AI Article Synopsis

  • Head and neck squamous cell carcinomas (HNSCC) exhibit diverse features influenced by human papillomavirus (HPV) status, highlighting the need for careful patient stratification in Mexico.
  • A study analyzing 414 Mexican patients revealed that 32.3% tested positive for p16 and 22.3% for HPV, with HPV types 16, 18, and others being the most common.
  • High expression levels of certain genes were linked to poor survival rates, while others indicated better outcomes, and specific signaling pathways were found to be downregulated in HPV-positive cases, providing potential targets for therapy.

Article Abstract

Head and neck squamous cell carcinomas (HNSCC) show a variety of biological and clinical characteristics that could depend on the association with the human papillomavirus (HPV). Biological and clinical characterization is essential to stratify patients based on prognostic and predictive factors. Reports on HNSCC are scarce in Mexico. Herein, we analyzed 414 Mexican patients with HNSCC, including oropharynx (OPSCC), larynx (LASCC), and oral cavity (OCSCC), and identified HPV DNA and p16 expression. Global gene expression profiles were analyzed in 25 HPV+/p16+ vs. HPV-/p16- cases. We found 32.3% p16+ and 22.3% HPV+ samples, HPV 16, 18, 39, 52, and 31 being the most frequent genotypes. For OPSCC, LASCC and OCSCC, 39.2, 14.7, and 9.6% were HPV+/p16+, respectively. High expression of SLIRP, KLF10, AREG, and LIMA was associated with poor survival; in contrast, high expression of MYB and SYCP2 correlated with better survival. In HPV+ cases, high expression of SLC25A39 and GJB2 was associated with poor survival. Likewise, EGFR, IL-1, IL-6, JAK-STAT, WNT, NOTCH, and ESR1 signaling pathways were downregulated in HPV+ cases. CSF1R, MYC, and SRC genes were identified as key hubs and therapeutic targets. Our study offers information regarding the molecular and clinical characteristics of HNSCC in Mexican patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616077PMC
http://dx.doi.org/10.3390/cancers13225602DOI Listing

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