期刊文献+

渥曼青霉素对人胃癌细胞的作用及机制 被引量:2

The effect and mechanism of wortmannin on human gastric carcinoma cells
原文传递
导出
摘要 目的探讨渥曼青霉素(wortmannin)对人胃癌细胞的作用及机制。方法采用10,30,60nmol/L的AKT抑制剂wortmannin,以不同时间对胃癌细胞SGC7901进行干预;并设对照组运用MTT法检测细胞的增殖抑制情况;用Westernblot检测NF-κB核蛋白表达水平;RT-PCR检测NF-κB基因的转录水平。结果3种浓度的wortmannin都对胃癌SGC7901细胞的生长均具有抑制作用,其抑制效应呈明显剂量和时间依赖性(P<0.01或P<0.05);而对照组未见明显变化(P>0.05)。随着wortmannin作用时间的延长,NF-κBmRNA及核蛋白的表达水平均显著低于对照组(P<0.05)。结论wort-mannin可抑制胃癌SGC7901细胞的生长;可能通过胃癌中存在的AKT/NF-κB信号通路调节NF-κB的表达而发挥作用。 Objective To explore the effect and mechanism of wortmannin on the human gastric carcinoma cells. Methods SGC7901 cells were treated with 10nmol/L,30nmol/L and 60nmol/L of wortmannin, a specific inhibitor of AKT, for different time periods. Cell viability was estimated by MTT assay. Western blot was used to detect the level of NF-κB neucleoprotein and reverse transcriptasepolymerase chain reaction ( RT-PCR ) was used to determine transcription of NF-κB mRNA. Results All three different concentrations of wortmannin could inhibit the growth of SGC7901 ceils, and the depression effect obviously depended on time and drug dose( P 〈 0.01 and P 〈 0.05 ). However, the cell viability was no change in the control group ( P 〉 0. 05 ). As the action time of wortmannin was prolonged, neucleoprotein and mRNA expression of NF-κB significantly decreased compared with the control ( P 〈 0.05 ). Conclusions The findings suggest that wortmannin can inhibit the growth of gastric carcinoma SGC7901 cells, and the action may depend on an AKT/NF-κB pathway in gastric carcinoma cells.
作者 秦龙 张才全
出处 《中国普通外科杂志》 CAS CSCD 北大核心 2009年第10期1035-1038,共4页 China Journal of General Surgery
关键词 胃肿瘤 NF-ΚB 渥曼青霉素 蛋白激酶B Stomach Neoplasms NF- κB Wortmannin Protein Kinase B
  • 相关文献

参考文献12

  • 1刘映辉,所剑,李寿柏,刘航.β-catenin和核因子-κB表达与胃癌的相关性研究[J].中国老年学杂志,2007,27(20):1987-1989. 被引量:3
  • 2Guillermet-Guibert J, Saint-Lanrent N, Davenne L, et al. Novel synergistic mechanism for sst2 somatostatin and TNFalpha receptors to induce apoptosis: crosstalk between NF-kappaB and JNK pathways[J]. Cell Death Differentiation, 2007 , 14 (2) :197 -208.
  • 3Choi, IN - Kwon, IAee JS, et al. Streptochlorin, a marine natural product, inhibits NF-kappaB activation and suppresses angiogenesis in vitro [ J ]. Microbiol Biotechnol, 2007, 17 (8) :1338 - 1343.
  • 4Starenki DV, Namba H, Saenko VA, et al. Induction of thyroid cancer cell apoptosis by a novel NF-κB inhibitor dehydroxymethylepoxyquinomiein [ J ] . Clin Cancer Res, 2004, 10(20) :6821 -6829.
  • 5Sharma C, Kaur J, Shishodia S, et al. Curcumin down regulates smokeless tobacco-induced NF-kappaB activation and COX-2 expression in human oral premalignant and cancer cells[ J]. Toxicology,2006,228 ( 1 ) : 1 - 15.
  • 6Sinha-Datta U, Horikawa I, Michishita E, et al. Transcriptional activation of hT-ERT through the NF-kappaB pathway in HTLV-I-transformed cells [ J ] . Blood, 2004 , 104 ( 8 ) : 2523 -2531.
  • 7苗丽君,王静.Akt与肿瘤的研究进展[J].国外医学(生理病理科学与临床分册),2004,24(5):406-409. 被引量:38
  • 8Ruhul Abid, Shaodong Guo, Takashi Minami, et al. Vascular endothelial growth factor activates PI3 K/Akt/Forkhead signaling in endothelial ceils [ J ]. Arterioscler Thromb Vasc Biol, 2004,24(2) :294 -300.
  • 9Thoompson JE , Thompson CB. Putting the Rap on Akt [ J ] . Clin Oncolo ,2004,22 (20) :4217 - 4226.
  • 10Coffey JC, Wang JH, Smith MJF, et al. Phosphoinositide 3- Kinase accelerates postoperative tumor growth by inhibiting apotosis and enhancing resistance to chemotherapyinduced apotosis [ J ]. J Biol Chem, 2005, 280 (22) : 20968 - 20977.

二级参考文献34

  • 1Cantley LC.The phosphoinositide 3-kinase pathway[J].Sci-ence,2002,296(5573):1655-1657.
  • 2Burgering BM,Kops GJ.Cell cycle and death control:long live Forkheads[J].Biochem Sci,2002,27(7):352-360.
  • 3Poh TW,Pervaiz S.LY294002 and LY303511 sensitize tumor cells to drug-induced apoptosis via intracellular hydrogen pero-xide production independent of the phosphoinositide 3-kinase-Akt pathway[J].Cancer Res,2005,65(14):6264-6274.
  • 4Nicholson KM,Anderson NG.The protein kinase B/Akt signal-ling pathway in human malignancy[J].Cell Signal,2002,14(5):381-395.
  • 5Potter C J, Pedraza LG, Xu T. Akt regulates growth by directly phosphorylating Tsc2 [ J ]. Nat Cell Biol, 2002,4 (9) :658-665.
  • 6Vander Heiden MG, Plas DR, Rathmell JC, et al . Growth factors can influence cell growth and survival through effects on glucose metabolism[J]. Mol Cell Biol, 2001 ,21 (17) :5899-5912.
  • 7Edinger AL, Thompson CB. Akt maintains cell size and survival by increasing mTOR-dependent nutrient uptake [ J ]. Mol Biol Cell,2002 , 13 (7) : 2276-2288.
  • 8West KA, Brognard J, Clark AS, et al. Rapid Akt activation by nicotine and a tobacco carcinogen modulates the phenotype of normal human airway epithelial cells [ J]. J Clin Invest, 2003,111(1) :81-90.
  • 9Nam SY, Jung GA, Hur GC, et al. Upregulation of FLIP(S) by Akt, a possible inhibition mechanism of TRAIL-induced apoptosis in human gastric cancers [ J ]. Cancer Sci, 2003,94 ( 12 ) : 1066-1073.
  • 10Gagnon V, St-Germain ME, Parent S, et al. Akt activity in endometrial cancer cells: regulation of cell survival through cIAP-1 [ J].Int J Oncol, 2003 ,23(3) :803-810.

共引文献41

同被引文献14

引证文献2

二级引证文献7

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