期刊文献+

NEDD9在胃癌组织中的表达及意义 被引量:4

原文传递
导出
摘要 目的研究NEDD9在胃癌组织中的表达及意义。方法采用免疫组织化学法检测NEDD9在胃癌组织、癌旁组织中的表达,并用单因素方差分析法研究其与临床病理因素的关系。结果 NEDD9表达阳性率在胃癌组织中比在癌旁组织中高,差异有统计学意义(P<0.05);NEDD9在胃癌中的表达与患者的性别、年龄、肿瘤大小无关(P>0.05),与TNM分期及肿瘤组织分化程度有关(P<0.05)。结论 NEDD9的高表达可以反映人类胃癌的恶性生物学行为及在人类胃癌的发生过程中起着重要作用,对胃癌诊断及判断预后有一定的意义,有可能成为判断胃癌预后的一个生物标记。
出处 《中华临床医师杂志(电子版)》 CAS 2012年第7期134-136,共3页 Chinese Journal of Clinicians(Electronic Edition)
  • 相关文献

参考文献14

  • 1巨大维,孙大志,魏品康.白细胞介素8与胃癌的研究进展[J].中华临床医师杂志(电子版),2011,5(9):2666-2668. 被引量:1
  • 2刘福囝,滕勇,张晓旭,黎瀚,刘璐,孙瑞佳,徐惠绵.miR-210在胃癌组织中的表达及临床意义[J].中华临床医师杂志(电子版),2011,5(9):2701-2703. 被引量:5
  • 3Kong C,Wang C,Wang L. Huang BNEDD9 is a positive regulator of epithelial-nesenchymal transition and promotes invasion in aggressive breast cancer[J].PLoS One,2011.e22666.doi:10.1371/journal.pone.0022666.
  • 4Natarajan M,Stewart JE,Golemis EA. HEFI is a necessary and specific downstream effector of FAK that promotes the migration of glioblastoma cells[J].Oncogene,2006.1721-1732.
  • 5Kim M,Gans J D,Nogueira C. Comparative oncogenomics identifies NEDD9 as a melanoma metastasis gene[J].Cell,2006.1269-1281.
  • 6Budhu A,Forgues M,Ye QH. Prediction of venous metastases,recurrence,and prognosis in hepatocellular carcinoma based on a unique immune response signature of the liver microenvironment[J].Cancer Cell,2006.99-111.
  • 7Kumar S,Tomooka Y,Noda M. Identification of a set of genes with developmentally down-regulated expression in the mouse brain[J].Biochemical and Biophysical Research Communications,1992.1155-1161.
  • 8Tikhmyanova N,Golemis EA. NEDD9 and BCARI Negatively Regulate.E-Cadherin Membrane Localization,and Promote E-Cadherin degradation[J].PLoS One,2011.e22102.doi:10.1371/journal.pone.0022102.
  • 9Li Y,Bavarva JH,Wang Z. HEF1,a novel target of Wnt signaling,promotes colonic cell migration and cancer progression[J].Oncogene,2011.2633-2643.
  • 10Izumchenko E,Singh MK,Plotnikova OV. NEDD9 Promotes Oncogenic Signaling in Mammary Tumor Development[J].Cancer Research,2009.7198-7206.

二级参考文献11

  • 1SHI Yi & JIN YouXin State Key Laboratory of Molecular Biology,Shanghai Institute of Biochemistry and Cell Biology,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai 200031,China.MicroRNA in cell differentiation and development[J].Science China(Life Sciences),2009,52(3):205-211. 被引量:11
  • 2SINGH R K,LOKESHWAR B L.Depletion of intrinsic expression of Interleukin-8in prostate cancer cells causes cell cycle arrest,spontaneous apoptosis and increases the efficacy of chemotherapeu-tic drugs. Molecular Cancer . 2009
  • 3AS Haqqani,JK Sandhu,HC Birnboim.Expression of interleukin-8 promotes neutrophil infiltration and genetic instability in mutatect tumors. Neoplasia . 2000
  • 4Yamada H,Aihara T,Okabe S.Mechanism for Helicobacter pylori stimulation of interleukin-8 production in a gastric epithelial cell line (MKN28):roles of mitogen activated protein kinase and interleukin-1 beta. Biochemical Pharmacology . 2001
  • 5Tsuchiya S,,Fujiwara T,Sato F,et al.MicroRNA-210regulates cancer cell proliferation through targeting fibroblast growth factor receptor-like1(FGFRL1). Journal of Biological Chemistry . 2011
  • 6Farazi TA,Spitzer JI,Morozov P,et al.miRNAs in human cancer. Journal of Paleopathology .
  • 7Greither T,Grochola LF,Udelnow A,Lautenschlger C,Würl P,Taubert H.Elevated expression of microRNAs 155,203,210 and 222 in pancreatic tumors is associated with poorer survival. International Journal of Cancer . 2010
  • 8Gee HE,Camps C,Buffa FM, et al.hsa-miR-210 is a marker of tumor hypoxia and a prognostic factor in head and neck cancer. Cancer . 2010
  • 9Alvarez-Garcia I,Miska EA.MicroRNA functions in animal development and human disease. Development . 2005
  • 10J. A. Foekens,A. M. Sieuwerts,M. Smid.Four miRNAs associated with aggressiveness of lymph node-negative, estrogen receptor-positive human breast cancer. Proceedings of the National Academy of Sciences of the United States of America . 2008

共引文献4

同被引文献37

  • 1Feng Y, Wang Y, Wang Z, et al. The CRTCI-NEDD9 signaling axis mediates lung cancer progession caused by LKBI loss[ J ]. Cancer Res, 2012, 72(24): 6502-6511.
  • 2O'Neill GM, Seo S, Serebriiskii IG. et al. A new central scaffold for metastasis: parsing HEF1/Cas-L/NEDD9. Cancer Res, 2007, 67 (19) : 8975-8979.
  • 3Li Y, Bavarva JH, Wang Z, et al. HEFI, a novel target of Wntsignaling, promotes colonic cell migration and cancer progression. Oncogene, 2011, 30 (23) : 2633-2643.
  • 4Astier A, Mani 6 SN, Avraham H, et al. The related adhesion focal tyrosine kinase differentially phosphorylates pl30Cas and the Cas-like protein, pl05HEF1. J Biol Chem, 1997, 272 (32) : 19719-19724.
  • 5Guo W, Ren D, Chen X, et al. HEF1 promotes epithelial mesenchymal transition and bone invasion in prostate cancer under theregulation of microRNA-145. J Cell Biochem, 2013, 114 (7) : 1606-1615.
  • 6Kim M, Gans JD, Nogueira C, et al. Comparative oncogenomics identifies NEDD9 as a melanoma metastasis gene. Cell, 2006, 125 (7) : 1269-1281.
  • 7Li Y, Bavarva JH, Wang Z, et al. HEF1, a novel target of Wnt signaling, promotes colonic cell migration and cancer progression. Oncogene, 2011, 30 (23) : 2633-2643.
  • 8Speranza MC, Frattini V, Pisati F, et al. NEDD9, a novel target of miR-145, increases the invasiveness of glioblastoma. Oncotarget, 2012, 3 (7) : 723-734.
  • 9Natarajan M, Stewart JE, Golemis EA, et al . HEF1 is a necessary and specific downstream effector of FAK that promotes the migration of glioblastoma cells. Oncogene, 2006, 25 (12) : 1721-1732.
  • 10Kumar S,Tomooka Y,Noda M.Identification of a set of genes with developmentally down-regulated expression in the mouse brain[J].Biochem Biophys Res Commun,1992,185(3):1155-1161.

引证文献4

二级引证文献2

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