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作 者:林楠[1] 唐亚军[1] 王旭天 方和平[1] 周正[1] 许瑞云[1]
机构地区:[1]中山大学附属第三医院肝胆外科,广州510630
出 处:《中华实验外科杂志》2015年第6期1317-1319,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81272642);教育部博士点基金资助项目(20110171110070)
摘 要:目的 利用裸鼠肝癌模型观察活化态肝星状细胞(aHSC)分泌血管生成素-1(Ang-1)对肝癌生长及微血管生成的影响.方法 建立裸鼠肝癌模型,实验组为肝星状细胞株(LX-2)与肝癌细胞株(HepG2)细胞混合注射(1∶1,100μl,细胞浓度:5 × 109/L),干预组为Ang-1表达抑制的LX-2细胞株(LX-2-siAng-1)与HepG2细胞混合注射;对照组为HepG2细胞单独注射.4周后测量肿瘤体积,同时检测Ang-1、Ang-2与血管标志物CD34的mRNA与蛋白表达.结果 实验组肿瘤生长体积明显大于对照组[(445.3 ±43.2) mm3比(167.8 ±22.9) mm3,P<0.05),干预组肿瘤生长体积相对实验组明显减小[(235.4±16.5)mm3比(445.3±43.2) mm3,P<0.05];Ang-1及血管标志物CD34在肿瘤组织中分布一致;实验组中Ang-1、CD34的蛋白及mRNA表达明显高于干预组及对照组(P<0.05).结论 aHSC可通过分泌Ang-1促进肝细胞癌生长,并促进肝癌血管生成.Objective To investigate the effects of activated hepatic stellate cells (aHSCs) on proliferation and angiogenesis in nude mice hepatocellular carcinoma (HCC) model through secretion of angiopoietin-1.Methods A hepatocellular carcinoma model was established by means of subcutaneous injection on nude mice.In the experimental group,the mixture of LX-2 and HepG2 cells (1∶1,100 μl in total,and 5 × 109/L of both cell lines) were given.In the the intervention group,the mixture of LX-2 (siAng-1) and HepG2 (1∶1,100 μl in total,and 5 × 109/L of both cell lines).In the control group,only HepG2 cells were given (100 μl in total,5 × 109/L).The growth of tumors was observed,and the tumors were resected after four weeks.Meanwhile,the protein and mRNA expression levels of Ang-1,Ang-2 and CD34 were detected.Results The tumor size in experimental group was significantly bigger than in control group [(445.3 ± 43.2) mm3 vs.(167.8 ± 22.9) mm3,P < 0.05],and the growth rate was decreased when Ang-1 mRNA was silenced [(445.3 ± 43.2) mm3 vs.(235.4 ± 16.5) mm3,P < 0.05].Ang-1 was consistent to CD34 in distribution,and the expression levels of CD34 and Ang-1 in experimental group were significantly higher than those in the intervention group and control group (both P < 0.05).Conclusion aHSC can promote both the growth of hepatoma cells and angiogenesis in hepatocellular carcinoma through secretion of angiopoietin-1.
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