CAJ | 학술논문

目的观察过表达人滋养层细胞表面抗原-2(TROP-2)基因对人前列腺癌细胞的迁移和侵袭及上皮-间充质转化的影响.方法将TROP-2基因克隆到真核表达载体pcDNA3.1,构建TROP-2基因过表达真核表达质粒.PC-3细胞分为3组:空白对照组、空载对照组和TROP-2过表达组.转染PC-3细胞后,采用Western blot法观察TROP-2蛋白表达,采用Transwell方法检测癌细胞迁移和侵袭能力,采用Western blot法检测癌细胞E-钙黏蛋白和N-钙黏蛋白表达.结果成功构建TROP-2基因真核表达质粒.与空白对照组和空载对照组比较,TROP-2过表达组TROP-2蛋白明显升高.Transwell迁移实验结果显示,空白对照组、空载对照组和TROP-2过表达迁移细胞数分别为(132.6±2.2)、(130.8±1.8)和(189.6±2.6)个.与空白对照组比较,差异有统计学意义(P＜0.01);Transwell侵袭试验显示,空白对照组、空载对照组和TROP-2过表达迁移细胞数分别为(118.16±1.96)、(117.52±1.85)和(166.38±1.65)个.与空白对照组比较,差异有统计学意义(P＜0.01).Western blot结果显示,与空白对照组比较,TROP-2过表达细胞组E-钙黏蛋白表达降低,而N-钙黏蛋白表达增高.结论 TROP-2过表达可促进入前列腺癌细胞迁移和侵袭能力,其机制可能与促进上皮-间充质转化有关.
목적 관찰과표체인자양층세포표면항원-2(TROP-2)기인대인전렬선암세포적천이화침습급상피-간충질전화적영향.방법 장TROP-2기인극륭도진핵표체재체pcDNA3.1,구건TROP-2기인과표체진핵표체질립.PC-3세포분위3조:공백대조조、공재대조조화TROP-2과표체조.전염PC-3세포후,채용Western blot법관찰TROP-2단백표체,채용Transwell방법검측암세포천이화침습능력,채용Western blot법검측암세포E-개점단백화N-개점단백표체.결과 성공구건TROP-2기인진핵표체질립.여공백대조조화공재대조조비교,TROP-2과표체조TROP-2단백명현승고.Transwell천이실험결과현시,공백대조조、공재대조조화TROP-2과표체천이세포수분별위(132.6±2.2)、(130.8±1.8)화(189.6±2.6)개.여공백대조조비교,차이유통계학의의(P＜0.01);Transwell침습시험현시,공백대조조、공재대조조화TROP-2과표체천이세포수분별위(118.16±1.96)、(117.52±1.85)화(166.38±1.65)개.여공백대조조비교,차이유통계학의의(P＜0.01).Western blot결과현시,여공백대조조비교,TROP-2과표체세포조E-개점단백표체강저,이N-개점단백표체증고.결론 TROP-2과표체가촉진입전렬선암세포천이화침습능력,기궤제가능여촉진상피-간충질전화유관.
Objective To explore the effects of over-expression of trophoblast cell-surface antigens 2 (TROP-2) gene on the migration and invasion of human prostate cancer cells and the action mechanism.Methods The TROP-2 gene was cloned into the eukaryotic expression vector pcDNA3.1,and TROP-2 over-expression of eukaryotic gene expression plasmid was constructed.All PC-3 cells were divided into three groups:the control group (Con-A),empty vector control group (Con-B) and over-expression group TROP-2 (pcDNA3.1-TROP-2).After PC-3 cells in three groups were transfected with phosphate buffer (PBS),vector pcDNA3.1,or pcDNA3.1-TROP-2,the protein levels of TROP-2 were determined by Western blotting,respectively.The migration and invasion ability was evaluated by Transwell.The E-Cadherin and N-Cadherin protein expression in PC-3 cells was examined by Western blotting.Results TROP-2 gene eukaryotic expression vector was successfully constructed.The Western blotting showed that the expression levels of TROP-2 protein were greatly increased in PC-3 cancer cells transfected with pcDNA3.1-TROP-2.The Transwell migration assay revealed that the number of migrating cells in Con-A,Con-B,and pcDNA3.1-TROP-2 groups was 132.6 ±2.2,130.8 ± 1.8 and 189.6±2.6,respectively (P ＜ 0.01).The Transwell invasion assay indicated that the number of migrating cells in Con-A,Con-B,and pcDNA3.1-TROP-2 groups was 118.16 ± 1.96,117.52 ± 1.85 and 166.38 ± 1.65,respectively (P ＜ 0.01).As Compared with the Con-A group,the E-cadherin protein expression was decreased,and the N-cadherin protein expression was increased in PC-3 cancer cells transfected with pcDNA3.1-TROP-2.Conclusion TROP-2 overexpression can promote migration and invasion of human prostate cancer cells probably promoting the epithelial-mesenchymal transition.