期刊文献+

LY294002对SGC7901/VCR细胞VCR耐药逆转作用研究

Drug resistance reversing effects on gastric carcinoma cell line by inhibition of PI3K/PKB signal pathway and its mechanism
下载PDF
导出
摘要 目的观察LY294002对SGC7901/VCR胃癌细胞长春新碱(VCR)耐药的逆转作用,并探讨其可能机制。方法通过MTT法明确LY294002可以逆转SGC7901/VCR对VCR的耐药作用后,采用TUNEL检测细胞的凋亡,高效液相法检测细胞内药物浓度,RT-PCR法和Western blot法分别检测细胞中MDR1、caspase-3和XIAP的基因和蛋白表达水平。结果 LY294002能明显提高VCR的诱导细胞凋亡作用,明显增加细胞内VCR的浓度,并可降低耐药细胞中MDR1、XIAP的基因和升高caspase-3表达水平。结论抑制PI3K/PKB通路可逆转胃癌耐药,其机制可能与降低耐药基因MDR1的表达以及调控凋亡相关基因caspase-3和XIAP的表达有关。 Objective To observe whether inhibition of PI3K/AKT signal pathway could reverse drug resistance of gastric carcinoma,and to study its potential mechanism.Methods The growth inhibition effects of VCR alone and VCR in combination with PI3K/PKB inhibitor LY294002 on SGC7901/VCR cells were detected by in vivo and in vitro experiments.The protein and mRNA expression levels of MDR1,caspase-3 and XIAP in SGC7901/VCR cells were determined by Western-blot and reverse transcription PCR.The content of VCR in cells was determined with high performance liquid chromatography(HPLC).Besides,the apoptosis was detected by TUNEL.Results LY294002 enhanced the sensitivities of SGC7901/VCR cells to VCR significantly,and promoted the apoptosis rate induced by VCR prominently.The protein and gene expression levels of MDR1 and XIAP were inhibited,while the expression of caspase-3 was improved significantly.When VCR coupled with the LY294002,the VCR accumulation in cells increased significantly than used only.Conclusion Inhibition of PI3K/PKB signal pathway by LY294002 can reverse the drug resistance of gastric carcinoma cell line.Reduction of MDR1 expression levels,and regulation of apoptosis related genes,such as caspase-3 and XIAP expression levels play key roles in this progress.
出处 《重庆医学》 CAS CSCD 北大核心 2010年第21期2875-2877,F0002,共4页 Chongqing medicine
关键词 LY294002 SGC7901/VCR细胞 凋亡 MDR1 LY294002 SGC7901/VCR cells apoptosis MDR1
  • 相关文献

参考文献12

  • 1Zhang D,Fan D.Multidrug resistance in gastric cancer:recent research advances and ongoing therapeutic challenges[J].Expert Rev Anticancer Ther,2007,7(10):1369.
  • 2Barancik M,Bohacova V,Sedlak J,et al.LY294002,a specific inhibitor of PI3K/Akt kinase pathway,antagonizes P-glycoprotein-mediated multidrug resistance[J].Eur J Pharm Sci,2006,29(5):426.
  • 3Han Z,Hong L,Han Y,et al.Phospho Akt mediates multidrug resistance of gastric cancer cells through regulation of P-gp,Bcl-2 and Bax[J].J Exp Clin Cancer Res,2007,26(2):261.
  • 4Vlahos CJ,Matter WF,Hui KY,et al.A specific inhibitor of phosphatidylinositol 3-kinase,2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002)[J].J Biol Chem,1994,269(7):5241.
  • 5夏曙,于世英.抑制PI3K/Akt信号转导通路提高化疗效果的实验研究[J].肿瘤,2006,26(4):311-313. 被引量:21
  • 6Parkin DM,Bray F,Ferlay J,et al.Global cancer statistics,2002[J].CA Cancer J Clin,2005,55(2):74.
  • 7Hohenberger P,Gretschel S.Gastric cancer[J].Lancet,2003,362(9380):305.
  • 8Breier A,Barancik M,Sulova Z,et al.P-glycoprotein--implications of metabolism of neoplastic cells and cancer therapy[J].Curr Cancer Drug Targets,2005,5(6):457.
  • 9Nicholson KM,Quinn DM,Kellett GL,et al.LY294002,an inhibitor of phosphatidylinositol-3-kinase,causes preferential induction of apoptosis in human multidrug resistant cells[J].Cancer Lett,2003,190(1):31.
  • 10Ghosh S,Karin M.Missing pieces in the NF-kappaB puzzle[J].Cell,2002,109 Suppl:S81.

二级参考文献19

  • 1Yuan JY, Yankner BA. Apoptosis in the nervous system [ J]. Nature,2000,407 : 802 - 9.
  • 2Bergin AM, Connolly M. New antiepileptic drug therapies [ J ].Neurol Clin ,2002,20(4) : 1163 - 82.
  • 3Ohmori H, Oura H, Yasuda Met al. Developmental neurotoxicity of phenytoin on granule ceils and Purkinje cells in mouse cerebellum [ J ]. J Neurochem, 1999,72 (4) : 1497 - 506.
  • 4Yan GM, Irwin RP, Lin SZ et al. Diphenylhydantoin induces apoptotic cell death of cultured rat cerebellar granule neurons[ J ]. J Pharmacol Exp Ther, 1995,274 ( 2 ) : 983 - 90.
  • 5Ferrari G, Minozzi MC, Zanellato AM et al. GM1, like IGF-I and GDNF, prevents neuronal apoptosis[ J ]. Ann N Y Acad Sci, 1998,845:408.
  • 6Kenchappa P, Yadav A, Singh G et al. Rescue of TNFalpha-inhibited neuronal ceils by IGF-1 involves Akt and c-Jun N-terminal kinases [ J ]. J Neurosci Res, 2004,76 ( 4 ) :466 - 74.
  • 7Often D, Shtaif B, Hadad D et al. Protective effect of insulin-like-growth-factor-1 against dopamine-induced neurotoxicity in human and rodent neuronal cultures: possible implications for Parkinson's disease [ J ]. Neurosci Lett, 2001,316 ( 3 ) : 129 - 32.
  • 8Zheng WH, Kar S, Dore S, Quirion R. Insulin-like growth factor-1 (IGF-1) :a neuroprotective trophic factor acting via the Akt kinase pathway[J]. J Neural Transm Suppl,2000, (60) :261 -72.
  • 9Guang-Mei Yan, Steven M Paul. Cultured cerebellar granule neurons as a model of neuronal apoptosis [ M]//In Apoptosis Techniques and Protocols. ( Ed : Judes Poirier) humana Press. Inc Totowa NJ 07512, USA ,49 - 66.
  • 10Dudek HSR, Datta TF, Franke MJ et al. Regulation of neuronal survival by the serine-threonine protein kinase Akt [J]. Science,1997,275:661 - 5.

共引文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部