EGFR-activating mutations, DNA copy number abundance of ErbB family, and prognosis in lung adenocarcinoma
Journal
Oncotarget
Journal Volume
7
Journal Issue
8
Pages
9017-9025
Date Issued
2016
Author(s)
Chen H.-Y.
Liu C.-H.
Chang Y.-H.
Ho B.C.
Hsu C.-P.
Yang T.-Y.
Chen K.-C.
Hsu K.-H.
Tseng J.-S.
Hsia J.-Y.
Chuang C.-Y.
Chang C.-S.
Li Y.-C.
Li K.-C.
Chang G.-C.
Abstract
In this study, EGFR-activating mutation status and DNA copy number abundances of members of ErbB family were measured in 261 lung adenocarcinomas. The associations between DNA copy number abundances of ErbB family, EGFR-activating mutation status, and prognosis were explored. Results showed that DNA copy number abundances of EGFR, ERBB2, ERBB3, and ERBB4 had associations with overall survival in lung adenocarcinoma with EGFR-activating mutations. In the stratification analysis, only ERBB2 showed significant discrepancy in patients carrying wild type EGFR and other members of ErbB family in patients carrying EGFR-activating mutation. This indicated that CNAs of ErbB family had effect modifications of EGFR-activating mutation status. Findings of this study demonstrate potential molecular guidance of patient management of lung adenocarcinoma with or without EGFR-activating mutations.
SDGs
Other Subjects
epidermal growth factor receptor; epidermal growth factor receptor 2; epidermal growth factor receptor 3; epidermal growth factor receptor 4; EGFR protein, human; epidermal growth factor receptor; epidermal growth factor receptor 2; epidermal growth factor receptor 3; epidermal growth factor receptor 4; ERBB2 protein, human; ERBB3 protein, human; ERBB4 protein, human; Article; cancer prognosis; cancer survival; controlled study; disease association; exon; female; gene deletion; gene dosage; gene mutation; genetic association; human; human tissue; lung adenocarcinoma; male; mutational analysis; overall survival; survival prediction; wild type; adenocarcinoma; enzyme activation; gene dosage; genetics; lung tumor; metabolism; mortality; pathology; Adenocarcinoma; Enzyme Activation; Female; Gene Dosage; Humans; Lung Neoplasms; Male; Receptor, Epidermal Growth Factor; Receptor, ErbB-2; Receptor, ErbB-3; Receptor, ErbB-4
Publisher
Impact Journals LLC
Type
journal article