The mutational signature profile of known and suspected human carcinogens in mice

Laura Riva(Wellcome Sanger Institute), Arun R. Pandiri(National Institute of Environmental Health Sciences), Yun Rose Li(UCSF Helen Diller Family Comprehensive Cancer Center), Alastair Droop(Wellcome Sanger Institute), James Hewinson(Wellcome Sanger Institute), Michael A. Quail(Wellcome Sanger Institute), Vivek Iyer(Wellcome Sanger Institute), Rebecca Shepherd(Wellcome Sanger Institute), Ronald A. Herbert(National Institute of Environmental Health Sciences), Peter J. Campbell(Wellcome Sanger Institute), Robert C. Sills(National Institute of Environmental Health Sciences), Ludmil B. Alexandrov(University of California San Diego), Allan Balmain(UCSF Helen Diller Family Comprehensive Cancer Center), David J. Adams(Wellcome Sanger Institute)
Nature Genetics
September 28, 2020
Cited by 165Open Access
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Abstract

Epidemiological studies have identified many environmental agents that appear to significantly increase cancer risk in human populations. By analyzing tumor genomes from mice chronically exposed to 1 of 20 known or suspected human carcinogens, we reveal that most agents do not generate distinct mutational signatures or increase mutation burden, with most mutations, including driver mutations, resulting from tissue-specific endogenous processes. We identify signatures resulting from exposure to cobalt and vinylidene chloride and link distinct human signatures (SBS19 and SBS42) with 1,2,3-trichloropropane, a haloalkane and pollutant of drinking water, and find these and other signatures in human tumor genomes. We define the cross-species genomic landscape of tumors induced by an important compendium of agents with relevance to human health.


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