Please use this identifier to cite or link to this item: https://doi.org/10.1158/1078-0432.CCR-10-2185
Title: Genomic profiles specific to patient ethnicity in lung adenocarcinoma
Authors: Broët, P.
Dalmasso, C.
Tan, E.H. 
Alifano, M.
Zhang, S.
Wu, J.
Lee, M.H.
Régnard, J.-F.
Lim, D.
Koong, H.N.
Agasthian, T.
Miller, L.D.
Lim, E.
Camilleri-Broët, S.
Tan, P. 
Issue Date: 1-Jun-2011
Source: Broët, P., Dalmasso, C., Tan, E.H., Alifano, M., Zhang, S., Wu, J., Lee, M.H., Régnard, J.-F., Lim, D., Koong, H.N., Agasthian, T., Miller, L.D., Lim, E., Camilleri-Broët, S., Tan, P. (2011-06-01). Genomic profiles specific to patient ethnicity in lung adenocarcinoma. Clinical Cancer Research 17 (11) : 3542-3550. ScholarBank@NUS Repository. https://doi.org/10.1158/1078-0432.CCR-10-2185
Abstract: Purpose: East-Asian (EA) patients with non-small-cell lung cancer (NSCLC) are associated with a high proportion of nonsmoking women, epidermal growth factor receptor (EGFR)-activating somatic mutations, and clinical responses to tyrosine kinase inhibitors. We sought to identify novel molecular differences between NSCLCs from EA and Western European (WE) patients. Experimental Design: A total of 226 lung adenocarcinoma samples from EA (n = 90) and WE (n = 136) patients were analyzed for copy number aberrations (CNA) by using a common high-resolution SNP (single nucleotide polymorphism) microarray platform. Univariate and multivariate analyses were carried out to identify CNAs specifically related to smoking history, EGFR mutation status, and ethnicity. Results: The overall genomic profiles of adenocarcinomas from EA and WE patients were highly similar. Univariate analyses revealed several CNAs significantly associated with ethnicity, EGFR mutation, and smoking, but not to gender, and KRAS or p53 mutations. A multivariate model identified four ethnic-specific recurrent CNAs - significantly higher rates of copy number gain were observed on 16p13.13 and 16p13.11 in EA tumors, whereas higher rates of genomic loss on 19p13.3 and 19p13.11 were observed in tumors from WE patients. We identified several potential driver genes in these regions, showing a positive correlation between cis-localized copy number changes and transcriptomic changes. Conclusion: 16p copy number gains (EA) and 19p losses (WE) are ethnic-specific chromosomal aberrations in lung adenocarcinoma. Patient ethnicity should be considered when evaluating future NSCLC therapies targeting genes located on these areas. ©2011 AACR.
Source Title: Clinical Cancer Research
URI: http://scholarbank.nus.edu.sg/handle/10635/110098
ISSN: 10780432
DOI: 10.1158/1078-0432.CCR-10-2185
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