期刊文献+

转录因子Oct-4在肺癌中的表达及对其生长、增殖的影响 被引量:4

Expression of Oct-4 on lung cancer cells and its role in growth and proliferation
下载PDF
导出
摘要 目的观察Oct-4蛋白在肺癌组织及肺癌细胞系中的表达,探讨Oct-4对肺癌细胞生长、增殖的影响。方法比较正常组织、肺癌组织,正常肺细胞系和肺癌细胞系中Oct-4的表达水平;选取高表达Oct-4的肺癌细胞系,运用siRNA技术降低Oct-4表达,通过MTT实验、BrdU掺入实验等技术检测肺癌细胞的生长、增殖,并检测PI3K分子的表达变化。结果 Oct-4在肺癌组织及肺癌细胞中表达上调,分别与正常组织及HBE比较差异有统计学意义(P<0.05);降低Oct-4表达后,细胞BrdU掺入率明显降低(P<0.05),生长速度减慢(P<0.05),PI3K水平明显降低。结论 Oct-4在肺癌组织及肺癌细胞中表达升高,并通过PI3K促进肺癌细胞生长及增殖。 Objective To investigate the expression of Oct4 on lung cancer cells and its role in their growth and proliferation. Methods Lung cancer tissues and lung cancer cell lineswere selected. The expression of Oct4 was detected by Western blot. Oct- 4 gene expression was reduced by siRNA. The effect of Oct4 on growth and proliferation of lung cancer cells was measured by BrdU labeling and MTT assay, and the change in PI3K expression was detected. Results Compared with normal lung tissue and control cell group, Oct4 level significantly increased (P 〈 0.05 ). BrdU labeling showed that incorporation efficiency of BrdU was higher in siRNA group than in control group and vector group (P 〈 0.05 ). And we also found that after suppressing Oct-4 level, growth velocity of lung cancer cells was negative acceleration (P 〈 0.05). Western blot displayed that the level of PI3K reduced with the decrease of Oct-4 level. Conclusion The expression of Oct4 issignificantly increased in lung cancer tissue and cancer ceils, and Oct4 promotes the growth and proliferation of lung cancer cell via PI3K pathway.
机构地区 解放军第 解放军第
出处 《临床军医杂志》 CAS 2014年第5期454-457,共4页 Clinical Journal of Medical Officers
关键词 OCT4 PI3K 肺肿瘤 增殖 Oct4 PI3 K lung cancer proliferation
  • 相关文献

参考文献6

二级参考文献99

共引文献77

同被引文献33

  • 1热孜宛古丽·约麦尔,阿米娜·沙吾提,买买提·司马义,张晓玲,王慧琴,吴卫东.干细胞相关转录因子OCT4在宫颈癌组织和外周血中的表达及其临床意义[J].现代医学,2021,49(4):411-416. 被引量:2
  • 2殷香保,王捷.纤维蛋白胶的临床应用进展[J].岭南现代临床外科,2003,3(1):67-69. 被引量:11
  • 3O ' REILLY LA, CULLEN L,VISVADER J, et al. The pro- apoptotic BH3-only protein Bim is expressed in hematopoi- etic, epithelial, neuronal, and germ cells [ J ]. Am J Path, 2000,157 (2) :449-461.
  • 4Gu G, Yuan J, Wills M, et al. Prostate cancer cells with stem celcharacteristics reconstitute the original human tumor in vivo [ J]. Cancer Res,2007,67 (10) :4807-4815.
  • 5Chen Z, Xu W R, Qian H, et al. Oct4, a novel marker for human gas-tric cancer [ J ]. J Surg Oncol, 2009,99 ( 7 ) : 414-419.
  • 6Jiang Z, Zheng X, Lytle RA, et al. Lovastatin-induced up- regulation of the BH3-only protein, Bim, and cell death in glioblastoma ceils [ J ]. J Neurochem, 2004,89 ( 1 ) : 168- 178. S.
  • 7unters A, Fernandez de Mattos S, Stahl M, et al. FoxO3a transcriptional regulation of Bim controls apoptosis in pacli- taxel-treated breast cancer cell lines [ J ]. J Biol Chem, 2003,278 (50) :49795-49805.
  • 8Lee J, Kim HK, Rho JY, et al. The human OCT4 isfomls differ in their ability to confer self-renewal [ J ]. J Biol Chem,2006,281 (44) :33554-33565.
  • 9Sadeghi N, Gerber DE. Targeting the PI3K pathway for cancer therapy [ J ]. Future Med Chem, 2012,4 ( 9 ) : 1153- 1169.
  • 10Dummeler B, Hemmings BA. Physiological roles of PKB / Aktisoforms in development and disease [ J]. Biochem Soc Trans,2007,35 (2) : 231-233.

引证文献4

二级引证文献5

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