期刊文献+

Par3、Par6及aPKC蛋白在胃癌发生、发展中的意义 被引量:3

Expression of Par3,Par6 and a PKC in gastric carcinoma and their significance
下载PDF
导出
摘要 目的探讨Par3、Par6和a PKC在胃癌中的表达及意义。方法采用免疫组化法分别检测Par3、Par6和a PKC三种蛋白在153例胃癌各个位点(即胃癌黏膜层、肿瘤中心、侵袭前沿)及淋巴结转移灶中的表达,并以正常胃黏膜作为对照。结果Par3、Par6和a PKC在胃癌组织各个位点的表达水平均显著低于正常胃黏膜(P<0.01);Par3、Par6、a PKC在胃癌中的表达下调率高于肠型和混合型胃癌(P<0.05,P<0.01,P<0.01),Par6和a PKC在侵袭至浆膜及浆膜外病例中的表达下调率显著高于侵及黏膜及肌层的病例(P均<0.01),伴有淋巴结转移病例中Par6的表达低于不伴有淋巴结转移病例(P>0.05)。结论Par3、Par6和a PKC表达下调促进胃癌的发生、发展。 Purpose To investigate the expression of Par3, Par6 and aPKC in gastric carcinoma and their significance. Method Ex-pression of Par3, Par6 and aPKC, by using immunohistochemistry, was detected in different sites of gastric carcinoma ( including the gastric carcinoma in gastric mucosa, the central area and the invasive front of gastric carcinoma) and the lymph node metastasis, using normal gastric mucosa as controls. Results Expression of Par3, Par6 and aPKC in different sites of gastric carcinoma was lower than in that of normal gastric mucosa (P〈0. 01). Expression of Par3, Par6 and aPKC was obviously lower in gastric carcinoma with gastric phenotype than in that with intestinal phenotype and mixed phenotype of gastric carcinoma (P〈0. 05, P〈0. 01, P〈0. 01);the rate of down-regulation of Par6 and aPKC in gastric carcinoma with invasion to ectoptygma and out of ectoptygma was obviously higher than that in gastric carcinoma which located at mucosa and under mucosa (P both〈0. 01), and the rate of down-regulation of Par6 in gas-tric carcinoma with lymph node metastasis was obviously lower than that with no lymph node metastasis ( P〉0. 05 ) . Conclusions The down-regulation expression of Par3, Par6 and aPKC may promote the carcinogenesis and progression of gastric carcinoma.
出处 《临床与实验病理学杂志》 CAS CSCD 北大核心 2014年第12期1342-1345,共4页 Chinese Journal of Clinical and Experimental Pathology
关键词 胃肿瘤 PAR3 Par6 免疫组织化学 aPKC gastric neoplasms aPKC immunohistochemistry
  • 相关文献

同被引文献26

  • 1吴葆华.癌胚抗原、糖类抗原125、糖类抗原50联合检测对老年胃癌的诊断价值[J].中国老年学杂志,2014,34(2):525-526. 被引量:21
  • 2陈亚丽,唐建武.蛋白激酶C亚型在胃癌中的表达及其意义[J].临床肿瘤学杂志,2007,12(5):372-375. 被引量:1
  • 3Saito Y, Murata-Kamiya N, Hirayama T, et al. Conversion of He- licobacter pylori CagA from senescence inducer to oncogenic driver through polarity-dependent regulation of p21 [ J ]. J Exp Med,2010,207(10) :2157 -74.
  • 4Johnson E M, Gaddy J A, Voss B J, et al. Genes required for as- sembly of pili associated with the Helicibacter pylori tag Type IV secretion system [ J ]. Infect Immun, 2014,82 ( 8 ) :3457 - 70.
  • 5Herrera V, Parsonnet J. Helicobacter pylori and gastric adenocar- cinoma[ J]. Clin Microbiol Infect, 2009,15 ( 11 ) :971 - 6.
  • 6Zhou J, Xie Y, Zhao Y, et al. Human gastrin mRNA expression up-regulated by Helieobacter pylori CagA through MEK/ERK and JAK2-signaling pathways in gastric cancer cells[J]. Gastric Canc- er, 2011,14(4) :322 -31.
  • 7Liu Z, Xu X, Chen L, et al. Helicobaeter pylori CagA inhibits the expression of Runx3 via Src/MEK/ERK and p38MAPK path- ways in gastric epithelial cell[J]. J Cell Biochem, 2012,113 (3) :1080 -6.
  • 8Ramos J W. The regulation of extracellular signalregulated kinase (ERK) in mammalian cells[ J]. Int J Biochem Cell Biol, 2008, 40(12) :2707 - 19.
  • 9Zhao D, Liu Z, Ding J, et al. Helicobacter pylori CagA upregula- tion of CIP2A is dependent on the Src and MEK/ERK pathways [J]. J Med Microbiol, 2010,59(3) :259 -65.
  • 10房静远,刘文忠,李兆申,杜奕奇,纪小龙,戈之铮,李延青,姒健敏,吕农华,吴开春,陈萦晅,萧树东.中国慢性胃炎共识意见[J].胃肠病学,2013,18(1):24-29. 被引量:642

引证文献3

二级引证文献11

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