Author/Authors :
Marcin Imielinski، نويسنده , , Alice H. Berger، نويسنده , , Peter S. Hammerman، نويسنده , , Bryan Hernandez، نويسنده , , Trevor J. Pugh، نويسنده , , Eran Hodis، نويسنده , , Jeonghee Cho، نويسنده , , James Suh، نويسنده , , Marzia Capelletti، نويسنده , , Andrey Sivachenko، نويسنده , , Carrie Sougnez، نويسنده , , Daniel Auclair، نويسنده , , Michael S. Lawrence، نويسنده , , Petar Stojanov، نويسنده , , Kristian Cibulskis، نويسنده , , Kyusam Choi، نويسنده , , Luc de Waal، نويسنده , , Tanaz Sharifnia، نويسنده , , Angela Brooks-Wilson، نويسنده , , Heidi Greulich، نويسنده , , et al.، نويسنده ,
Abstract :
Lung adenocarcinoma, the most common subtype of non-small cell lung cancer, is responsible for more than 500,000 deaths per year worldwide. Here, we report exome and genome sequences of 183 lung adenocarcinoma tumor/normal DNA pairs. These analyses revealed a mean exonic somatic mutation rate of 12.0 events/megabase and identified the majority of genes previously reported as significantly mutated in lung adenocarcinoma. In addition, we identified statistically recurrent somatic mutations in the splicing factor gene U2AF1 and truncating mutations affecting RBM10 and ARID1A. Analysis of nucleotide context-specific mutation signatures grouped the sample set into distinct clusters that correlated with smoking history and alterations of reported lung adenocarcinoma genes. Whole-genome sequence analysis revealed frequent structural rearrangements, including in-frame exonic alterations within EGFR and SIK2 kinases. The candidate genes identified in this study are attractive targets for biological characterization and therapeutic targeting of lung adenocarcinoma.
