Human cancer genomes harbor the mutational signature of tobacco-specific nitrosamines NNN and NNK
Michael KorenjakiD, Nuri A. TemiziD, Stéphane Keïta, Bérénice ChavaneliD, Claire RenardiD, Cécilia Sirand, Vincent CahaisiD, Tanguy Mayel, Karin R. Vevang, Foster C. Jacobs, Jiehong GuoiD, William E. Smith, Marissa K. OramiD, Flaviu TăbăraniD, Ozan AhlatiD, Ingrid CornaxiD, M. Gerard O’SullivaniD, Samrat DasiD, Shuvro Prokash NandiiD, Yuhe ChengiD, Ludmil B. AlexandroviD, Silvia BalboiD, Stephen S. HechtiD, Sergey SenkiniD, François VirardiD, , Jiří ZavadiliD
Abstract
Tobacco usage is linked to multiple cancer types and accounts for a quarter of all cancer-related deaths. Tobacco smoke contains various carcinogenic compounds, including polycyclic aromatic hydrocarbons (PAH), though the mutagenic potential of many tobacco-related chemicals remains largely unexplored. In particular, the highly carcinogenic tobacco-specific nitrosamines NNN and NNK form pre-mutagenic pyridyloxobutyl (POB) DNA adducts. In the study presented here, we identified genome-scale POB-induced mutational signatures in cell lines and rat tumors, while also investigating their role in human cancer. These signatures are characterized by T>N and C>T mutations forming from specific POB adducts damaging dT and dC residues. Analysis of 2,780 cancer genomes uncovered POB signatures in [~]180 tumors; from cancer types distinct from the ones linked to smoking-related signatures SBS4 and SBS92. This suggests that, unlike PAH compounds, the POB pathway may contribute uniquely to the mutational landscapes of certain hematological malignancies and cancers of the kidney, breast, prostate and pancreas.
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