首页|环状RNA_PLEKHM3通过miR-320/KLF4轴调控宫颈癌细胞上皮间质转化

环状RNA_PLEKHM3通过miR-320/KLF4轴调控宫颈癌细胞上皮间质转化

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目的 探讨环状RNA含普列克底物蛋白同源域的家族M3 成员(PLEKHM3)(circRNA_PLEKHM3)通过调控微小RNA-320(miR-320)/畸变样因子 4(KLF4)轴在宫颈癌细胞上皮间质转化(EMT)行为中的作用与机制.方法 采用实时定量PCR(qRT-PCR)法检测宫颈癌细胞Hela和CaSki中circRNA_PLEKHM3 的表达水平;RNA 荧光原位杂交检测circRNA_PLEKHM3 在人宫颈癌上皮细胞 CaSki中的定位;双荧光素酶报告基因实验检测 circRNA_PLEKHM3 和 miR-320 的靶向关系,以及miR-320 和KLF4 的靶向关系;对CaS-ki细胞过表达circRNA_PLEKHM3;另外设置三组,分别为在过表达 circRNA_PLEKHM3 的基础上过表达 miR-320、沉默KLF4,以及在过表达 miR-320 的基础上沉默 KLF4.qRT-PCR检测 CaSki 中 miR-320 的表达水平;Western blot 检测CaSki细胞中KLF4 和EMT标志物上皮钙黏蛋白(E-cadher-in)、神经钙黏蛋白(N-cadherin)、波形蛋白(Vimentin)、基质金属蛋白酶(MMP)-2 和MMP-9 的表达;Transwell实验检测细胞迁移数和侵袭细胞数.结果 circRNA_PLEKHM3 在Hela和CaSki中的表达均降低(P<0.05),其主要定位在细胞质中;双荧光素酶报告基因实验显示miR-320 和circRNA_PLEKHM3 存在靶向关系,KLF4 和 miR-320 存在靶向关系;过表达circRNA_PLEKHM3 抑制miR-320 和N-cadherin、Vim-entin、MMP-2、MMP-9 的蛋白表达,上调E-cadherin的蛋白表达,减少细胞迁移和侵袭数(P<0.05);在过表达circRNA_PLEKHM3 的基础上过表达miR-320 或沉默KLF4 均能够促进miR-320 和N-cadherin、Vimentin、MMP-2、MMP-9 蛋白的表达,上调E-cadherin蛋白的表达,减少迁移和侵袭细胞数(P<0.05);然而在过表达miR-320 的基础上沉默KLF4,KLF4和N-cadherin、Vimentin、MMP-2、MMP-9 蛋白的表达受到抑制,E-cadherin蛋白的表达上调,细胞迁移和侵袭数减少(P<0.05).结论 circRNA_PLEKHM3 过表达可能通过 miR-320/KLF4 轴调控宫颈癌细胞的EMT.
CircRNA_PLEKHM3 regulates epithelial mesenchymal transformation of cervical cancer cells through the miR-320/KLF4 axis
Objective To investigate the role and mechanism of circular RNA containing pleckstrin homology do-main of Pleckstrin homology domain family M member 3(circRNA_PLEKHM3)in regulating epithelial-mesenchy-mal transition(EMT)behavior in cervical cancer cells through the miR-320 and KLF4.Methods The expression levels of circRNA_PLEKHM3 in cervical cancer cells Hela and CaSki were detected by real-time quantitative PCR(qRT-PCR).RNA fluorescence in situ hybridization was used to determine the localization of circRNA_PLEKHM3 in human cervical cancer epithelial cells CaSki.Dual luciferase reporter gene experiments were conducted to inves-tigate the targeting relationship between circRNA_PLEKHM3 and miR-320,as well as the targeting relationship be-tween miR-320 and KLF4.CaSki cells were overexpressed with circRNA_PLEKHM3.Additionally,three groups were set up:overexpression of miR-320 on the basis of circRNA_PLEKHM3 overexpression,silencing of KLF4 on the basis of circRNA_PLEKHM3 overexpression,and silencing of KLF4 on the basis of miR-320 overexpression.qRT-PCR was performed to detect the expression levels of miR-320 in CaSki.Western blot experiments were con-ducted to determine the expression of KLF4 and EMT markers including E-cadherin,N-cadherin,Vimentin,MMP-2,and MMP-9 in CaSki cells.Transwell assays were performed to measure cell migration and invasion.Results The expression of circRNA_PLEKHM3 decreased in Hela and CaSki cells(P<0.05),mainly localized in the cy-toplasm.The dual luciferase reporter gene experiment demonstrated a targeting relationship between miR-320 and circRNA_PLEKHM3,as well as between KLF4 and miR-320.Overexpression of circRNA_PLEKHM3 inhibited the protein expression of miR-320,N-cadherin,Vimentin,MMP-2,and MMP-9,up-regulated the protein expression of E-cadherin,and reduced cell migration and invasion(P<0.05).Overexpression of miR-320 or silencing of KLF4 on the basis of circRNA_PLEKHM3 overexpression both promoted the protein expression of miR-320,N-cad-herin,Vimentin,MMP-2,and MMP-9,down-regulated the protein expression of E-cadherin,and increased cell migration and invasion(P<0.05).However,silencing of KLF4 on the basis of miR-320 overexpression inhibited the protein expression of KLF4,N-cadherin,Vimentin,MMP-2,and MMP-9,up-regulated the protein expression of E-cadherin,and reduced cell migration and invasion(P<0.05).Conclusion Overexpression of circRNA_PLEKHM3 regulates EMT in cervical cancer cells through the miR-320/KLF4 axis.

circular RNA_PLEKHM3miRNA-320krüppel-like factor 4cervical cancer cellsepithelial-mes-enchymal transitionmigrationinvasion

张亚男、崔莹、王天娇、杜忠蕾

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牡丹江医学院附属红旗医院妇产科妇科病区,牡丹江 157000

cirRNA_PLEKHM3 miRNA-320 畸变样因子4 宫颈癌细胞 上皮间质转化 迁移 侵袭

黑龙江省卫生健康委科研项目

2020-408

2024

安徽医科大学学报
安徽医科大学

安徽医科大学学报

CSTPCD北大核心
影响因子:1.095
ISSN:1000-1492
年,卷(期):2024.59(3)
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