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The mutational landscapes of genetic and chemical models of Kras-driven lung cancer

Peter M. K. Westcott, Kyle D. Halliwill, Minh D. To, Mamunur Rashid, Alistair G. Rust, Thomas M. Keane, Reyno Delrosario, Kuang-Yu Jen, Kay E. Gurley, Christopher J. Kemp, Erik Fredlund, David A. Quigley, David J. Adams and Allan Balmain ()
Additional contact information
Peter M. K. Westcott: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
Kyle D. Halliwill: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
Minh D. To: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
Mamunur Rashid: Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK
Alistair G. Rust: Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK
Thomas M. Keane: Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK
Reyno Delrosario: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
Kuang-Yu Jen: University of California San Francisco
Kay E. Gurley: Fred Hutchinson Cancer Research Center
Christopher J. Kemp: Fred Hutchinson Cancer Research Center
Erik Fredlund: Science for Life Laboratory, Karolinska Institute, Stockholm 171 21, Sweden
David A. Quigley: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco
David J. Adams: Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK
Allan Balmain: Helen Diller Family Comprehensive Cancer Center, University of California San Francisco

Nature, 2015, vol. 517, issue 7535, 489-492

Abstract: Whole-exome sequencing is used to compare the mutational landscape of adenomas from three mouse models of non-small-cell lung cancer, induced either by exposure to carcinogens or by genetic mutation of Kras; the results reveal that the two types of tumour have different mutational profiles and adopt different routes to tumour development.

Date: 2015
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DOI: 10.1038/nature13898

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