An integrated genomic analysis of lung cancer reveals loss of DUSP4 in EGFR-mutant tumors

D. Chitale, Y. Gong, B. S. Taylor, S. Broderick, C. Brennan, R. Somwar, B. Golas, L. Wang, N. Motoi, J. Szoke, J. M. Reinersman, J. Major, C. Sander, V. E. Seshan, M. F. Zakowski, V. Rusch, W. Pao, W. Gerald, M. Ladanyi

Research output: Contribution to journalArticlepeer-review

174 Scopus citations


To address the biological heterogeneity of lung cancer, we studied 199 lung adenocarcinomas by integrating genome-wide data on copy number alterations and gene expression with full annotation for major known somatic mutations in this cancer. This showed non-random patterns of copy number alterations significantly linked to EGFR and KRAS mutation status and to distinct clinical outcomes, and led to the discovery of a striking association of EGFR mutations with underexpression of DUSP4, a gene within a broad region of frequent single-copy loss on 8p. DUSP4 is involved in negative feedback control of EGFR signaling, and we provide functional validation for its role as a growth suppressor in EGFR-mutant lung adenocarcinoma. DUSP4 loss also associates with p16/CDKN2A deletion and defines a distinct clinical subset of lung cancer patients. Another novel observation is that of a reciprocal relationship between EGFR and LKB1 mutations. These results highlight the power of integrated genomics to identify candidate driver genes within recurrent broad regions of copy number alteration and to delineate distinct oncogenetic pathways in genetically complex common epithelial cancers.

Original languageEnglish (US)
Pages (from-to)2773-2783
Number of pages11
Issue number31
StatePublished - Aug 6 2009
Externally publishedYes


  • Array comparative genomic hybridization
  • EGFR
  • Expression profiling
  • KRAS
  • Lung adenocarcinoma
  • Microarray

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research


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