中国免疫学杂志
中國免疫學雜誌
중국면역학잡지
CHINESE JOURNAL OF IMMUNOLOGY
2015年
9期
1242-1244
,共3页
王子航%李春实%康劲松%米旭光%刘磊
王子航%李春實%康勁鬆%米旭光%劉磊
왕자항%리춘실%강경송%미욱광%류뢰
乳腺癌%microRNA-199a/b-3p%迁移侵袭%细胞膜皱起%PAK4
乳腺癌%microRNA-199a/b-3p%遷移侵襲%細胞膜皺起%PAK4
유선암%microRNA-199a/b-3p%천이침습%세포막추기%PAK4
Breast cancer%microRNA-199a/b-3p%Migration and invasion%Membrane protrusion%PAK4
目的:探讨microRNA-199a/b-3p抑制乳腺癌细胞运动能力的机制。方法:在乳腺癌MDA-MB-231细胞中,转入miR-199a/b-3p mimcs,免疫印迹法检测PAK4的表达量变化;迁移和侵袭实验检测,超表达miR-199a/b-3p和干扰PAK4表达对乳腺癌迁移侵袭的影响;细胞膜皱起检测,超表达miR-199a/b-3p和干扰PAK4表达对乳腺癌细胞细胞膜皱起的影响。结果:在MDA-MB-231细胞中,超表达miR-199a/b-3p或干涉内源PAK4蛋白表达,均能下调细胞的迁移率、侵袭率和平均细胞膜皱起面积。结论:miR-199a/b-3p抑制乳腺癌细胞运动能力部分是通过抑制PAK4表达实现的,且miR-199a/b-3p具有抗乳腺癌迁移药物开发的潜质。
目的:探討microRNA-199a/b-3p抑製乳腺癌細胞運動能力的機製。方法:在乳腺癌MDA-MB-231細胞中,轉入miR-199a/b-3p mimcs,免疫印跡法檢測PAK4的錶達量變化;遷移和侵襲實驗檢測,超錶達miR-199a/b-3p和榦擾PAK4錶達對乳腺癌遷移侵襲的影響;細胞膜皺起檢測,超錶達miR-199a/b-3p和榦擾PAK4錶達對乳腺癌細胞細胞膜皺起的影響。結果:在MDA-MB-231細胞中,超錶達miR-199a/b-3p或榦涉內源PAK4蛋白錶達,均能下調細胞的遷移率、侵襲率和平均細胞膜皺起麵積。結論:miR-199a/b-3p抑製乳腺癌細胞運動能力部分是通過抑製PAK4錶達實現的,且miR-199a/b-3p具有抗乳腺癌遷移藥物開髮的潛質。
목적:탐토microRNA-199a/b-3p억제유선암세포운동능력적궤제。방법:재유선암MDA-MB-231세포중,전입miR-199a/b-3p mimcs,면역인적법검측PAK4적표체량변화;천이화침습실험검측,초표체miR-199a/b-3p화간우PAK4표체대유선암천이침습적영향;세포막추기검측,초표체miR-199a/b-3p화간우PAK4표체대유선암세포세포막추기적영향。결과:재MDA-MB-231세포중,초표체miR-199a/b-3p혹간섭내원PAK4단백표체,균능하조세포적천이솔、침습솔화평균세포막추기면적。결론:miR-199a/b-3p억제유선암세포운동능력부분시통과억제PAK4표체실현적,차miR-199a/b-3p구유항유선암천이약물개발적잠질。
Objective:To analyze the inhibiting mechanism of microRNA-199a/b-3p ( miR-199a/b-3p) on cell motility of breast cancer cells.Methods:The expression of PAK4 in MDA-MB-231 cells transfected with miR-199a/b-3p was detected by Western blot.The biology behaviors of MDA-MB-231 cells transfected with miR-199a/b-3p or PAK4 SiRNA were analysed by cell migration assay,invasion assay and protrusion dynamics.Results: MiR-199a/b-3p could suppress the expression of PAK 4 in MDA-MB-231 cells.Comparing with normal control ,miR-199a/b-3p or PAK4 SiRNA could suppress the migration ,invasion and membrane protrusion of MDA-MB-231 cells.Conclusion:miR-199a/b-3p could suppress the expression of PAK4,which are considered key breast cancer suppressors and inhibit the cell motility of breast cancer cells.