miR-424-3p靶向SMAD7调控子宫内膜癌 增殖、侵袭机制研究

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[中图分类号]R173 [文献标识码]A [文章编号]1673—5293(2026)02—0016-09
Study on mechanism of miR-424-3p targeting SMAD7 in regulating proliferationandinvasionofendometrialcarcinoma
CUI Jinghong1,CHEN Yang²,ZHANG Chaoxia1
(1.Department of obstetrics,Changde Hospital,Xiangya School of Medicine,Central South University eFirstPeople'sHospitalofChangdeCity),HunanChangde415Ooo,China;2.TheEmergencyDepartment
The22th hospital ofChinesepeople's liberationarmyhospital,Qinghai Golmud816Oo,China)
[Abstract]ObjectiveToinvestigate whethermiR-424-3pregulates the proliferationandinvasionof endometrialcarcinoma(EC)by mediatingSMAD7,andtoexploretheregulatorymechanism.Methods Predictivebinding siteanalysisandgeneexpresion assessment wereconductedusing TargetScan dataand the GEPIA database.Cellproliferation,migration,andinvasion were evaluated through EdUstaining,wound healing,andTranswellassays.Theregulatoryefectsof miR-424-3pandSMADonECwere evaluated invivothrough tumortransplantation experiments.Results Validationconfirmedthebinding sitebetweenmiR-424-3p andSMAD7.KnockoutofmiR-424-3psignificantlyinhibitedtheinvasionandproliferationofHEC-1AandRL95-2cels,while promotingcellapoptosis.However,sh-SMAD7reversed theefectsofmiR-424-3ponthesecells.Additionall,sh-SMAD7could significantlyounteracttheefectsofmiR-424-3pihbtorsontheexpressionofepithelialmesenchyaltransition(EMrelated proteinsinHEC-1AandRL95-2cellines.mR-424-3pinhibitorscouldsignificantlyinhibit thegrowthoftransplantedtumorsbut sh-SMAD7couldreversetheefectsofmiR-424-3pinhibitors.ConclusinmiR-424-3pregulates theproliferation,invasion,nd epithelialmesenchymal transition process of HEC-1AandRL95-2celsby modulating SMAD7,suggesting that miR-424-3p/ SMAD7 may be a new target for the prevention and treatment of endometrial carcinoma.
[Key words] miR-424-3p;endometrial carcinoma;SMAD7;epithelial-mesenchymal transition;proliferation;invasion
在全球,子宫内膜癌(endometrialcarcinoma,EC)的患病率呈上升趋势,尤其是在发达国家[1-2]根据世界卫生组织(WorldHealth Organization,WHO)统计,子宫内膜癌是全球女性生殖系统癌症中患病率最高的疾病之一[3]。(剩余11226字)