An Immunocompetent Mouse Model of HPV16(+) Head and Neck Squamous Cell Carcinoma.

Cell Rep

Lineberger Comprehensive Cancer Center, UNC School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Division of Oral and Craniofacial Health Sciences, UNC Adams School of Dentistry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Cell Biology and Physiology, UNC School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Biomedical Research Imaging Center, UNC School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. Electronic address:

Published: November 2019

AI Article Synopsis

  • The incidence of HPV-related head and neck cancers, particularly oropharyngeal squamous cell carcinoma, is rising, with over 60% of cases linked to the virus.
  • Researchers conducted bioinformatics analyses to categorize HPV-positive tumors based on E6 and E7 expression levels, which are crucial for HPV's cancer-promoting effects.
  • They developed a genetically engineered mouse model to mimic E6/E7 expression in the oropharyngeal area, which, when combined with a mutant PIK3CA gene, produces pre-cancerous lesions and offers a platform to study treatments and immune responses.

Article Abstract

The incidence of human papilloma virus (HPV)-associated head and neck squamous cell carcinoma (HNSCC) is increasing and implicated in more than 60% of all oropharyngeal carcinomas (OPSCCs). Although whole-genome, transcriptome, and proteome analyses have identified altered signaling pathways in HPV-induced HNSCCs, additional tools are needed to investigate the unique pathobiology of OPSCC. Herein, bioinformatics analyses of human HPV(+) HNSCCs revealed that all tumors express full-length E6 and identified molecular subtypes based on relative E6 and E7 expression levels. To recapitulate the levels, stoichiometric ratios, and anatomic location of E6/E7 expression, we generated a genetically engineered mouse model whereby balanced expression of E6/E7 is directed to the oropharyngeal epithelium. The addition of a mutant PIK3CA allele leads to the rapid development of pre-malignant lesions marked by immune cell accumulation, and a subset of these lesions progress to OPSCC. This mouse provides a faithful immunocompetent model for testing treatments and investigating mechanisms of immunosuppression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6870917PMC
http://dx.doi.org/10.1016/j.celrep.2019.10.005DOI Listing

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