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作 者:贾欣永[1] 李杰[1] 徐宗珍[1] 韩旭[1] 张强波[1] 时昌文[1]
出 处:《中国现代普通外科进展》2007年第2期153-155,共3页Chinese Journal of Current Advances in General Surgery
基 金:山东省自然科学基金资助项目(2004ZX09)
摘 要:目的:探讨整合素αV、β3反义基因对种植性肝癌血管生成的阻抑作用。方法:建立裸鼠肝癌模型,将反义基因表达载体αV/pcDNA3、β3/pcDNA3分别以αV、β3及αVβ3联合形式瘤内转染,同时设载体空壳组对照,检测整合素αV、β3蛋白及肿瘤组织微血管密度(MVD)的改变。结果:(1)实验组较对照组αV、β3蛋白表达显著降低(P<0.05);实验组之间差异无统计学意义(P>0.05)。(2)对照组、αV组、β3组、αVβ3组MVD分别为(17.53±1.88)、(16.06±1.92)、(15.83±2.00)、(14.86±1.69)条,αVβ3组与αV组、β3组及实验组与对照组之间MVD差异均有统计学意义(P<0.05)。结论:整合素αV、β3反义基因可明显下调整合素αV、β3蛋白表达,抑制肿瘤血管生成,联合应用效果更加显著。Objective: To investigate whether antisense integfin αV and β 3 gene has anti-angiogenesis activity in implanting hepatocellular arcinomas in nude mice. Methods: The antisense integrin αV and β 3 expression vectors were injected into HepG2 hepatomas established in nude mice, and tumorangiogenesis, integrin αV, integrin β 3, CD31 expressions were examined by immunostaining. Results: Gene transfer of antisenseintegrin αV and integrin β 3 expression vec- tors downregulated αV and β 3 protein expression inHepG2 tumors established in nude mice, and inhibited their vascularization. The median of microvessel density (MVD) in control, As-V, As- β 3 and As-αV β 3 group were 17.53,16.06,15.83 and 14.86 respectively, Antisense αV inhibited tumor angiogenesis more strongly than antisense 15 3; however antisense therapy that simultaneously targeted both integrin subunits was more effective than the respective monotherapies.Conclusions: Antisense gene therapy targeting αV and β3 integrins inhibited implantinghepatocellular arcinomas angiogenesis, which can be considered as an approach to treat hepatoceuular carcinomas.
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