OALib Journal期刊
ISSN: 2333-9721
费用:99美元
|
|
|
毛兰素诱导结肠癌sw480细胞凋亡的分子机制
DOI: 10.3724/SP.J.1145.2011.00512, PP. 512-516
Keywords: 毛兰素,人结肠癌细胞sw480,细胞增殖,细胞凋亡,细胞周期,石斛,中药
Abstract:
毛兰素是名贵中药材石斛的活性化合物之一,研究了其对人结肠癌sw480细胞的增殖抑制作用及其诱导的细胞凋亡分子机制.实验表明,毛兰素能显著抑制结肠癌sw480细胞的增殖,且随着药物浓度与时间增加,抑制率呈明显的剂量时间效应,48h半数抑制浓度ic50为24.5nmol/l;毛兰素能显著诱导结肠癌sw480细胞凋亡,并诱导细胞周期阻滞于g2-m期;分子机制研究显示,毛兰素通过下调xiap、bcl-xl蛋白表达以及激活caspase-9、caspase-7、caspase-3和parp活性从而诱导sw480细胞凋亡.结果表明毛兰素可能对结肠癌的防治具有潜在药用价值.图6参17
References
[1] | 7gongyq,yifan,leiliu,wudz,changzl,wangzt.erianininducesajnk/sapk-dependentmetabolicinhibitioninhumanumbilicalveinendothelialcells.invivo,2004,18(2):223~228
|
[2] | 8hongw(洪卫),masl(马胜林),dulb(杜灵彬),fengjg(冯建国),lingyt(凌雨田),mouhz(牟瀚周),guoy(郭勇).experimentalstudyoferianininducingingastriccarcinoma.chinacancer(中国肿瘤),2008,17(6):499~501
|
[3] | 10tangy,simoneauar,liaowx,yig,hopec,liuf,lis,xiej,holcomberf,jurnakfa,mercolad,hoangbh,zix.wif1,awntpathwayinhibitor,regulatesskp2andc-mycexpressionleadingtog1arrestandgrowthinhibitionofhumaninvasiveurinarybladdercancercells.molcancerther,2009,8(2):458~468
|
[4] | 15jiangx,wangx.cytochromec-mediatedapoptosis.annurevbiochem,2004,73:87~106
|
[5] | 16kashkarh.x-linkedinhibitorofapoptosis:achemoresistancefactororahollowpromise.clincancerres,2010,16(18):4496~4502
|
[6] | 17connollyk,mitterr,muirm,jodrelld,guichards.stablexiapknockdownclonesofhct116coloncancercellsaremoresensitivetotrail,taxanesandirradiationinvitro.cancerchemotherpharmacol,2009,64(2):307~316
|
[7] | 1labiancar,merellib.screeninganddiagnosisforcolorectalcancer:presentandfuture.tumori,2010,96(6):889~901
|
[8] | 2tsaoas,kimes,hongwk.chemopreventionofcancer.cacancerjclin,2004,54(3):150~180
|
[9] | 3dingxy(丁小余),zhangwm(张卫明),wangzt(王峥涛),xuls(徐珞珊).summarizationofthestudiesoftaxonomyandpharmacognosyofethnologicalmaterialsofdendrobium.chinacadmedmagorg(中国医学生物技术应用杂志),2003,8(1):1~14
|
[10] | 4chenxm(陈晓梅),guosx(郭顺星).advancesintheresearchofconstituentsandpharmacologyofdendrobium.natprodres&dev(天然产物研究与开发),2001,13(1):70~75
|
[11] | 5liym,wangh,liugq.erianininducesapoptosisinhumanleukemiahl-60cells.actapharmacolsin,2001,22(11):1018~1022
|
[12] | 6gongyq,fany,wudz,yangh,huzb,wangzt.invivoandinvitroevaluationoferianin,anovelanti-angiogenicagent.eurjcancer,2004,1(41):1554~1565
|
[13] | 9tangy,simoneauar,xiej,shahandehb,zix.effectsofthekavachalconeflavokawainadifferinbladdercancercellswithwild-typeversusmutantp53.cancerprevres,2008,1(6):439~451
|
[14] | 11tangy,lix,liuz,simoneauar,xiej,zix.flavokawainb,akavachalcone,exhibitsrobustapoptoticmechanismsonandrogenreceptor-negative,hormone-refractoryprostatecancercelllinesandreducestumorgrowthinapreclinicalmodel.internjcancer,2010,127(8):1758~1768
|
[15] | 12yeeds,tangy,lix,liuz,guoy,ghaffars,mcqueenp,atreyad,xiej,simoneauar,hoangbh,zix.thewntinhibitoryfactor1restorationinprostatecancercellswasassociatedwithreducedtumorgrowth,decreasedcapacityofcellmigrationandinvasionandareversalofepithelialtomesenchymaltransition.molcancer,2010,9(1):162
|
[16] | 13tangy,parmakhtiarb,simoneauar,xiej,fruehaufj,lillym,zix.lycopeneenhancesdocetaxel’seffectincastration-resistantprostatecancerassociatedwithinsulin-likegrowthfactorireceptorlevels.neoplasia,2011,13(2):108~119
|
[17] | 14gaoyr(高雅蓉),anjx(安君霞),zhuqy(朱启�),lif(李甫),macy(马超英),wangmk(王明奎),tangyx(唐亚雄).inhibitoryeffectofraddeaninainhumannon-smallcelllungcancerh460cells.chinjapplenvironbiol(应用与环境生物学报),2010,12(5):637~641
|
Full-Text
|
|
Contact Us
service@oalib.com QQ:3279437679 
WhatsApp +8615387084133
|
|