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作 者:万强琨 何斌[1] 宋世龙[1] 江浩[1] WAN Qiang-kun;HE Bin;SONG Shi-long;JIANG Hao(Department of Radiotherapy,The First Affiliated Hospital of Bengbu Medical College,Bengbu Anhui 233004,China)
机构地区:[1]蚌埠医学院第一附属医院放疗科,安徽蚌埠233004
出 处:《蚌埠医学院学报》2023年第3期286-289,共4页Journal of Bengbu Medical College
基 金:蚌埠医学院自然科学研究重点项目(2021byzd063);卫生健康发展促进项目-肿瘤科研专项(BJHA-CRP-065)。
摘 要:目的:观察线粒体亚甲基四氢叶酸脱氢酶2(mitochondrial methylenetetrahydrofolate dehydrogenase 2,MTHFD2)基因表达对人前列腺癌PC3细胞侵袭和转移能力的影响。方法:人前列腺癌PC3细胞分为3组:空白对照组(ctrl组)、阴性对照组(si-NC组)及转染siRNA-MTHFD2组(si-MTHFD2组)。采用qRT-PCR法检测人正常前列腺上皮细胞RWPE-1以及前列腺癌PC3细胞中MTHFD2的mRNA表达,通过流式细胞术检测MTHFD2对PC3细胞凋亡的影响,通过划痕实验检测细胞迁移能力的变化,通过Transwell实验检测细胞侵袭能力的变化,采用Western blotting检测E-cadherin、Vimentin和N-cadherin蛋白表达变化。结果:前列腺癌PC3细胞较正常前列腺上皮细胞中MTHFD2表达水平升高(P<0.05),si-MTHFD2组MTHFD2 mRNA表达水平较ctrl组和si-NC组降低(P<0.05);si-MTHFD2组细胞迁移和侵袭能力较ctrl组和si-NC组降低(P<0.05);si-MTHFD2组E-candherin蛋白表达水平较ctrl组和si-NC组升高(P<0.05),Vimentin和N-cadherin蛋白表达水平较ctrl组和si-NC组降低(P<0.05)。结论:下调MTHFD2表达可增加前列腺癌细胞凋亡能力,抑制前列腺癌细胞迁移和侵袭能力。Objective:To investigate the effect of mitochondrial methylenetetrahydrofolate dehydrogenase 2(MTHFD2)on cell invasion and metastasis in prostate cancer PC3 cells.Methods:The prostate cancer PC3 cells were divided into 3 groups:blank control group(ctrl group),negative control group(si-NC group)and transfected siRNA-MTHFD2 group(si-MTHFD2 group).The mRNA expression of MTHFD2 in human normal prostate epithelial cells RWPE-1 and prostate cancer PC3 cells was detected by qRT-PCR.The apoptosis rate in different groups was detected by flow cytometry,the changes of cell migration ability were detected by scratch test,the changes of cell invasion ability were detected by Transwell test,and the changes of E-cadherin,Vimentin and N-cadherin protein expressions were detected by Western blotting.Results:The expression level of MTHFD2 in prostate cancer PC3 cells was significantly higher than that in normal prostate epithelial cells(P<0.05),and the mRNA expression level of MTHFD2 in si-MTHFD2 group was significantly lower than that in ctrl and si-NC groups(P<0.05).The results of cell scratch and invasion assay showed that the migration and invasion abilities in si-MTHFD2 group was significantly lower than in ctrl and si-NC groups(P<0.05).E-candherin protein expression level in si-MTHFD2 group was significantly higher than that in ctrl and si-NC groups(P<0.05),and the protein expression levels of vimentin and N-cadherin were significantly lower than those in ctrl and si-NC groups.Conclusions:Down-regulation of MTHFD2 expression can increase the apoptosis of prostate cancer cells and inhibit the migration and invasion of prostate cancer cells.
关 键 词:前列腺肿瘤 线粒体亚甲基四氢叶酸脱氢酶2 侵袭 转移
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