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PTEN和EGFR在胃癌中的表达及相关性研究 被引量:1

Expression and relationship between PTEN and EGFR in gastric carcinoma
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摘要 目的:检测第10号染色体缺失的磷酸酶和张力蛋白同源物基因PTEN及表皮生长因子受体EGFR在胃癌组织中的表达,探讨两者与胃癌肿瘤行为的关系及意义。方法:采用免疫组织化学染色法(S-P法)检测105例胃癌组织及癌旁正常胃组织中EGFR和PTEN蛋白的表达水平,并将检测结果与临床病理参数进行综合分析。结果:胃癌组织PTEN的表达56.19%明显低于正常组织中的表达的表达92.3%,而胃癌组织EGFR的表达46.67%明显高于正常组织7.62%,(P<0.01)。二者的表达与性别和年龄无相关性(P>0.05),与胃癌的分化程度、浸润深度、淋巴结转移及临床分期有相关性(P<0.05)。结论:PTEN在胃癌组织中呈低表达,EGFR在胃癌组织中存在高表达,与胃癌的发生、发展有一定关系,并与胃癌的分化程度、浸润深度、淋巴结转移及临床分期密切相关,二者呈负相关。 Objective:To investigate expression of PTEN and EGFR in gastric carcinoma and to explore its relationship with the genesis and development of gastric carcinoma and its relationship with clinicopathological parameters. Methods:Immunohistochemistry(S-P) was used to detect the expression of PTEN and EGFR protein in 105 case of gastric carcinoma tissues and their adjacent normal gastric tissues. Results:In the normal gastric tissue,the positive rate of PTEN protein(92.3%) were higher than those in gastric cancer tissue(56.19%) . The over expression of EGFR in gastric carcinoma was higher than that in normal gastric tissues(7.62%) ( P 0. 01) . Their expression were unrelated with gender and age of gastric carcinoma(P0.05) ,but closely correlated with levels of histological differentiation and clinical pathology stages. Conclusions:The PTEN protein expression flaw and over expression of EGFR which may play certain role in the genesis and development of gastric carcinoma and closely related the degree of differentiation,depth of invasion,lymph node metastasis and clinical stages. There was negative trend between PTEN expression and EGFR in gastric carcinoma.
出处 《现代生物医学进展》 CAS 2010年第2期316-319,共4页 Progress in Modern Biomedicine
关键词 PTEN EGFR 胃癌 免疫组织化学 EGFR EGFRvⅢ gastric carcinoma immunohistochemistry
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  • 1Sansal I, Sellers WR.The biology and clinical relevance of the PTEN tumor suppressor pathway[J]. J Clin Oncol, 2004, 22 (14) : 2954- 63. 被引量:1
  • 2Sansal I, Sellers W R. The biology and clinical relevance ofthe PTEN tumor suppressor pathway [J]. Journal of Clinical Oncology, 2004,22 (14) :2954-2963. 被引量:1
  • 3Park M J, Kim MS, Park IC, Kang HS, Yoo H, Park SH, Rhee CH, Hong SI, Lee SH. PTNE suppresses hyaluronic acid-induced matrix metalloproteinase-9 expression in U87MG glioblastoma cells through focal adhesion kinase dephosphorylation[J]. Cancer Res, 2002,62(21): 6318-22. 被引量:1
  • 4JoseB. Why the epidermal growth facot receptor? The rational for cancer therapy[J]. Oneologist, 2002,7(4):2-8. 被引量:1
  • 5于晓棠,陆世伦,朱世能.表皮生长因子受体与肿瘤[J].复旦学报(医学版),2005,32(4):497-500. 被引量:20
  • 6Yaden Y, Sliwkowski MX. Untangling the ErbB signling network [J]. Nat Rev Mol all Biol, 2001,2(2):127-137. 被引量:1
  • 7Attwell S, Mills J, Tmussard A, et al. integration of cell attachment, cytoskeletal localization, andsignaling by integrin-linked kinase (ILK), CH-IL KBI, and the tumor suppressor PTEN [J]. MolBiol Gell, 2003,1 4(12): 4813-4825. 被引量:1
  • 8Kotelevets L, van Hengel J, Bruyneel E, Mareel M, van Roy, F Chastre E.The lipid Phosphatase activity of PTEN is critieal for stabilizing intercellular junetions and reverting invasiveness. J Cell Biol, 2001, 155(7):1129-35. 被引量:1

二级参考文献38

  • 1Moghal N,Stemberg PW. Multiple poeitive and negative regulators of signaling by the EGR-receptor. Current Opinion in Cell Biology, 1999,11:190 被引量:1
  • 2Slieker LJ, Martensen TM, Lane MD. Synthesis of epidermal growth factor receptor in human A431 cells. Glycosylation-dependent acquisition of ligand binding activity occurs post-translationally in the endoplasmic reticulum. J Biol Chem, 1986,261:15233 被引量:1
  • 3Jorissen RN. ,Walker F,Pouliot N, et al. Epidermal growth factor receptor:mechanisms of activation and signaling. Exp Cell Res ,2003,284:31 被引量:1
  • 4Ward CW,Garrett TP. The relationship between the L1 and L2 domains of the insulin and epidermal growth factor receptors and leucine-rich repeat modules. BMC Bio In f,2001,2(1) :4 被引量:1
  • 5Sako Y,Minoghchi S,Yangida T. Single-molecule imaging of EGFR signaling on the surface of living cells.Nat Cell Biol ,2000,2:168 被引量:1
  • 6Mineo C,Gill GN,Anderson RG. Regulated migration of epidermal growth factor receptor from caveolae. J Biol Chem,1999,274:30636 被引量:1
  • 7Yu X,Sharma KD, Takahashi T, et al. Ligand-independent dimer formation of epidermal growth factor receptor (EGFR) is a step separable from ligand-induced EGFR signaling. Mol Bio Cell,2002,13:2547 被引量:1
  • 8Moriki T, Maruyama H, Maruyama IN. Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain. J Mol Biol.2001.311:1011 被引量:1
  • 9Olayioye MA,Neve RM, Lane HA, et al. The EerbB signaling network:receptor heterodimerization in development and cancer. The EMBO J,2001,19(13) :3159 被引量:1
  • 10Yamauchi T,Uekd K,Tobe K,et al.Tyrosine phosphorytation of the EGF receptor by the kinase Jak2 is induced by growth hormone. Nature,1997,390(6655) :91 被引量:1

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