SCI结果写作技巧Word下载.docx
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SCI结果写作技巧Word下载.docx
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8.EffectsofONOO-oncellviabilityinFaDucells
9.CurcumininhibitscellviabilityofFaDucells
10.MEK1inhibitionsuppressesERK1/2activationandinhibitsmyelomacellproliferation
11.CurcumininhibitsthemigrationandinvasionabilityofFaDucells
12.TargetedNOX4knockdownwithaspecificsiRNAblocksRMF-EGstimulusonMCF-7migration
13.EGFR-MSCdemonstratedenhancedmigratoryresponsestowardtumor-conditionedmedia,whichwaspartiallydependentonEGFandEGFR
14.EffectsofcurcuminonmRNAexpressionsofmetastasis-relatedgenesinFaDucells
15.EffectsofONOO-onmRNAexpressionofPDCD4inFaDucells
16.DownregulationofTbRIIinnon-small-celllungcancers(NSCLC)
17.KLF8PromotesCellProliferationandInvasion,InhibitsApoptosis,andInducesEMTInVitro
18.
二、结果开头句
评估….效果,运用….方法,在…..药物浓度以及在….时间作用于….细胞
1.Inordertoassessthecytotoxiceffectofcurcuminonthehumanhypopharyngealcancercells,FaDucellswereculturedwithcurcuminatfinalconcentrationsof10,20,40,60,80,and100µ
Mfor24h,48h,and72h,then,MTTassaywascarriedoutrespectively.
2.MorphologicalchangesofFaDucellswereexaminedbyacridineorangecytochemistrystainingat48haftertreatmentwithcurcuminat0,20,40,60,and80µ
M,respectively.
3.TheFaDucellcycledistributionwasanalyzedbyMultiCyclesoftwaretoinvestigatetheeffectofcurcuminonthecellcycle.
4.Theanti-metastaticactivityofcurcuminwasevaluatedusingtheTranswellassay.
5.Western-blotanalyseswereperformedtoestimatethelevelsofcaspase-9,caspase-3,Bcl-2andBaxinFaDucellsinresponsetocurcumin(Fig.5A).
6.AscurcumininhibitedFaDucellsmigrationandinvasion,wefurtherinvestigateditseffectonthemetastasis-relatedgenes.
7.SGNswereexposedtoONOO(100mM)for24hwithorwithoutcurcuminpretreatment.
8.Todelineate描绘thesignalingpathwayofmitochondria-relatedapoptosis,weinvestigatedtheeffectofONOOontheactivationofApaf-1,Caspase-9andCaspase-3geneswhichareinvolvedinthemitochondrion-dependentapoptosispathway.
9.FlowcytometryassaywithAnnexinV/PIdoublestainingshowedthattheapoptoticrateincreasedto50.273.26%aftertreatingwith100mMONOOfor24h(Fig.4B)
10.ToexaminetheroleofZnf179inthecellcycleduringneuronaldifferentiation,P19cellswereinfectedwithnegativecontrolandZnf179shRNAviruses.
11.WeevaluatedcellcycleparametersafterPD98059modulationinfourcases:
threecaseshadhighERKactivity,onecasewasERKnegative.
12.TostudythepossibleroleofNOX4intheRMF-EG-mediatedstimulusonMCF-7migration,weusedatargetedknockdownbysiRNAapproachtodownregulatetheenzymeexpression.
13.InordertotestourhypothesisthatEGFRtransfectionenhancesmigrationofMSCstowardtumorcells,weemployedinvitrotwo-chambermigrationassays.First,wetestedmigratoryresponsesofprimaryMSCsandEGFR-MSCtowardGL261-orB16-conditionedmedia(Fig2a).
14.RT-PCRanalysesofthemRNAlevelsofPDCD4wereperformedtoestimatetheeffectofONOO-ontheexpressionofPDCD4gene(Fig.4A).
15.ToverifywhetherTbRIIlevelisdownregulatedinhumanlungtumours,weanalysedforTbRIIexpressionbyRT-PCRusingRNAsamplesfrom46lungtumourspecimens(20squamouscellcarcinoma,19adenocarcinoma,andsevenlargecellcarcinoma)(Figure1A).
16.SinceweobservedreducedTbRIImRNAexpressioninNSCLC,wetestedtheexpressionofTbRIIproteininlysatesmadefromtumourspecimensbyWesternblotanalysis.
17.The1DCa2mRNAlevelduringheartdevelopmentwascarriedoutbyreal-timeRT-PCRusingtotalRNAisolatedfromfetal,neonatal,4-to6-wk-old,and6-to8-mo-oldratatrialtissueusing18SrRNAasaninternalcontrol.
18.ToinvestigatetheeffectofKLF8inEMT,theexpressionofEMTmarkerswereassessed.
19.Astelomeraseactivityisfrequentlyproposedtobeassociatedwiththemalignantphenotype,weattemptedtodeterminewhetheracorrelationexistsbetweenionizingradiation-inducedcelldeathandtelomeraseactivity.
20.goodCellscollectedatdifferenttimespostirradiationwereexaminedforcellviabilityandtelomeraseactivity.
21.Sincecellsinanactivelygrowingtumoraredistributedindifferentcyclestages,wealsoattemptedtodeterminewhetherthetelomeraseactivityinexponentiallygrowingcellsisaffectedbyionizingradiation.WefirstevaluatedcellcyclephasedistributionsingrowingHeLacellsbyflowcytometry.
22.InviewofthecorrelationbetweentheexpressionstatusofhTERTandtelomeraseactivity
三、结果表达:
1.主系表结构:
结果做主语
主语——thetrend,theproportions,thepercentages,thelevels,theexpressions,cellviability,therate,theactivity,
系表/谓语——1)wassignificantlyobserved,
2)升高increasedto50.273.26%,weregraduallyincreased,wereincreasedsignificantly,wassignificantlyhigher,wasamplifiedinglomeruli,
3)降低werereduced,werereducedto73.41±
5.84%,wasdecreasedobviously,wasmarkedlyreducedto,wereunabletogenerateamigratorystimulusonMCF-7cells,
程度副词——用于有显著性统计学差异的词significantly,markedly,remarkably;
用于形态学表现有差异的词obviously,apparently;
其他gradually逐渐地;
mildly轻微地,greatly,appreciably可感觉到地;
1)AsshowninFigure1,atrendofdecreasingviabilitywithincreasingcurcuminconcentrationandexpendingtreatment-timewassignificantlyobservedinFaDucells,indicatingthatcurcumininhibitedthecellviabilityinadose-andtime-dependentmanner.
2)FaDucellsweretreatedwith0,20,and40µ
Mcurcuminfor48hrespectively,asshowninFigure3,theproportionsofFaDucellsinSphaseweregraduallyincreased(from14.23±
2.17%to23.10±
2.33%,35.13±
3.35%),meanwhile,thepercentagesofcellsatG0/G1phaseweregraduallydecreased(from67.03±
3.37%to57.87±
4.60%,46.10±
2.98%,).
3)Thelevelsofmigrationwerereducedto73.41±
5.84%and58.54±
7.76%ofthecontrol(freshmediumalone)levelat10and20µ
Mcurcumin,respectively(Fig.4A,C).
4)Theproteinexpressionsofcleavedcaspase-9(37kDa),cleavedcaspase-3(17kDa)andBaxwereincreasedsignificantlyinFaDucellstreatedwithcurcumin20µ
Mand40µ
Mcomparedtothatofcontrol(Fig.5B),while,theexpressionofBcl-2genewasdecreasedobviously(Fig.5B),aswellasthedecreaseofratioofBcl-2/Bax(datanotshown).
5)mRNAexpressionlevelsofpro-metastasisgenesMMP-2andMMP-9werereduced,whereas,Ecadherin,ananti-metastasisgene,wasincreasedsignificantlybycurcuminatconcentrationsof10µ
Mand20µ
M,respectively(Fig.6)
6)Cellviabilitywasmarkedlyreducedtoapproximately59.573.02%afterexposureto100mMONOOfor24hcomparedwiththecontrolgroup(Fig.2A,B).
7)FlowcytometryassaywithAnnexinV/PIdoublestainingshowedthattheapoptoticrateincreasedto50.273.26%aftertreatingwith100mMONOOfor24h(Fig.4B),while,theratesofcontrolgroupandcurcumin-pretreatedgroupwere4.361.47%and7.310.99%respectively(Fig.4A,C).StatisticanalysesrevealedthattheapoptoticratewassignificantlyhigherinONOOgroupcomparedwiththatincontrolgroup(Fig.4D,p0.001),andthattheapoptoticrateinthecurcumin-pretreatedgroupdeclinedremarkablyincomparisonwiththatinONOOgroup(Fig.4D,p0.001).
8)TheSODactivityoftheONOO-treatedgroupwas36.783.62%ofthecontrolgroup.InSGNspretreatedwithcurcumin(15mM,12h),thelevelofSODactivitywas86.193.13%ofcontrolgroup.
9)ThemRNAexpressionofApaf-1,Caspase-9,Caspase-3wasincreasedsignificantlyafterexposuretoONOO100mMfor24hasevidencedbyRT-PCR(Fig.7).Moreover,themRNAexpressionofanti-apoptoticgeneBcl-2wasdecreasedwhiletheBaxgeneexpressionwasincreased.
10)AsFigure3Ashows,RMF-EGcellstransientlytransfectedwithsiNOX4wereunabletogenerateamigratorystimulusonMCF-7cells.
11)TheTbRIIexpressionwasfoundtobedecreasedin80%ofsquamouscellcarcinoma,42%adenocarcinoma,and72%largecellcarcinoma
12)ThePCRproductforHip1wasamplifiedinglomeruli,whereasnoexpressionwasdetectedintherestofthekidneylackingglomeruli(Figure1).
13)ThereactionintensityoftheimmunocytochemistrywasinaccordancewithqRTPCRandWesternblotanalyses
14)Weexamined2hallmarksofEMT:
E-cadherinwasdown-regulated,andVimentinwasup-regulatedinHCCcelllineswithhighKLF8-expressionbyqRT-PCRanalysis.
15)Down-regulationofmesenchymalmarkers(N-cadherin,vimentin,andfibronectin)andupregulationoftheepithelialmarker(E-cadherin)wereobservedbyRT-PCRafterKLF8siRNA(Figure2F).
16)GoodThesurvivalofdifferentcelltypesafterexposuretogradeddosesofradiation(137Cesiumgammaraysat1.1Gy/min)asdeterminedbyclonogenicassayisshowninFig.1.
17)GoodAstrongcorrelationwasdetectedbetweentelomeraseactivityandcellviabilityinHeLacellstreatedwithionizingradiation.
18)GoodAsimilarpatternofdecreaseintelomeraseactivity(Fig.6)andcellviability(datanotshown)withanincreaseinradiationdosetreatmentwasobservedinthecolorectalcarcinoma(RKO)cellline.
19)Telomeraseactivityisdetectableinmosthumantumortissueandintumor-derivedcelllines,butnotinnormalcellsadjacenttotumorsormixedwithtumor-derivedcelllines(29).
20)
2.主谓宾结构:
药物做主语
主语——药物名称curcumin,treatment,pr
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