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作 者:杨冬华[1] 张鸣青[1] 杜江[2] 徐重[2] 梁巧明[2] 毛积芳[3] 覃汉荣[1] 范子荣[1]
机构地区:[1]第一军医大学珠江医院消化科,广州510282 [2]第一军医大学珠江医院分子生物学实验室,广州510282 [3]上海第二军医大学生物化学研究室
出 处:《中华肝脏病杂志》1999年第1期39-41,共3页Chinese Journal of Hepatology
基 金:广东省自然科学基金!NO.940319
摘 要:研究人胰岛素样生长因子Ⅱ(IGF-Ⅱ)反义RNA对肝癌细胞株SMMC-7721的抑制效应。方法人IGF-ⅡcDNA0.1kb反向插人真核细胞表达载体pcNA3,获得IGF-Ⅱ反义RNA表达载体pIGF-ⅡAS,将其导人人肝癌细胞株SMMC-7721,观察软琼脂培养集落形成的能力。流式细胞仪(FCM)测定pIGF-ⅡAs表达IGF-Ⅱ反义RNA对SMMC-7721细胞生长的影响。结果转导人pIGF-ⅡAs的SMMC-7721细胞,不能在软琼脂上形成集落,FCMM实导人PIGF-ⅡAs细胞S期增多,而对照组SMMC-7721细胞和带DCDNA3空载体的SMMC-7721细胞则无明显变化.结论pIGF-ⅡAS&义RNA体外可抑制肝癌细胞株SMMC-7721的致瘤性。Objetive Inhibitory effect of insulin like growth factor II (IGF- II ) antisense RNA onmalignant phenotype of hepatic cancer cells was studied. Methods A 0.lkb cDNA of human IGF- wasreversely inserted into a eukaryotic expression vector of pcDNA3 and an IGF antisense RNA expressionvector of PIGF- As was obtained. The pIGF- As was then introduced into human hepatic cancer cellline SMMC-7721. The effect of IGF- antisense RNA Which was expressed by pIGF- As on SMMC7721 cell cycles progression was measured with FCM. Results The coloning formation in dependent assay of SMMC-7721 cells with pIGF-As was significantly decreased by comparision withcontrol groups of SMMC-7721 Cells and SMMC-7721 cells transfected with pcDNA3 vector alone. FCManalysis showed that the s phase of cell cycles for SMMC-7721 cells with pIGF-As was increased, butthere were no obvious changes in the control groupe of SMMC-7721 cells and SMMC-7721 cells withpcDNA3. Conclusion The pIGF-As of IGF- antisense RNA acts as an inhibitor on carcinogenesis ofthe SMMC-7721 Cells in vitro.
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