Li San-Qiang, Hu Zhi-Hong, Zhu Sha, Wang Dong-Mei, Han Hong-Mei, Lu Hua-Jie
The Molecular Medicine Key Laboratory of liver Injury and Repair, Medical College, Henan University of Science and Technology, Luoyang, 471003, People's Republic of China.
Department of Microbiology Immunology, College of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 45001, People's Republic of China.
J Biochem Mol Toxicol. 2015 Sep;29(9):440-448. doi: 10.1002/jbt.21737. Epub 2015 Aug 21.
This study was undertaken to evaluate the effect of ADAM8 on the proliferation and apoptosis of hepatocytes and hepatoma carcinoma cells during hepatocellular carcinoma (HCC) progression. The expression of ADAM8 was significantly increased with good correlation of PCNA expression increasing and cells apoptosis decreasing during the progression of HCC in the liver of mice. Proliferation experiment in vitro showed that recombinant ADAM8 could induce the expression of PCNA in L02 cells, but not in HepG2 cells. Apoptosis experiment in vitro showed that recombinant ADAM8 did not induce or inhibit the expression of apoptosis-related factors Bcl2, Bax, and Caspase3 in L02 cells, but significantly induced the expression of Bcl2, inhibited the expression of Bax and Caspase3 in HepG2 cells. In conclusion, our study suggested that ADAM8 could promote the proliferation of normal hepatocytes and render hepatoma carcinoma cells more resistant to apoptosis to play important roles during the progression of HCC. ADAM8; Proliferation; Apoptosis.
本研究旨在评估ADAM8在肝细胞癌(HCC)进展过程中对肝细胞和肝癌细胞增殖及凋亡的影响。在小鼠肝脏HCC进展过程中,ADAM8的表达显著增加,与增殖细胞核抗原(PCNA)表达增加及细胞凋亡减少具有良好的相关性。体外增殖实验表明,重组ADAM8可诱导L02细胞中PCNA的表达,但对HepG2细胞无此作用。体外凋亡实验表明,重组ADAM8在L02细胞中未诱导或抑制凋亡相关因子Bcl2、Bax和Caspase3的表达,但在HepG2细胞中显著诱导Bcl2的表达,抑制Bax和Caspase3的表达。总之,我们的研究表明,ADAM8可促进正常肝细胞的增殖,并使肝癌细胞对凋亡更具抗性,在HCC进展过程中发挥重要作用。ADAM8;增殖;凋亡。