hrgerbb信号系统与22rv1前列腺癌细胞增殖关系研究-study on the relationship between hrg erbb signal system and proliferation of 22rv 1 prostate cancer cells.docx
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hrgerbb信号系统与22rv1前列腺癌细胞增殖关系研究-study on the relationship between hrg erbb signal system and proliferation of 22rv 1 prostate cancer cells
中文摘要HRG/ErbB信号系统与22RV1前列腺癌细胞增殖关系研究目的:探讨HRG/ErbB信号系统对激素非依赖性前列腺癌细胞株22RV1增殖的影响及其作用机制。方法:首先,应用共聚焦显微镜和流式细胞仪技术对22RV1前列腺癌细胞HER-2和HER-3的表达进行定性和定量的检测;其次,应用MTT法明确HRG对22RV1前列腺癌细胞增殖的影响;最后,结合流式细胞仪周期检测及蛋白印记技术明确HRG/ErbB信号系统影响22RV1前列腺癌细胞增殖的具体作用机制。结果:1、共聚焦显微镜技术证实FITC标记的HER2和PE标记的HER3在前列腺癌细胞株22RV1都有低度表达。2、FITC-HER2表达率﹦(6.4800±2.39729)%,PE-HER3表达率﹦(4.6200±1.33492)%,表明HER2、HER3在22RV1前列腺癌细胞均低表达。3、MTT实验表明HRGβ1能促进22RV1细胞增殖。4、HRGβ1激活22RV1前列腺癌细胞PI3K/AKT信号通路,p-AKT的表达显著升高。5、随着HRGβ1干预时间的延长,S期细胞比例逐渐升高,G0/G1期细胞比例逐渐降低。6、随着HRGβ1干预时间的延长,cyclinD1表达量随之增加。结合流式细胞仪检测的细胞周期改变,HRGβ1可能通过诱导cyclinD1表达升高从而促进G0/G1期向S期转换。7、HRGβ1通过降解IκB快速活化NF-κB通路。结论:HRG/ErbB信号系统促进22RV1前列腺癌细胞增殖,其机制涉及PI3K/AKT通路活化和cyclinD1的表达升高,同时伴有NF-κB通路的激活。关键词:HRG/ErbB信号系统,激素非依赖性前列腺癌,22RV1细胞株,PI3K/AKT通路,细胞周期,NF-κB1ABSTRACTROLEOFHRG/ErbBSIGNALSYSTEMINTHEPROLIFERATIONOF22RV1PROSTATECANCERCELLLINEObjective:Investigatingthemechanismofprolilferationof22RV1cellinductedbythesignalofHRG/ErbBsystem.Methods:First,detectingtheexpressionofHER-2andHER-3bytheconfocalmicroscopyandflowcytometry;Secend,usingthemethordsofMTTassaytoexaminingtheinfluenceofHRGon22RV1cellprolilferation;Third,usingthetechnologyofflowcytometryandwesternblottoinvestigatethemechanismofprolilferationof22RV1cellinductedbytheHRG/ErbBsignalsystem.Results:1.TheFITCconjugatedHER2andPEconjugatedHER3arelowlevelespressedon22RV1cells.2.FITC-HER2%﹦(6.4800±2.39729)%,PE-HER3%﹦(4.6200±1.33492)%.3.HRGβ1promtotetheproliferationprocessof22RV1cells.4.HRGβ1activatthepasswayofPI3K/AKT.5.UndertheinterfereofHRGβ1,thecellPercentageofSphasebecomeincreasedfollowedbythedecreaseofG0/G1phasescellPercentage.6.WiththeprolongoftheHRGβ1intervention,italsohappenstheincreasingresultofcyclinD1expression.7.HRGβ1canactiveNF-κBpasswayinaquicklymanner.Conclusion:TheHRG/ErbBsignalsystemcanpromtotetheproliferationprocessof22RV1prostatecancercells,themechanisminvolvesinisactivatingofthePI3K/AKTpasswayandtheincreasingexpressionofcyclinD1alsowiththeactivatingofNF-κBpassway.KeyWords:HRG/ErbBsignalsystem,AndrogenIndependentProstateC
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