Capturing the primordial Kras mutation initiating urethane carcinogenesis
The environmental carcinogen urethane exhibits a profound specificity for pulmonary tumors driven by an oncogenic Q 61 L/R mutation in the gene Kras . Similarly, the frequency, isoform, position, and substitution of oncogenic RAS mutations are often unique to human cancers. To elucidate the principl...
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Published in | Nature communications Vol. 11; no. 1; pp. 1800 - 12 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
14.04.2020
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
ISSN | 2041-1723 2041-1723 |
DOI | 10.1038/s41467-020-15660-8 |
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Summary: | The environmental carcinogen urethane exhibits a profound specificity for pulmonary tumors driven by an oncogenic Q
61
L/R mutation in the gene
Kras
. Similarly, the frequency, isoform, position, and substitution of oncogenic RAS mutations are often unique to human cancers. To elucidate the principles underlying this RAS mutation tropism of urethane, we adapted an error-corrected, high-throughput sequencing approach to detect mutations in murine
Ras
genes at great sensitivity. This analysis not only captured the initiating
Kras
mutation days after urethane exposure, but revealed that the sequence specificity of urethane mutagenesis, coupled with transcription and isoform locus, to be major influences on the extreme tropism of this carcinogen.
Why the carcinogen urethane causes only lung tumours driven by a specific oncogenic mutation in just one
Ras
gene in mice is unclear. Here, the authors capture mutations immediately after urethane exposure and show that the sequence specificity of mutagenesis, transcriptional status, and
Ras
genetic loci may all contribute to this specificity. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-020-15660-8 |