简介:死亡联系域的蛋白质Daxx施加包括调停的许多报导功能经由激活c6月N终端从FasL发信号到apoptosisapoptosis的kinase(JNK),正式就职和抑制,和染色质改变的规定。它原来从酵母被克隆用船边交货对相似物体之连续感觉而形成心像口的细胞内部的尾巴的二混血儿的屏幕诱饵。而许多起始的报告仍然保持争论,Daxx在一系列压力信号包括UVirradiation,过氧化氢治疗和TGF-β治疗触发的apoptosis的规定起重要作用,是清楚的。在这评论,我们在Axinbeing上集中连接Daxx到p53的一个拴住的因素。
简介:Cisplatindamagescochlearhaircellsandspiralganglionneuronsthroughcelldeathsignalingpathwaysthatarenotfullyunderstood.Weusedfocusedapoptosisgenemicroarraystostudyearlychangesingeneexpres-sionincochlearculturesfromP3neonatalratstreatedwithcisplatin(0.2mM).After12hoursofcisplatintreat-ment,morethan50%ofthe96genesonthearrayshowedasignificantdecreaseinexpression,consistentwithwidespreadcelldeath.However,after3hoursofcisplatintreatment,10genesshowedsignificantincreaseinex-pressionintotalcochleartissue.Inexperimentswithsubsetsofcochleartissues,at3h,cisplatininducedincreasedexpressionof12genesinthecochlearsensoryepithelium(basilarmembrane)and11genesinthespiralganglion(tissueofRosenthal'scanal,containingthespiralganglion).Theseincludedpro-andanti-apoptoticgenesin-volvedinthep53signalingpathway,TNFreceptorfamily,NF-kappaBpathway,deathdomainfamily,deatheffec-tordomainfamily,Bcl-2family,CARDfamily,TRAFfamily,andGTPsignaltransduction.Althoughthechangesingeneexpressionshowedanoverlapbetweenbasilarmembraneandspiralganglion,otherchanges,whichmayreflecttheuniqueresponseofeachtissue,werealsoobserved.Pifithrin-αblockedcisplatin-inducedup-regulationofgenesinthep53signalingpathwaywhenassayedbybothsuperarrayandrealtimePCR.Thedataaddtoourunderstandingoftheinvolvementofp53incisplatin-inducedototoxicityandotoprotection,conferredbythep53inhibitorPifithrin-α.
简介:TherearetwopossibleoutcomeswhenDNAdamageoccursinnormalmammaliancells:eitherinductionofcell-cyclecheckpointwhichinhibitstheprogressofthecellcyclesaswellasactivatesDNArepairpathways,oractivationofapoptosistoeliminatedamagedcells.Thep53tumour-suppressorgeneplaysakeyroleinselectingthesepathways.Inourpresentworks,thehumangastriccancercelllineAGSwastreatedwithtripchlorolide,apotentantitumorcompoundpurifiedfromaChineseherbTripterygiumWilfordiiHook.Singlecellgelelectrophoresis(Cometassay)showedthatthetreatmentoftripchlorolideresultedinDNAdamageinAGScells.ThedamagedAGScellswentthroughapoptosis,whichwastime-anddose-dependent.
简介:摘要目的探讨血清及胸水P53抗体水平检测对肺癌诊断价值和临床意义。方法采用酶联免疫吸附法(ELISA)检测36例肺癌患者、29例经手术或化疗治疗后的肺癌患者血清P53抗体,并以30例健康体检者作对照,其中15例肺癌患者同时检测胸水P53抗体,以16例良性胸水作为对照。结果肺癌组血清P53抗体水平为3.879±5.963IU/ml,明显高于对照组0.144±0.019IU/ml,且差异有高度显著性(P<0.01),阳性率为52.8%;在肺癌治疗组,血清P53抗体水平为1.86±2.914IU/ml,阳性率为34.5%,而且与对照组和未治疗肺癌组差异无显著性(P>0.05);肺癌胸水P53抗体水平18.95±7.319IU/ml高于良性胸水对照组0.267±0.318IU/ml,且具有高度显著性差异(P<0.01),阳性率86.7%。结论检测血清及胸水P53抗体水平有助于肺部良恶性疾病的诊断及鉴别诊断,血清P53抗体可成为肺癌的血清标志物,胸水P53抗体检测比血清更具敏感性。
简介:摘要p53基因是一种常见的抑癌基因,它几乎参与了人类所有肿瘤的生物学过程。骨肉瘤是一种最常见的骨原发恶性肿瘤,p53基因改变是骨肉瘤发生发展过程中的一个重要事件,并影响着化疗效果和预后。现就p53基因在骨肉瘤中的研究做一综述。
简介:Recentstudiesindicatethatcell-cyclecheckpointsaretightlycorrelatedwiththeregulationofapoptosis,inwhichp53playsanimportantrole.OurpresentworksshowthattheexpressionofE6/E7oncogenesofhumanpapillomavirusinHeLacellsisinhibitedinthepresenceofanti-tumorreagenttripchlorolide(TC),whichresultsintheup-regulationofp53inHeLacells.Interestingly,underthesameTC-treatment,thecellsattheearlyS-phasearemoresusceptibletoapoptosisthanthoseatthemiddleS-phasealthoughp53proteinisstabilizedtothesamelevelinbothsituations.Significantdifferenceisexhibitedbetweenthetwospecifiedexpressionprofiles.Furtheranalysisdemonstratesthatanti-apoptoticgenesurvivinisup-regulatedbyp53intheTC-treatedmiddle-Scells,whereasitisdown-regulatedbyp53intheTC-treatedearly-Scells.Takentogether,thepresentstudyindicatesthatthedifferentialp53-regulatedexpressionofsurvivinatdifferentstagesofthecellcycleresultsindifferentcellularoutputsunderthesameapoptosis-inducer.
简介:Toevaluatetheeffectofadenovirus-mediatedp53gene(Adp53)onapoptosisandradiosensitivityofhumangastriccarcinomacelllines.Methods:Recombinantadenovirusexpressingwild-typep53lineswithdifferentp53geneticstatus.p53proteinexpressionwasdetectedbyimmunohistochemistryassayandwesternblotassay.Cellsurvivalwasassessedusingaclonogenicassay.TUNELassaywasusedindeterminationofapoptosis.FourhumangastriccarcinomacellsinfectedwithAdp53wereirradiatedwith4GyandcellcycledistributionandSub-G1peakwereassayedbyflowcytometry.Results:G2/Marrest,apoptosisandinhibitionoftumorcellproliferationwereinducedbyinfectionatAdp53at100MOIwhichcausedhightransferrateofwild-typep53andstrongexpressionofp53proteininfourhumangastriccarcinomacells.Theradio-enhancementratioofAdp53at4Gywere3.0forWcell,3.6forMcell,2.2forneocelland2.5for823cellinvitro.Conclusion:ThisstudydemonstratedthatAdp53transferincreasedcellularapoptosisandradiosensitivityofhumangastriccarcinomacelllinesinvitroindependentlyoncellularintrinsicp53statusthussupportingthecombinationofp53genetherapywithradiotherapyinclinicaltrials.
简介:Abstract:Thisstudyinvestigatedtherelationshipbetweenhumanpapillomavirus(HPV)genotypeandexpressionofp53andp21^WAH1.Expressionofp53andp21^WAH1in35casesofcondylomaacuminatumspecimensinfectedbyHPV6/llandHPV16/18werestudiedusingimmunohistochemicalstaining.Allspecimensofthecondylomaacuminatumcasewerepositiveforexpressionofp53andp21^WAH1.Theexpressionofp53incondylomaacuminatuminfectedbyHPV16/18wassignificantlylowerthanthatinspecimensinfectedbyHPV6/ll.However,expressionofp21wAHbetweenthetwogroupswasnotsignificantlydifferent.Expressionofp53incondylomaacuminatumislikelyrelatedtoHPVgenotype,expressionofp21^WAH1wasnotrelatedtoHPVgenotype.
简介:目的探讨p27^kipl、p53蛋白在胃癌中的表达关系和预后意义。方法用免疫组化法同步检测20例胃良性病变标本及80例胃癌组织中pZ7、p53的表达。结果80例胃癌中p27蛋白阳性率为41,25%(33/80),低于胃良性病变标本100%(20/20),p53阳性率在胃癌中为43.75%(35/80),而在胃良性病变标本中为0。胃癌p27阳性组的p53阳性率为66.67%,显著高于p27阴性组(P<0.05),p27与p53呈正相关,p27与预后弱相关,p53与预后密切相关。结论p27、p53相互作用,对胃癌发生发展起重要作用;p27表达愈强,p53表达愈弱,说明预后较好,反之则差,联合检测pZ7、p53可辅助胃癌诊断,估计预后,选择治疗方案。
简介:Objective:Toinvestigatethepost-transcriptionalregulationofp21WAF1/CIP1byp53.Methods:TheMDA-MB-468cellshaveendogenousmutantp53andtheMCF7cellslineshavewtp53.Recombinantp53expressionandp21WAF1/CIP1inductionweredetectedbyWesternblotanalysis.Northernblotanalysiswascarriedouttoexaminewhetherchangesinp21WAF1/CIP1proteinlevelsinMCF7cellstreatedwithAdCMVp53arereflectedatthemRNAlevel.FlowcytometricanalysisofMCF7cellsfollowingoverexpressionofrecombination.Results:Theratioofp53:p21WAF1/CIP1wasbelow1attheearlystagesofAdCMVp53infection,butincreasedto1.6byday3andto9.7byday5post-infection.Asexpected,p21WAF1/CIP1expressionwasnotdetectableinMDA-MB-468cellsdespitethepresenceofhighlevelsofmutantp53protein.TheG1/SratiosinuntreatedcontrolsandAdCMVβgalinfectedMCF7cellswere1.10and1.35,respectively.ByNorthernblotanalyzingthep21WAF1/CIP1:GAPDHratiosatdifferenttimepointsagainsttheratioattimepoint0,amaximum3-foldinductionofp21WAF1/CIP1mRNAexpressionrelativetountreatedcontrolwasobservedonday1post-infection.TheflowcytometricanalysisindicatedthatMCF7cellsinfectedwithAdCMVp53undergoG1arrestatbothtimepointsstudied,withG1/Sratiosrangingfrom5.54atday1to5.65atday7.TheG1/SratiosinuntreatedcontrolsandAdCMVβgalinfectedMCF7cellswere1.10and1.35,respectively.Conclusion:Thisstudydemonstratedthatp53couldregulatep21WAF1/CIP1geneexpressionatboththetranscriptionalandpost-transcriptionallevelsinMCF7cells.Thelattermechanismmaybeinvolvedinorberesponsiblefor,theinductionofcellcyclearrestbytranscription-defectivemutantsofp53.