氟哌啶醇与新型人重组肿瘤坏死因子逆转肿瘤细胞耐药机制的研究.pdfVIP

  • 2
  • 0
  • 约14.26万字
  • 约 98页
  • 2019-06-09 发布于江苏
  • 举报

氟哌啶醇与新型人重组肿瘤坏死因子逆转肿瘤细胞耐药机制的研究.pdf

氟哌啶醇和新型人重组肿瘤坏死因子逆转肿瘤耐药机理的研究 5 e}圭em。冁e秘py e攫毫ct flfo黻clin量c越existi端d那gs,壤e糟v粥al agai建s耄獭u{蛀帆g cellline K562/Dox resistance(MDR)in eryt王lr01eukemic Doxorubicin(Dox)-resistant andbroastcancercelllineMcF一7/Dox rhTNF—NC andits byhaloperidol(Hal)and mech黼is撼珊festu程斑T沁fev瞒蠢e蔻etsof泗R ZYY一6 exl凇t by臻o fr。m herbsand Chinese new LY一980503Were compound also synmetic investigated. te舰zoliurn LDH e骶ctsof dye assay,血ecytotoxic various Using assay(MTT)and eonee辩露a《o珏s at0.20 eells of蚤ox nmO{忍法强562摩oxa聪MCF.?辫oxwe糟stu鑫i《, ofMDRrelated MDR MDRl, associated Expression genes protein(MRP), glutathion—s—tmsferasePi(GSTH)and K562/Doxcells垤eated TbpoII氆of by 12.5umol,LHai rhTNF-NC500—50∞ reverSe Or 彬mlwefe ass8yedby chain now transcriptaSe—polymerasereaction(RT—PCR).Using c”ometry(FcM), i芏ltracellularDox O、6。25、12.5and25 8cc媾mul砒io鞋镰K562囝ox

文档评论(0)

1亿VIP精品文档

相关文档