期刊文献+

奥曲肽对SGC-7901胃癌细胞中Fas,FasL及P53表达的影响 被引量:5

Effects of octreotide on expression of Fas, FasL and P53 in human gastric cancer SGC-7901 cells
下载PDF
导出
摘要 目的:探讨奥曲肽(OCT)对胃癌细胞SGC-7901中Fas,FasL,P53,P21,P27和c-Myc表达的影响.方法:流式细胞术和RT-PCR法分别用于检测经OCT(1×10-7mol/L)处理前后胃癌细胞SGC-7901中Fas,FasL,P53,P21,P27,c-Myc阳性癌百分率、mRNA表达和蛋白表达及细胞周期G0/G1、S、G2/M的变化.结果:胃癌细胞SGC-7901经OCT诱导6、12、24和48h后,Fas和FasL mRNA表达均明显增加,P53mRNA表达则显著减少,而P21,P27和c-Myc mRNA表达均无明显变化;胃癌细胞SGC-7901经OCT诱导12h后,Fas和FasL蛋白相对表达强度也显著增加,P53蛋白相对表达强度则明显降低(5.5±0.3vs3.2±0.1,5.1±0.3vs4.5±0.1,3.3±0.2vs4.9±0.3,P<0.05或0.01),而P21,P27和c-Myc蛋白相对表达强度均无明显改变.细胞周期G0/G1、S、G2/M在OCT处理前后的变化并不明显.结论:OCT能上调SGC-7901胃癌细胞中Fas和FasL表达,下调突变型p53表达,是其诱导凋亡作用的重要机制之一. AIM: To investigate whether OCT affects the expression of Fas, FasL, P53, P21, P27 and c-Myc in SGC-7901 HGC cells.METHODS: Expression percentage of Fas, FasL, P53, P21, P27, c-Myc-positive cells and G0/G1, S, G2/M stage were detected by using flow cy- tometry (FCM) with or without OCT treatment. Reverse transcription-polymerase chain reaction (RT-PCR) and FCM in SGC-7901 HGC cells were applied to evaluate the mRNA and protein expression levels of Fas, FasL, P53, P21, P27 and c-Myc in SGC-7901 HGC cells treated with and without OCT.RESULTS: After treatment with 1 x 10.7 mol/L OCT for 6, 12, 24, 48 h, although P53 mRNA expression was significantly decreased, Fas and FasL mRNA expression were both significantly increased in SGC-7901 HGC cells. However, P21, P27 and c-Myc mRNA expression did not significantly change in SGC-7901 HGC cells with or without OCT treatment. The relative intensity of Fas and FasL protein expression were also enhanced, but the relative intensity of P53 protein expression was decreased in SGC-7901 HGC cells (5.5 ± 0.3 vs 3.2 ± 0.1, 5.1 ± 0.3 vs 4.5 ± 0.1, 3.3 ± 0.2 vs 4.9 ± 0.3, P 〈 0.05 or 0.01). The relative intensity of P21, P27 and c-myc protein expression did not change. However, G0/G1, S, G2/M stage did not significantly change in SGC-7901 HGC cells with or without OCT treatment.CONCLUSION: Our data suggest that OCT leading to apoptosis is associated with downregulation of mutant-type P53 and up-regulation of Fas and FasL in SGC-7901 HGC cells.
出处 《世界华人消化杂志》 CAS 北大核心 2009年第7期694-698,共5页 World Chinese Journal of Digestology
关键词 胃肿瘤 凋亡 奥曲肽 FAS FASL P53 逆转录多聚酶链反应:流式细胞术 Stomach neoplasm Apoptosis Oc-treotide Fas FasL P53 Reverse transcriptionpolymerase chain reaction Flow cytometry
  • 相关文献

参考文献4

二级参考文献17

  • 1He SW,Shen KQ,He YJ,Xie B,Zhao YM.Regulatory effect and mechanism of gastrin and its antagonists on colorectal carcinoma[J].World Journal of Gastroenterology,1999,5(5):408-416. 被引量:20
  • 2王楠,林洪丽,吴泰华,孙艳玲,谢华,王玲,刘越坚.TIMP-1抑制大鼠肾小球系膜细胞凋亡与磷脂酰肌醇3激酶/丝/苏氨酸激酶通路的研究[J].中国实用内科杂志:临床前沿版,2006,26(7):1059-1061. 被引量:6
  • 3李健玲,罗佐杰,秦映芬,韦敏怡,梁杏欢,冼晶,卢德成,沈昱,何志恒,Jack Y.YANG,Mary Qu YANG.人类端粒酶逆转录酶hTERT Ki-67及p27^(kip1)在嗜铬细胞瘤组织的表达及意义研究[J].中国实用内科杂志:临床前沿版,2006,26(11):1788-1790. 被引量:2
  • 4Cattaneo MG,Amoroso D,Gussoni G,et al.A somatostatin analogue inhibits MAP kinase activation and cell proliferation in human neuroblastoma and in human small cell lung carcinoma cell lines [J].FEBS Lett,1996,397:164.
  • 5Woltering EA,Watson JC,Alperin Lea PC,et al.Somatostatin analogs: Angiogenesis inhibitors with novel mechanisms of action [J].Invest New Drugs,1997,15:77.
  • 6Georgii-Hemming BP,Stromberg T,Janson ET,et al.The somatostatin analog octreotide inhibits growth of interleukin-6 (IL-6)-dependent and IL-6-independent human multiple myeloma cell lines [J].Blood,1999,93(5):1724-1731.
  • 7Solary E,Dubrez L,Eymin B.The role of apoptosis the pathogenesis and treatment of disease [J].Eur Respir J,1996,9:1293-1297.
  • 8Oltvai ZN,Milliman CL,Korsmeyer SJ.Bcl-2 heterodimerizes in vivo with a conserved hemology,Bax,that accelerates programmed cell death [J].Cell,1993,74:609-615.
  • 9Cantley LC. The phosphoinositide 3-kinase pathway [ J ]. Science, 2002,296 ( 5573 ) : 1655 - 1657.
  • 10Qian Y,Zhong X,Flynn DC,et al. IL K mediates actin filament rearrangements and cell migration and invasion through PI3K/Akt/ Rac1 signaling[J]. Oncogene,2005,24(19) :3154.

共引文献20

同被引文献33

引证文献5

二级引证文献15

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