期刊文献+

非小细胞肺癌组织中表皮生长因子受体与磷酸化Akt蛋白的表达及其意义 被引量:3

Epidermal growth factor receptor and phophorylated Akt protein expression in non-small-cell lung cancer
原文传递
导出
摘要 目的评价非小细胞肺癌(NSCLC)标本中表皮生长因子受体(EGFR)与其信号传导通路下游的磷酸化Akt(p-Akt)蛋白质表达的意义。方法制作189例非小细胞肺癌标本的组织微阵列,运用免疫组织化学方法检测肺癌组织中的EGFR和p-Akt蛋白质的表达,分析该两种蛋白表达与患者预后生存之间的关系。结果EGFR在NSCLC中的阳性表达率为54.5%(103/189),单因素分析提示其表达程度与性别(χ^2=4.267,P=0.039),病理类型(χ^2=14.749,P=0.002),分化程度(χ^2=6.295,P=0.043)以及病理分期(χ^2=9.318,P=0.025)相关,而Logistic多因素回归分析显示EGFR表达仅与病理类型之间的相关性具有统计学意义(P=0.047)。p-Akt在NSCLC中的阳性表达率为51.3%(97/189),其阳性表达率与各临床病理特征无关(P〉0.05)。二者阳性表达均与预后无关(P值分别为0.972和0.903)。结论NSCLC中EGFR和p-Akt蛋白质阳性表达率对患者预后无提示意义,尚不能以EGFR或p-Akt蛋白质表达作为NSCLC分子分期或判断预后的指标。 Objective To evaluate the expressions of epidermal growth factor receptor (EGFR) and phosphorylated Akt (p-Akt) in non-small-cell lung cancer (NSCLC). Methods 189 NSCLC samples were made into tissue microarray and immunohistochemistry was used to detect the expression of EGFR and p-Akt proteins. The association of the expressions of EGFR and p-Akt protein with the survival time was evaluated. Results The EGFR and p-Akt protein positive rates were 54. 5% and 51.3% respectively. Univariate analysis showed that the EGFR expression was associated with gender(χ^2= 4. 267, P = 0. 039 ), histology(χ^2 = 14. 749, P = 0. 002 ), differentiation (χ^2 = 6. 295, P = 0. 043 ), and pathological stage (χ^2 = 9. 318, P = 0. 025 ). Logistic multivariate analysis showed that only the pathological type was associated with EGFR expression( P = 0. 047 ). The p-Akt expression was not related with the above clinicopathological features( P 〉0. 05 )Kaplan-Meire survival analysis showed that neither of the two proteins had an impact on the patients' survival (P = 0. 972 and P = 0. 903 respectively). Conclusion Protein expressions of IEGFR and p-Akt have no impact on NSCLC patients' survival, thus so far they can not serve as molecular staging or prognostic indicators.
出处 《中华医学杂志》 CAS CSCD 北大核心 2008年第15期1062-1065,共4页 National Medical Journal of China
关键词 非小细胞肺 表皮生长因子受体 磷酸化AKT Carcinoma,non-small-cell lung Receptor,epidermal growth factor Phosphorylated Akt
  • 相关文献

参考文献16

  • 1Ettinger DS. Clinical implications of EGFR expression in the development and progression of solid tumors: focus on non-small cell lung cancer. Oncologist, 2006, 11:358-373.
  • 2Balsara BR, Pei J, Mitsuuehi Y, et al. Frequent activation of AKT in non-small cell lung carcinomas and preneoplastic bronchial lesions. Carcinogenesis, 2004, 25:2053-2059.
  • 3Crowell JA, Steele VE, AKT and the phosphatidylinositol 3- kinase/AKT pathway: important molecular targets for lung cancer prevention and treatment. J Nail Cancer lnst, 2003,95:252-253.
  • 4Hirsch FR, Varella-Garcia M, Bunn PA Jr, et al. Epidermal growth factor receptor in non-small-cell lung carcinomas: correlation between gene copy number and protein expression and impact on prognosis. J Clin Oncol, 2003, 21:3798-3807.
  • 5Cappuzzo F, Magrini E, Ceresoli GL, et al. Akt phosphorylation and gefifinib efficacy in patients with advanced non-small-cell lung cancer. J Nail Cancer Last, 2004, 96:1133-1141.
  • 6Han SW, Hwang PG, Chung DH, et al. Epidermal growth factor receptor (EGFR) downstream molecules as response predictive markers for gefitinib (Iressa, ZD1839 ) in chemotherapy-resistant non-small cell lung cancer. Int J Cancer, 2005, 113 : 109-115.
  • 7Canfley LC. The phosphoinositide 3-kinase pathway. Science, 2002, 296 : 1655-1657.
  • 8Mukohara T, Kudoh S, Yamauehi S, et al. Expression of epidermal growth factor receptor (EGFR) and downstreamactivated peptides in surgically excised non-small-cell lung cancer (NSCLC). Lung Cancer, 2003, 41:123-130.
  • 9Suzuki S, Igarashi S, Hanawa M, et al. Diversity of epidermal growth factor receptor-mediated activation of downstream molecules in human lung carcinomas. Mod Pathol, 2006, 19:986-998.
  • 10David O, Jett J, LeBeau H, et al. Phospho-Akt overexpression in non-small cell lung cancer confers significant stage-independent survival disadvantage. Clin Cancer Res, 2004, 10:6865-6871.

同被引文献32

  • 1汤建民,何权瀛,常秀军.磷酸化Akt蛋白表达在非小细胞肺癌中的临床意义[J].中国呼吸与危重监护杂志,2005,4(3):193-197. 被引量:9
  • 2董强刚,黄进肃,黄建,卢丽琴,杨立民.肺癌靶向治疗研究进展与我国肺癌的EGFR基因突变概况[J].肿瘤,2005,25(6):625-628. 被引量:35
  • 3苗丽君,王静,李珊珊,吴逸明,吴拥军,王新朝.非小细胞肺癌组织中P27表达及定位与磷酸化AKT的关系[J].癌症,2006,25(10):1216-1220. 被引量:7
  • 4CORTAS T,EISENBERG R,FU P,et al.Activation state egfr and STAT-3 as prognostic markers in resected non-small cell lung cancer[J].Lung Cancer,2007,55(3):349-355.
  • 5ZHENG Z,BEPLER G,CANTOR A,et al.Small tumor size and limited smoking history predicts activated epidermal growth factor receptor in early-stage non-small cell lung cancer[J].Chest,2005,128(1):308-316.
  • 6LEE S H,KIM H S,PARK W S,et al.Non-small cell lung cancers frequently express phosphorylated Akt:an immunohistochemical study[J].APMIS,2002,110(7-8):587-592.
  • 7MIYANAGA A,GEMMA A,ANDO M,et al.E-cadherin expression and epidermal growth factor receptor mutation status predict outcome in non-small cell lung cancer patients treated with gefitinib[J].Onco Rep,2008,19(2):377-383.
  • 8SONNWEBER B,DLASKA M,SKYORTSOV S,et al.High predictive value of epidermal growth factor receptor phosphorylation but not of EGFRⅧ mutation in resected stageⅠ non-small cell lung cancer(NSCLC)[J].J Clin Pathol,2006,59(3):255-259.
  • 9TSURUTANI J,FUKUOKA J,TSURUTANI H,et al.Evaluation of two phosphorylation sites improves the prognostic significance of Akt activation in non-small cell lung cancer tumors[J].J Clin Oncol,2006,24(2):306-314.
  • 10SHAH A,SWAIN W A,RICHARDSON D,et al.Phospho-Akt expression is associated with a favorable outcome in non-small cell lung cancer[J].Clin Cancer Res,2005,11(8):2930-2936.

引证文献3

二级引证文献6

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