双氢青蒿素对人卵巢癌细胞株ho-8910凋亡作用的实验分析-experimental analysis of dihydroartemisinin on apoptosis of human ovarian cancer cell line ho - 8910.docxVIP

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双氢青蒿素对人卵巢癌细胞株ho-8910凋亡作用的实验分析-experimental analysis of dihydroartemisinin on apoptosis of human ovarian cancer cell line ho - 8910.docx

双氢青蒿素对人卵巢癌细胞株ho-8910凋亡作用的实验分析-experimental analysis of dihydroartemisinin on apoptosis of human ovarian cancer cell line ho - 8910

双氢青蒿素对人卵巢癌细胞株HO-8910凋亡作用的实验研究摘要目的:探讨双氢青蒿素(DHA)对人卵巢癌细胞株H0-8910裸鼠皮下移植瘤的生长及Bcl-2表达的影响,并对其机制作初步探讨。方法:将人卵巢癌细胞株H0-8910注入裸鼠的腋下,建立人卵巢癌移植瘤的动物模型,并随机将建模成功的30只裸鼠分为5组,即DHA低剂量组(100mg/kg)、DHA中剂量组(150mg/kg)、DHA高剂量组(200mg/kg),阳性对照组(顺铂2mg/kg)、空白组(生理盐水),6只/组。顺铂采取腹腔注射的方式给药,5d后停药,其余各组均采用灌胃给药法持续给药10d,第11d处死裸鼠,称取瘤质量,比较干预后各组移植瘤抑瘤率;应用RT-PCR法测定移植瘤中Bcl-2mRNA的表达;免疫组化法和western-blot法检测肿瘤细胞内Bcl-2蛋白的表达。结果:①病理学观察见细胞的体积较大,胞质疏松,核深染,可有不同程度的核固缩、核碎裂及核溶解,细胞中可见局灶性坏死。②DHA对裸鼠移植瘤的生长有一定的抑制作用,并具有浓度依赖性,DHA低、中、高剂量组及顺铂组的抑瘤率分别为25.4%、36.9%、44.3%及55.7%,与生理盐水组比较差异均有统计学意义P0.05,DHA各实验组抑瘤率与顺铂组相比,差异有统计学意义P0.05。③RT-PCR法检测到双氢青蒿素组Bcl-2基因表达下调。④免疫组化及western-blot法结果证实双氢青蒿素组Bcl-2蛋白表达明显低于空白组P0.05,且随着DHA剂量的增加Bcl-2蛋白表达减弱。结论:双氢青蒿素对人卵巢癌裸鼠皮下移植瘤的生长有明显的抑制作用,且与剂量有一定的关系,其机制可能与下调Bcl-2的表达诱导细胞凋亡有关。关键词:双氢青蒿素;Bcl-2;卵巢癌;裸鼠;InhibitoryeffectsofdihodryartemisininonovariancancerHO-8910cellObjectiveToexploretheeffectofdihodryartemisinin(DHA)onthegrowthofhumanovariancancerHO-8910cellsandtheactivityofBcl-2,andstudythemechanism.MethodsNudemousemodeloftransplantedovariancancerwasestablishedbyinjectingHO-8910cellsintoaxillaryfossa,andthenthemicewererandomlydividedintolow-dose-groupofDHA,middle-dose-groupofDHA,high-dose-groupofDHA,positivecontrolDDPgroup,blankcontrolgroup,eachofwhichwascomposedofsixnudemice.ThoseinDDPcontrolgroupintraperitonealinjectedwithDDPatadosageof2mg/kgbodyweightandreceivedfor5days.ThemiceinDHA-low-dose、DHA-middledoseandDHA-high-dosegroupsweregavagewithDHAatdosagesof100、150and200mg/kgbodyweighteveryotherdayrespectively,andwhilethoseinblankcontrolgroupgavagewithsaline,andcontinuouslyreceivedfor10daysinnudemice.Killthemiceonday11aftertreatmenttoobservethetumorgrowthandcomparisonoftumorinhibitoryrateaftertheintervention.DeterminationofBcl-2expressionintransplantedtumorbyRT-PCR,andtheexpressionofBcl-2wasdeterminedbyimmuno-histo-chemicalassayandwestern-blot.Results①Pathologicalobservationshowscellsbecomelarge,andloosecytoplasm,nucleusdeeplystained,pyknosis,nucleardissolution,nuclearfragmentation,chromatinlumpsalsocanbefound,andcellshave

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