Wang Qun, Liu Quan-yan, Liu Zhi-Su, Qian Qun, Sun Quan, Pan Ding-yu
Department of General Surgery, Zhongnan Hospital of Wuhan University, Hubei Province, PR China.
J Exp Clin Cancer Res. 2008 Nov 21;27(1):72. doi: 10.1186/1756-9966-27-72.
RNA interference (RNAi) has been successfully applied in suppression of hepatic cancer genes. In hepatocelluar carcinoma cell, one methionine adenosyltransferase (MAT) isozyme, MATII was found to have two catalytic subunits which were encoded by MAT2A and MAT2beta respectively. During tumorigeness of hepatocelluar carcinoma, expressions of the two genes were discovered to be increased combining with a switch of MAT (form MATI to MATII), To figure out the role played by MATII in hepatic cancer, In this study, for the first time we established a dual small interfering RNA (siRNA) expression system, which could simultaneously express two different siRNA molecules specifically targeting two genes. To test the effectiveness of this system, we applied this approach to express simultaneously two different siRNA duplexes that specifically target MAT2A and MAT2beta genes of hepatocelluar carcinoma respectively in HepG2 cell. Results indicated that dual siRNA could simultaneously inhibit the expression of MAT2A and MAT2beta gene by 89.5% and 97.8% respectively, In addition, dual siRNA molecules were able to significantly suppress growth of hepatocelluar carcinoma cell in vitro as well as induce apoptosis which was involved in arrest cell cycle at the G1/S checkpoint and the expressions of p21, p27 and Bax.
RNA干扰(RNAi)已成功应用于肝癌基因的抑制。在肝癌细胞中,发现一种甲硫氨酸腺苷转移酶(MAT)同工酶MATII有两个催化亚基,分别由MAT2A和MAT2β编码。在肝癌发生过程中,发现这两个基因的表达增加,同时伴随着MAT(从MATI转变为MATII)的转换。为了弄清楚MATII在肝癌中的作用,在本研究中,我们首次建立了一个双小干扰RNA(siRNA)表达系统,该系统可以同时表达两个特异性靶向两个基因的不同siRNA分子。为了测试该系统的有效性,我们应用这种方法在HepG2细胞中同时表达分别特异性靶向肝癌MAT2A和MAT2β基因的两种不同的siRNA双链体。结果表明,双siRNA可以分别同时抑制MAT2A和MAT2β基因的表达89.5%和97.8%。此外,双siRNA分子能够在体外显著抑制肝癌细胞的生长,并诱导细胞凋亡,这涉及到细胞周期在G1/S检查点的阻滞以及p21、p27和Bax的表达。