AI Article Synopsis

  • The incidence of tongue cancer in young patients is increasing and lacks identified risk factors or molecular markers, indicating it's not yet classified as a separate cancer type.
  • The analysis of head and neck cancer data revealed mutational patterns that helped differentiate between oral cancers and laryngeal cancers based on clinical characteristics.
  • Findings showed that NIRF oral cancers have heightened mutational activities related to internal biological clocks, specific gene mutations, and reactions to microbial influences, suggesting their development may be linked to increased internal mutagenesis due to these factors.

Article Abstract

The incidence of the mobile tongue cancer in young patients has been rising. This oral cancer (OC) type has no identified risk factors (NIRF), no established molecular markers and is not yet recognized as a distinct clinical entity. To understand this emerging malignancy, we innovatively analyzed the public head and neck cancer multi-omics data. We identified mutational signatures that successfully stratified 307 OC and 109 laryngeal cancer cases according to their clinico-pathological characteristics. The NIRF OCs exhibited significantly increased activities of endogenous clock-like and APOBEC-associated mutagenesis, alongside specific cancer driver gene mutations, distinct methylome patterns and prominent antimicrobial transcriptomic responses. Furthermore, we show that mutational signature SBS16 in OCs reflects the combined effects of alcohol drinking and tobacco smoking. Our study characterizes the unique disease histories and molecular programs of the NIRF OCs revealing that this emerging cancer subtype is likely driven by increased endogenous mutagenesis correlated with responses to microbial insults.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10760302PMC
http://dx.doi.org/10.1101/2023.12.15.23299866DOI Listing

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