Huang Jian-Zhao, Xia Sui-Sheng, Ye Qi-Fa, Jiang Han-Ying
Department of Hepatobiliary Surgery, Daping Hospital, Third Military Medical University, Chongqing, Sichuan, 400042, P. R. China.
Ai Zheng. 2003 Jan;22(1):46-9.
BACKGROUND & OBJECTIVE: Inactivation of the tumor suppressor gene p16INK4a is one of the most common genetic alterations in human hepatocellular carcinomas (HCC), making it an ideal target gene for treatment of HCC. The objective of this study was to investigate the influence of wild p16 gene on the biological behavior of HCC.
HCC cell strains SNU-449 (loss of p16 protein expression) and HepG2.2. 15 (positive p16 protein expression) were respectively infected by a retrovirus expression vector of p16 gene (pcLXSN-p16). The stable p16 protein expression cell strains were selected. The biological behaviors of the p16 gene transfected HCC cells were observed.
SNU-449 with negative p16 protein expression demonstrated that pcLXSN-p16 treatment significantly inhibited cell growth (the amount of cells at G0-G1 phase increased). However, there was no treatment effect when pcLXSN-p16 was transfected in HepG2.2. 15 which has positive p16 protein expression. Subsequent study in a nude mouse model demonstrated that the p16 gene transfected SNU-449 had a lower succeeding rate of first time establishment of tumors and grew more slowly in the nude mice as compared with non-transfected SNU-449. Moreover, the nude mice inoculated with transfected SNU-449 had a longer survival time than those inoculated with non-transfected SNU-449.
The transfer of wild p16 gene can inhibit the proliferation and reduce the invasion ability of HCC cells with p16 negative expression, but can not affect the HCC cells with p16 positive expression.
肿瘤抑制基因p16INK4a失活是人类肝细胞癌(HCC)最常见的基因改变之一,使其成为HCC治疗的理想靶基因。本研究旨在探讨野生型p16基因对HCC生物学行为的影响。
分别用p16基因的逆转录病毒表达载体(pcLXSN-p16)感染HCC细胞株SNU-449(p16蛋白表达缺失)和HepG2.2.15(p16蛋白表达阳性)。筛选出稳定表达p16蛋白的细胞株。观察p16基因转染的HCC细胞的生物学行为。
p16蛋白表达阴性的SNU-449显示,pcLXSN-p16处理显著抑制细胞生长(G0-G1期细胞数量增加)。然而,将pcLXSN-p16转染到p16蛋白表达阳性的HepG2.2.15中时没有治疗效果。随后在裸鼠模型中的研究表明,与未转染的SNU-449相比,p16基因转染的SNU-449首次成瘤成功率较低,在裸鼠中生长较慢。此外,接种转染SNU-449的裸鼠存活时间比接种未转染SNU-449的裸鼠长。
野生型p16基因的转导可抑制p16表达阴性的HCC细胞的增殖并降低其侵袭能力,但对p16表达阳性的HCC细胞无影响。