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机构地区:[1]泸州医学院医学分子生物学实验室,四川泸州646000 [2]泸州医学院病理学教研室,四川泸州646000
出 处:《重庆医学》2012年第34期3583-3585,共3页Chongqing medicine
基 金:四川省科技厅科研项目(07JY029-134);四川省教育厅科研项目(07ZB110)
摘 要:目的构建骨桥蛋白(OPN)基因真核表达载体,转染人结肠癌细胞SW480,研究其对SW480细胞增殖及生存能力的作用机制。方法构建重组表达载体pEGFP-N1/OPN,转染人结肠癌SW480细胞。采用RT-PCR及免疫印迹法(Westernblotting)分别检测SW480细胞OPN基因及蛋白表达量;Cell Counting Kit-8(CCK-8)测定细胞增殖;软琼脂克隆形成实验观察细胞的锚定非依赖性生长能力。Western blotting检测脆性组氨酸三联体基因(FHIT)和蛋白激酶B(PKB/Akt)蛋白在SW480细胞中的表达。结果重组质粒pEGFP-N1/OPN转染SW480后,OPN基因获得很好转录,OPN蛋白表达增高,细胞增殖率(光吸收值)显著高于转染阴性组(P<0.05),细胞软琼脂克隆形成速度增快,数量明显多于对照组和空载体组(P<0.05);FHIT蛋白在实验组表达降低,Akt蛋白在各组中的表达无显著性差异。结论 OPN基因通过抑制FHIT基因表达,促进SW480细胞增殖、独立存活能力。Objective To construct an OPN eukaryotic expression vector,and evaluate its effects on proliferation and survival in SW480 colon cancer cells in vitro,exploring the possible mechanism. Methods OPN gene was cloned into the eukaryotic expression vector pEGFP-N1 ,after sequencing, the vector was then transfected into SW480 cells. The OPN gene and protein expression in transfected cells were demonstrated by RT PCR and Western blotting respectively. The impact on proliferation in transfected SW480 cells were investigated by CCK-8 method,anchorage independent growth was measured using soft agar assay. Western blot- ting was used to analyzing the protein of fragile histidine triad gene(FHIT) and protein kinase B(PKB/Akt). Results The levels of OPN gene and protein in colon cancer SW480 cells were distinctly increased after transfeetion with pEGFP-N1/OPN. The OD450 value of OPN transfection group was higher than negative control group showed by CCK-8 method(P〈0.05). They could also sig- nificantly increase anchorage independent growth in vitro. FHIT protein was significantly increased in SW480 cells transfected with pEGFP-N1/OPN. Conclusion In SW480 colon cancer cells,OPN was involved in promotion proliferation and survival, by regula- ting the FHIT protein expression.
关 键 词:骨桥蛋白质 结肠肿瘤 脆性组氨酸三联体基因
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