Relationship between EGFR expression, copy number and mutation in lung adenocarcinomas

Zhiyong Liang(Chinese Academy of Medical Sciences & Peking Union Medical College), Jing Zhang(Chinese Academy of Medical Sciences & Peking Union Medical College), Xuan Zeng(Chinese Academy of Medical Sciences & Peking Union Medical College), Jie Gao(Chinese Academy of Medical Sciences & Peking Union Medical College), Shafei Wu(Chinese Academy of Medical Sciences & Peking Union Medical College), Tonghua Liu(Chinese Academy of Medical Sciences & Peking Union Medical College)
BMC Cancer
July 19, 2010
Cited by 76Open Access
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Abstract

BACKGROUND: This study was designed to investigate EGFR protein expression, EGFR copy number and EGFR mutations in lung adenocarcinomas, to explore the relationship of the three markers. METHODS: EGFR status was analyzed in surgically resected lung adenocarcinoma samples from 133 Chinese patients by three methods: protein expression (n=133) by standardized immunohistochemistry (IHC), gene copy number (n=133) by fluorescence in situ hybridization (FISH), and mutation analysis using the Scorpion amplification refractory mutation system (ARMS) (n=133). RESULTS: The results showed that 68.4% of the samples were positive by IHC, 42.1% were positive by FISH, and 63.9% contained activating kinase domain mutations. EGFR mutations were more frequent in non-smoking patients (p=0.008), and EGFR mutations were associated with EGFR FISH positivity (p<0.0001). When using 10% positivity and 2+ as cutoffs, EGFR protein expression was significantly correlated with EGFR FISH positivity (p=0.012) and EGFR mutations (p=0.008) after Bonferroni correction. CONCLUSION: EGFR protein expression, EGFR copy number and EGFR mutations were closely related to each other. Standard methods and interpretation criteria need to be established.


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