首页|MicroRNA-505调控PLK1对前列腺癌细胞恶性生物学行为的影响及机制研究

MicroRNA-505调控PLK1对前列腺癌细胞恶性生物学行为的影响及机制研究

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目的 探讨miR-505通过调控Polo样激酶1(PLK1)表达对前列腺癌PC-3细胞增殖、迁移和侵袭的影响.方法 取第4代对数生长期PC-3细胞,随机分为对照组、NC组、miR-505 inhibitor组、mimic NC组和miR-505 mimic组,除对照组外,其余各组细胞分别转染in-hibitor NC、miR-505 inhibitor、mimic NC 和 miR-505 mimic,48 h 后,分别采用 qRT-PCR 检测细胞中miR-505的表达量、MTT法检测细胞存活率、划痕实验检测细胞的迁移能力、Transwell实验检测细胞的侵袭能力、双荧光素酶报告基因检测miR-505与PLK1的靶向关系、蛋白印迹法检测PLK1、波形蛋白、神经钙黏蛋白(N-cad)和上皮钙黏蛋白(E-cad)的相对表达量.结果 与对照组比较,miR-505 inhibitor组的miR-505表达量和E-cad蛋白相对表达量降低,细胞存活率、细胞迁移率以及PLK1、波形蛋白和N-cad蛋白相对表达量升高,细胞侵袭能力增强(均P<0.05);与对照组比较,miR-505 mimic组的miR-505表达量和E-cad蛋白相对表达量升高,细胞存活率、细胞迁移率以及PLK1、波形蛋白和N-cad蛋白相对表达量降低,细胞侵袭能力减弱(均P<0.05);与NC组比较,miR-505 inhibitor组的miR-505表达量和E-cad蛋白相对表达量降低,细胞存活率、细胞迁移率以及PLK1、波形蛋白和N-cad蛋白相对表达量升高,细胞侵袭能力增强(均P<0.05);与miR-505 inhibitor组比较,miR-505 mimic组的miR-505表达量和E-cad蛋白相对表达量升高,细胞存活率、细胞迁移率以及PLK1、波形蛋白和N-cad蛋白相对表达量降低,细胞侵袭能力减弱(均P<0.05);与mimic NC组比较,miR-505 mimic组的miR-505表达量和E-cad蛋白相对表达量升高,细胞存活率、细胞迁移率以及PLK1、波形蛋白和N-cad蛋白相对表达量降低,细胞侵袭能力减弱(均P<0.05).结论 miR-505可减弱前列腺癌细胞的增殖、迁移和侵袭能力,其机制可能是通过抑制PLK1的表达发挥作用.
Effects of microRNA-505 on malignant biological behavior of prostate cancer cells by regulating PLK1 and its mechanism
Objective To investigate the effects of miR-505 on the proliferation,migration and invasion of prostate cancer PC-3 cells by regulating the expression of Polo-like kinase 1(PLK1).Methods PC-3 cells in the fourth generation of logarithmic growth phase were randomly divided into control group,NC group,miR-505 inhibitor group,mimic NC group and miR-505 mimic group.Ex-cept the control group,cells in the other groups were transfected with inhibitor NC,miR-505 inhibitor,mimic NC and miR-505 mimic,respectively.The control group was not treated.After 48 h,qRT-PCR was used to detect the expression of miR-505,MTT assay was used to detect cell survival rate,scratch assay was used to detect cell migration ability,Transwell assay was used to detect cell invasion ability,dual luciferase reporter gene was used to detect the targeting relationship between miR-505 and PLK1,and western blot was used to detect the relative expression levels of PLK1,Vimentin,neurocadherin(N-cad)and epithelial cadherin(E-cad)proteins.Results Compared with the control group,the relative expression of miR-505 and E-cad protein were decreased in miR-505 inhibitor group,while cell survival rate,cell migration rate,and the relative expression of PLK1,Vimentin and N-cad pro-tein were increased,and the cell invasion ability was enhanced(all P<0.05).The relative expres-sion of miR-505 and E-cad protein increased in miR-505 mimic group,while cell survival rate,cell migration rate,the relative expression of PLK1,Vimentin and N-cad protein decreased(all P<0.05).Compared with NC group,the relative expression of miR-505 and E-cad protein in miR-505 inhibitor group were decreased,while cell survival rate,cell migration rate,the relative expression of PLK1,Vimentin and N-cad protein in miR-505 inhibitor group were increased,and the cell invasion ability was enhanced(all P<0.05).Compared with miR-505 inhibitor group,the relative expression of miR-505 and E-cad protein in miR-505 mimic group increased,while cell survival rate,cell migra-tion rate,the relative expression of PLK1,Vimentin and N-cad protein in miR-505 mimic group de-creased,the cell invasion ability was decreased(all P<0.05).Compared with NC mimic group,the relative expression of miR-505 and E-cad protein in miR-505 mimic group increased,while cell surviv-al rate,cell migration rate,the relative expression of PLK1,Vimentin and N-cad protein in miR-505 mimic group decreased(all P<0.05).Conclusions miR-505 attenuates the proliferation,migration and invasion of prostate cancer cells,possibly by inhibiting the expression of PLK1.

Prostatic NeoplasmsPolo Like Kinase 1miR-505Cell ProliferationCell Move-ment

年智、穆元忠、申大年、李国权

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青海省第五人民医院泌尿外科,西宁 810000

青海省第五人民医院肿瘤科,西宁 810000

前列腺肿瘤 Polo样激酶1 miR-505 细胞增殖 细胞运动

2017年青海省卫生计生系统科研课题

2017-wjzd-05

2024

国际泌尿系统杂志
中华医学会,湖南省医学会

国际泌尿系统杂志

CSTPCD
影响因子:0.414
ISSN:1673-4416
年,卷(期):2024.44(5)