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《Heparanase对肝癌细胞生物学行为的影响-论文.pdf》由会员上传分享,免费在线阅读,更多相关内容在应用文档-天天文库。
1、第23卷第29期China中Jo国ur现na代lo医fM学od杂er志nMedicineVoI.23No.292013年1O月0ct.2013文章编号:1005—8982(2013)29—0036—05·论著·Heparanase对肝癌细胞生物学行为的影响梁天成,付文广,雷正明(1.四川省泸州市中医医院外一科,四川泸州646000;2.泸州医学院附属医院肝胆胰外科,四川泸州646000)摘要:目的探讨乙酰肝素酶(Heparanase)对肝癌细胞生物学功能的影响。方法利用荧光定量PCR检测人肝癌细胞HepG2、Huh一7、Bel一7402、MHCC一97H以及SMMC一7
2、721中Heparanase的表达水平;设计及合成3条Heparanase特异性小分子干扰RNA(siRNA)并用于转染Heparanase表达高的一株人肝癌细胞,通过荧光定量PCR和Westernblotting检验干扰效率;MTT法检测细胞增殖能力;Transwell小室法检测细胞的侵袭能力;ArmexinV/PI染色法检测细胞凋亡。结果MHCC一97H细胞中的Heparanase表达水平显著高于其余4株肝癌细胞(P<0.05);siRNA3能瞬时下调肝癌细胞的Heparanase水平;siRNA介导的Heparanase基因沉默使肝癌细胞的增殖速度放慢,侵袭能力减
3、弱,凋亡率升高,差异具有统计学意义(P4、ouTraditionalChineseMedicineHospital,Luzhou,Sichuan64600,P.R.China;2.DepartmentofHepatobiliarySurgery,theAffiliatedHospital,LuzhouMedicalCollege,Luzhou,Siehuan646000,P.R.China)Abstract:【Objective】Todeterminewhethersilencingofheparanaseexpressioncanabolishthemalig—nantcharacteristicsofhep5、atocellularcarcinomacells.【Methods】Heparanaseexpressionlevelsoffivehepato—cellularcarcinomacelllinesweremeasuredbyreal-timePCR.Threeheparanase—specificsmallinterferingRNA(siRNAs)weredesigned,synthesized,andtransfeetedintoculturedhepatocellularcarcinomacelllineMHCC-97H.Heparanaseexpressio6、nwasmeasuredbyreal-timequantitativePCRandwesternblotting.CellproliferationwasdetectedbyMTFcolorimetry.Theinvitrocellinvasionwasdetectedbymatrigelinvasionas—say.Thecellapoptoticratewasanalyzedbyusingflowcytometry.【Results】TransfectionofsiRNAresultedinreducedexpressionofheparanase.ThesiRNA7、-mediatedsilencingofheparanasesuppressedthecellularproliferationandinvasionofhepatocellularcarcinomacells.Inaddition,cellapoptosisratesweresignificantlyincreasedafterknock—downofheparanase.【Conclusion】Theseresultsdemonstratedthatgenesilencingofheparanasecaneficientlyaboli
4、ouTraditionalChineseMedicineHospital,Luzhou,Sichuan64600,P.R.China;2.DepartmentofHepatobiliarySurgery,theAffiliatedHospital,LuzhouMedicalCollege,Luzhou,Siehuan646000,P.R.China)Abstract:【Objective】Todeterminewhethersilencingofheparanaseexpressioncanabolishthemalig—nantcharacteristicsofhep
5、atocellularcarcinomacells.【Methods】Heparanaseexpressionlevelsoffivehepato—cellularcarcinomacelllinesweremeasuredbyreal-timePCR.Threeheparanase—specificsmallinterferingRNA(siRNAs)weredesigned,synthesized,andtransfeetedintoculturedhepatocellularcarcinomacelllineMHCC-97H.Heparanaseexpressio
6、nwasmeasuredbyreal-timequantitativePCRandwesternblotting.CellproliferationwasdetectedbyMTFcolorimetry.Theinvitrocellinvasionwasdetectedbymatrigelinvasionas—say.Thecellapoptoticratewasanalyzedbyusingflowcytometry.【Results】TransfectionofsiRNAresultedinreducedexpressionofheparanase.ThesiRNA
7、-mediatedsilencingofheparanasesuppressedthecellularproliferationandinvasionofhepatocellularcarcinomacells.Inaddition,cellapoptosisratesweresignificantlyincreasedafterknock—downofheparanase.【Conclusion】Theseresultsdemonstratedthatgenesilencingofheparanasecaneficientlyaboli
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