Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

Imielinski, M; Berger, AH; Hammerman, PS; Hernandez, B; Pugh, TJ; Hodis, E; Cho, J; Suh, J; Capelletti, M; Sivachenko, A; Sougnez, C; Auclair, D; Lawrence, MS; Stojanov, P; Cibulskis, K; Choi, K; de Waal, L; Sharifnia, T; Brooks, A; Greulich, H; Banerji, S; Zander, T; Seidel, D; Leenders, F; Ansén, S; Ludwig, C; Engel-Riedel, W; Stoelben, E; Wolf, J; Goparju, C; Thompson, K; Winckler, W; Kwiatkowski, D; Johnson, BE; Jänne, PA; Miller, VA; Pao, W; Travis, WD; Pass, HI; Gabriel, SB; Lander, ES; Thomas, RK; Garraway, LA; Getz, G; Meyerson, M

HERO ID

1597199

Reference Type

Journal Article

Year

2012

Language

English

PMID

22980975

HERO ID 1597199
In Press No
Year 2012
Title Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing
Authors Imielinski, M; Berger, AH; Hammerman, PS; Hernandez, B; Pugh, TJ; Hodis, E; Cho, J; Suh, J; Capelletti, M; Sivachenko, A; Sougnez, C; Auclair, D; Lawrence, MS; Stojanov, P; Cibulskis, K; Choi, K; de Waal, L; Sharifnia, T; Brooks, A; Greulich, H; Banerji, S; Zander, T; Seidel, D; Leenders, F; Ansén, S; Ludwig, C; Engel-Riedel, W; Stoelben, E; Wolf, J; Goparju, C; Thompson, K; Winckler, W; Kwiatkowski, D; Johnson, BE; Jänne, PA; Miller, VA; Pao, W; Travis, WD; Pass, HI; Gabriel, SB; Lander, ES; Thomas, RK; Garraway, LA; Getz, G; Meyerson, M
Journal Cell
Volume 150
Issue 6
Page Numbers 1107-1120
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.
Doi 10.1016/j.cell.2012.08.029
Pmid 22980975
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English