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The Complexity of Tobacco Smoke-Induced Mutagenesis in Head and Neck Cancer.

Laura TorrensSarah MoodyAna Carolina de CarvalhoMariya KazachkovaBehnoush Abedi-ArdekaniSaamin CheemaSergey SenkinThomas CattiauxRicardo Cortez Cardoso PenhaJoshua R AtkinsValérie GaborieauPriscilia ChopardChristine CarreiraAmmal AbbasiErik N BergstromRaviteja VangaraJingwei WangStephen FitzgeraldCalli LatimerMarcos Diaz-GayDavid JonesJon TeagueFelipe Ribeiro PintoLuiz Paulo KowalskiJerry PoleselFabiola GiudiciJosé Carlos de OliveiraPagona LagiouAreti LagiouMarta VilenskyDana MatesIoan N MatesLidia Mrb ArantesRui Manuel Vieira ReisJose Roberto V PodestaSandra V von ZeidlerIvana HolcatovaMaria Paula CuradoCristina CanovaElenora FabianovaPaula A Rodríguez-UrregoLaura HumphreysLudmil B AlexandrovPaul J BrennanMichael R StrattonSandra Perdomo
Published in: medRxiv : the preprint server for health sciences (2024)
Tobacco smoke, alone or combined with alcohol, is the predominant cause of head and neck cancer (HNC). Here, we further explore how tobacco exposure contributes to cancer development by mutational signature analysis of 265 whole-genome sequenced HNC from eight countries. Six tobacco-associated mutational signatures were detected, including some not previously reported. Differences in HNC incidence between countries corresponded with differences in mutation burdens of tobacco-associated signatures, consistent with the dominant role of tobacco in HNC causation. Differences were found in the burden of tobacco-associated signatures between anatomical subsites, suggesting that tissue-specific factors modulate mutagenesis. We identified an association between tobacco smoking and three additional alcohol-related signatures indicating synergism between the two exposures. Tobacco smoking was associated with differences in the mutational spectra and repertoire of driver mutations in cancer genes, and in patterns of copy number change. Together, the results demonstrate the multiple pathways by which tobacco smoke can influence the evolution of cancer cell clones.
Keyphrases
  • genome wide
  • copy number
  • crispr cas
  • mitochondrial dna
  • gene expression
  • young adults
  • density functional theory
  • diabetic rats
  • stress induced