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作 者:李鹏[1,2] 张艳婷[2] 胡莹[2] 何彩霞[1] 杨少奇[2]
机构地区:[1]宁夏医科大学,银川750004 [2]宁夏医科大学总医院消化内科,银川750004
出 处:《宁夏医科大学学报》2015年第4期397-399,412,F0004,共5页Journal of Ningxia Medical University
摘 要:目的探讨Toll样受体9(TLR9)激动剂未甲基化的胞嘧啶-鸟嘌呤核苷酸序列(Cp G-ODN)对Hep G2肝癌细胞增殖及侵袭的影响。方法应用不同浓度的Cp G-ODN作用于肝癌细胞株Hep G2不同时间,采用实时荧光定量PCR法检测Hep G2中TLR9mRNA表达情况,MTT法检测Hep G2细胞的增殖变化,Transwell法检测其侵袭能力变化。结果 Cp G-ODN组(4、16μg·m L-1)与阴性对照组比较可增加Hep G2细胞中TLR9mRNA的表达;Cp G-ODN(1、4、16μg·m L-1)激动TLR9后可促进Hep G2细胞增殖,且以48h最为显著,并存在剂量依赖关系;Cp G-ODN(4、16μg·m L-1)激动TLR9可增强Hep G2细胞的侵袭能力(P均<0.05)。结论 TLR9表达上调可促进肝癌细胞增殖和侵袭。Objective To investigate the influence of the activator Cp G- ODN of TLR9 on the proliferation and invasion of hepatocellular cancer cells Hep G2. Methods Cp G- ODN with different concentration was administered to the hepatocellular cancer cells Hep G2. The expression of TLR9 mRNA was detected by real-time PCR and the proliferation of Hep G2 cells were determinded by MTT assay while the changes of invasion ablity were monitored by transwell assay. Results Cp G- ODN( 4,16μg·m L^-1) could significantly increase the TLR9 mRNA expression level compared with the negative control group. The proliferation of Hep G2 cells could be promoted when TLR9 was activated by Cp G- ODN( 1,4,16μg·m L^-1) and the most obvious change was at the 48 h point,which was a dose- dependent manne. The invasion ability of Cp G- ODN( 4,16μg·m L^-1) was significantly enhanced by TLR9( P〈0. 05). Conclusion Upregulation of TLR9 can promote proliferation and invasion in hepatocellular cancer cells.
关 键 词:TOLL样受体9 肝癌细胞 HEP G2 胞嘧啶-鸟嘌呤核苷酸序列
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