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
癌
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