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肺癌中表皮生长因子受体过表达与女性、非吸烟、腺癌和基因突变的关系 被引量:12

Association of epidermal growth factor receptor over-expression with female,non-smoking,adenocarcinoma and gene mutation
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摘要 目的探讨女性和非吸烟的肺腺癌标本中表皮生长因子受体(EGFR)过表达与EG- FR基因突变的关系。方法应用组织微阵列和免疫组织化学方法检测137例国人非小细胞肺癌标本(鳞癌71例、腺癌66例)中EGFR的表达,采用测序的方法检测EGFR基因突变。结果EG- FR过表达率在肺鳞癌中为63.4%显著高于腺癌的43.9%(P<0.05),其与性别、吸烟情况无关,也与基因突变无关。结论EGFR的过表达率在女性、非吸烟、腺癌及存在EGFR突变的标本中未见升高,提示这些人群中EGFR抑制剂效果较好的原因与蛋白过表达无关。 Objective To evaluate the association of adenoeareinoma, female, non-smoking and epidermal growth factor receptor (EGFR) gene mutations with EGFR expression levels in non-small-cell lung cancer (NSCLC) samples. Methods 137 NSCLC samples (71 squamous cell carcinomas and 66 adenoeareinomas) constructed into tissue micro-array were investigated for EGFR expression by immunohistoehemistry. EGFR mutations in exon 19 and exon 21 were determined by sequencing. Results EGFR was more often over-expressed in squamous cell carcinoma samples than adenoeareinomas ( 63.4% vs 43.9 %, P 〈 0.05 ). Expression level was not related to gender, smoking status, and EGFR mutational status. Logistic regression also failed to show association of these parameters with EGFR over-expression. Conclusion Higher efficiency of EGFR inhibitors in NSCLC patients of East Asian ethnics, female, non- smoking and tumors carrying EGFR activating mutations can not be attributed to EGFR expression level differences.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2007年第8期973-974,共2页 Chinese Journal of Experimental Surgery
基金 北京市海淀区科技资助项目(K200446)
关键词 表皮生长因子 肺癌 突变 Epidermal growth factor Lung carcinoma Mutation
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  • 1高尚志.我国心胸外科实验研究目前的热点和问题[J].中华实验外科杂志,2006,23(9):1031-1032. 被引量:3
  • 2Hirsch FR, Witta S. Biomarkers for prediction of sensitivity to EGFR inhibitors in non-small cell lung cancer. Curt Opin Oncol,2005,17 : 118-122.
  • 3Cappuzzo F, Hirsch FR, Rossi E, et al. Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer. J Natl Cancer Inst ,2005,97:643-655.
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  • 6Gazdar AF, Minna JD. Inhibition of EGFR signaling: all mutations are not created equal. PLoS Med ,2005,2 : 1085-1087.

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