首页出版说明中文期刊中文图书环宇英文官网付款页面

microRNA-345在恶性胸膜间皮瘤细胞中的异常表达及其靶基因生物信息学分析

黄 何菲, 李 君贤, 彭 理, 范 岩鑫, 张 芳芳, 朱 丽瑾
杭州医学院公共卫生学院

摘要


目的:探究microRNA-345(miR-345)在恶性胸膜间皮瘤细胞中的异常表达,并利用生物信息学对其靶基因进行筛选及分析。方法利用荧光定量PCR(qPCR)对恶性胸膜间皮瘤细胞(NCI-H2452、MSTO-211H、NCI-H2052)和正常间皮细胞MeT-5A细胞中miRNA-345表达水平进行检测分析,通过生物信息学分析预测miRNA-345下游基因,利用metascape分析miRNA-345下游基因的通路。结果三株恶性间皮瘤细胞相比MeT-5A细胞miRNA-345的表达量均降低,生物信息学分析筛选出了26个miRNA-345下游基因(上调9个,下调17个),通过富集分析发现筛选出的miRNA-345下游基因主要参与脉管系统发育、细胞连接组织、上皮细胞迁移、Ras蛋白信号转导、细胞外基质组织和上皮细胞分化等信号通路。结论miRNA-345在恶性胸膜间皮瘤细胞中表达量下降,生物信息学分析结果提示脉管系统发育、细胞连接组织、上皮细胞迁移、Ras蛋白信号转导、细胞外基质组织和上皮细胞分化等相关通路参与了miRNA-345在恶性胸膜间皮瘤细胞中的表达调控。

关键词


恶性胸膜间皮瘤细胞;miRNA-345;生物信息学分析

全文:

PDF


参考


[1]ReidG,JohnsonTG,vanZandwijkN.ManipulatingmicroRNAsfortheTreatmentofMalignantPleuralMesothelioma:Past,PresentandFuture.FrontOncol.2020.10:105.[2]TolaniB,AcevedoLA,HoangNT,HeB.HeterogeneousContributingFactorsinMPMDiseaseDevelopmentandProgression:BiologicalAdvancesandClinicalImplications.IntJMolSci.2018.19(1).[3]LoRussoG,TessariA,CapeceM,etal.MicroRNAsfortheDiagnosisandManagementofMalignantPleuralMesothelioma:ALiteratureReview.FrontOncol.2018.8:650.[4]LeeYS,DuttaA.MicroRNAsincancer.AnnuRevPathol.2009.4:199-227.[5]杨琴,王杰,吕沐瀚,唐世孝.miR-345抑制人胰腺癌细胞的增殖能力研究.现代医药卫生.2018.34(06):828-832.[6]雷永华,王磊,赵致广,张伟,付晓亮.miR-345靶向调控TGM1抑制膀胱癌的初步研究.现代生物医学进展.2018.18(18):3412-3419.[7]ShenZ,WangX,YuX,ZhangY,QinL.MMP16promotestumormetastasisandindicatespoorprognosisinhepatocellularcarcinoma.Oncotarget.2017.8(42):72197-72204.[8]SunJZ,ZhangJH,LiJB,etal.MXRA5IsaNovelImmune-RelatedBiomarkerThatPredictsPoorPrognosisinGlioma.DisMarkers.2021.2021:6680883[9]KimGJ,RheeH,YooJE,etal.IncreasedexpressionofCCN2,epithelialmembraneantigen,andfibroblastactivationproteininhepatocellularcarcinomawithfibrousstromashowingaggressivebehavior.PLoSOne.2014.9(8):e105094.[10]WengY,FanX,BaiY,etal.SLC2A5promoteslungadenocarcinomacellgrowthandmetastasisbyenhancingfructoseutilization.CellDeathDiscov.2018.4:38.[11]VicenteCM,LimaMA,NaderHB,TomaL.SULF2overexpressionpositivelyregulatestumorigenicityofhumanprostatecancercells.JExpClinCancerRes.2015.34(1):25.[12]ShaoQ,ZhangZ,CaoR,ZangH,PeiW,SunT.CPA4PromotesEMTinPancreaticCancerviaStimulatingPI3K-AKT-mTORSignaling.OncoTargetsTher.2020.13:8567-8580.[13]GuQ,LuoY,ChenC,JiangD,HuangQ,WangX.GREM1overexpressioninhibitsproliferation,migrationandangiogenesisofosteosarcoma.ExpCellRes.2019.384(1):111619.[14]LiuCH,HuRH,HuangMJ,etal.C1GALT1promotesinvasivephenotypesofhepatocellularcarcinomacellsbymodulatingintegrinβ1glycosylationandactivity.PLoSOne.2014.9(8):e94995.[15]FraileJM,Campos-IglesiasD,RodríguezF,EspañolY,FreijeJM.ThedeubiquitinaseUSP54isoverexpressedincolorectalcancerstemcellsandpromotesintestinaltumorigenesis.Oncotarget.2016.7(46):74427-74434.[16]LingJ,ZhangL,ChangA,etal.OverexpressionofKITLGpredictsunfavorableclinicaloutcomesandpromoteslymphnodemetastasisviatheJAK/STATpathwayinnasopharyngealcarcinoma.LabInvest.2022.102(11):1257-1267.[17]WengX,ChenW,HuW,etal.PTPRBpromotesmetastasisofcolorectalcarcinomaviainducingepithelial-mesenchymaltransition.CellDeathDis.2019.10(5):352.[18]LiangM,YaoW,ShiB,etal.CircularRNAhsa_circ_0110389promotesgastriccancerprogressionthroughupregulatingSORT1viaspongingmiR-127-5pandmiR-136-5p.CellDeathDis.2021.12(7):639.[19]MaX,ChenH,LiL,YangF,WuC,TaoK.CircGSK3BpromotesRORAexpressionandsuppressesgastriccancerprogressionthroughthepreventionofEZH2trans-inhibition.JExpClinCancerRes.2021.40(1):330.[20]KimYJ,JungYD,KimTO,KimHS.Alu-relatedtranscriptofTJP2geneasamarkerforcolorectalcancer.Gene.2013.524(2):268-74.[21]王黎.RNA结合蛋白QKI通过转录后调节COX2抑制胃癌的发生发展.见:卢兹凡,杨栋,主编.(02),2012.[22]WuY,XuM,HeR,XuK,MaY.ARHGAP6regulatestheproliferation,migrationandinvasionoflungcancercells.OncolRep.2019.41(4):2281-2888.[23]ChoWC,JangJE,KimKH,YooBC,KuJL.SORBS1servesametastaticroleviasuppressionofAHNAKincolorectalcancercelllines.IntJOncol.2020.56(5):1140-1151.




DOI: http://dx.doi.org/10.12361/2705-0459-05-03-125272

Refbacks

  • 当前没有refback。