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