期刊文献+

基于PI3K/Akt/mTOR通路探讨半夏泻心汤对PLGC大鼠黏膜微环境的影响 被引量:7

Effect of Banxia Xiexin decoction on mucosal microenvironment in rat model of PLGC based on the PI3K/Akt/mTOR pathway
原文传递
导出
摘要 目的:对胃癌前病变(Precancerous Lesion of Gastric Cancer,PLGC)模型大鼠从整体、细胞及分子水平的指标进行观察,分析其胃黏膜微环境的特点,并初步探讨半夏泻心汤对其胃黏膜的作用机制。方法:清洁级雄性SD大鼠70只,随机分成3组:模型组50只,造模加中药干预组10只,空白组10只。采用改良MNNG+复合法制备PLGC大鼠模型,于造模中期第10周、造模结束期第20周,各组随机抽取5只大鼠,分别从整体水平、细胞水平及分子水平检测半夏泻心汤对其胃黏膜微环境的影响。结果:1)启动子PTEN,造模加中药干预组较模型组表达高,但仍低于空白组; 2)调控器PI3K/Akt/mTOR信号通路,PI3K、Akt、mTOR的表达造模加中药干预组较模型组低,但仍高于空白组; 3)效应子HIF-1α及其下游基因,造模加中药干预组较模型组表达低,但仍高于空白组;上述结果差异均有统计学意义(P <0. 05)。结论:中药半夏泻心汤通过影响PLGC大鼠胃黏膜组织微环境变化的3个关键环节,即PI3K/Akt/mTOR信号通路中的启动子、调控器及效应子,从而影响并阻断PLGC的发生发展。 Objective:To observe various indices of a rat model of precancerous lesion of gastric cancer(PLGC)at gross,cellular,and molecular levels,to analyze the characteristics of gastric mucosal microenvironment in the rats,and to primarily explore the mechanism of action of Banxia Xiexin decoction on gastric mucosa.Methods:A total of 70 clean male Sprague-Dawley rats were randomly divided into three groups:50 in model group,10 in modeling plus traditional Chinese medicine treatment group(MTCM group),and 10 in blank group.The rat model of PLGC was established by modified MNNG + composite method.At the 10th week of modeling(interim period)and the 20th week of modeling(end period), 5 rats were randomly selected from each group to determine the effect of Banxia Xiexin decoction on gastric mucosal microenvironment in the rats at gross,cellular,and molecular levels.Results:1)The MTCM group had a higher expression level of the promoter PTEN than the model group,but it was still lower than that in the blank group;2)The MTCM group had a lower expression level of the signal pathway regulators PI3K/Akt/mTOR than the model group,but it was still higher than that in the blank group;3)The MTCM group had a lower expression level of the effector HIF-1α and its downstream genes than the model group,but it was still higher than that in the blank group;all the differences in the above results were significant(P<0.05).Conclusion:The traditional Chinese medicine Banxia Xiexin decoction affects and prevents the development and progression of PLGC by involving three key steps in the microenvironmental changes of gastric mucosa in the rats with PLGC,namely promoters,regulators,and effectors in the PI3K/Akt/mTOR signaling pathway.
作者 刘嘉诚 刘洁 LIU Jiacheng;LIU Jie(Tianjin University of Traditional Chinese Medicine,Tianjin 300193,China;The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine,Tianjin 300150,China)
出处 《湖南中医杂志》 2018年第12期117-119,共3页 Hunan Journal of Traditional Chinese Medicine
基金 天津市高等学校科技发展基金计划项目(编号:20140217)
关键词 胃癌前病变 半夏泻心汤 PI3K/Akt/mTOR通路 黏膜微环境 实验研究 precancerous lesion of gastric cancer Banxia Xiexin decoction PI3K/Akt/mTOR pathway mucosalmicroenvironment experimental study
  • 相关文献

参考文献4

二级参考文献95

  • 1Alberts SR, Cervantes A, van de Velde CJ. Gastric cancer: epidemiology,pathology and treatment[ J 1- Ann Oncol, 2003,14 (Suppl 2) :ii31 -36. 被引量:1
  • 2Korkolopoulou p, Patsouris E, Konstantinidou AE, et al. Hypoxia - inducible factor 1 alpha/vascular endothelial growth factor axis in astrocytomas in astrocytomas. Associations with microvessel morphometry, proliferation and prognosis[J]. Neuropathol Appl Neurobiol,2004,30:267 - 278. 被引量:1
  • 3Cummins EP, Taylor CT. Hypoxia -responsive transcription factors [ J]. Ptlugers Arch - Eur J Physiol,2005 ,450 :363 - 371. 被引量:1
  • 4Morgensztern D, McLeod HL. PI3K/Akt/mTOR pathway as a target for cancer therapy[ J]. Anti - Cancer Drugs,2005,16:797 - 803. 被引量:1
  • 5Garcia Z, Kumar A, Marques M, et al. Phosphoinositide 3 - kinase controls early and late events in mammalian cell division [ J ]. EMBO J,2006,25:655 -661. 被引量:1
  • 6Beitner- Johnson D, Rust RT, Hsieh TC, et al. Hypoxia activates Akt and induces phosphorylation of GSK -3 in PC12 cells[ J]. Cell Signal,2001,13:23 -27. 被引量:1
  • 7Kobayashi I, Semba S, Matsuda Y, et al. Significance of Akt phosphorylation on tumor growth and vascular endothelial growth factor expression in human gastric carcinoma[ J ]. Pathobiology,2006,73: 8 - 17. 被引量:1
  • 8Pili R, Donehower RC. Is hif - 1 cta valid therapeutic target [ J ] ? J Nad Cancer Inst,2003 ,95 :498 - 499. 被引量:1
  • 9Namba R, Young LJ, Maglione JE, et al. Selective estrogen receptor modulators inhibit growth and progression of premalignant lesions in a mouse model of ductal carcinoma in situ[ J]. Breast Cancer Res, 2005,7 : R881 - 889. 被引量:1
  • 10Wouters A, Pauwels B, Lardon F, et al. Review : implications of in vitro research on the effect of radiotherapy and chemotherapy under hypoxic conditions[ J]. Oncologist ,2007,12:690 - 712. 被引量:1

共引文献38

同被引文献158

引证文献7

二级引证文献102

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