Single-cell transcriptomic analysis of HPV-related multiphenotypic sinonasal carcinoma uncovers MYB-HPV association

Human papillomavirus (HPV)-related multiphenotypic sinonasal carcinoma (HMSC) is a rare tumor that morphologically resembles high-grade adenoid cystic carcinoma (ACC) but exhibits indolent clinical behavior. Both demonstrate MYB proto-oncogene upregulation, though HMSC lacks the MYB translocation characteristic of ACC. We performed single-cell RNA sequencing on an HMSC tumor and compared expression patterns with published ACC and oropharyngeal squamous cell carcinoma (OPSCC) datasets. Malignant HMSC cells clustered separately from ACC and lacked bicellular luminal and myoepithelial differentiation. A greater proportion of HMSC cells expressing HPV-related genes (HPVon) expressed MYB (83% vs. 62%, p = 0.022) and MYB targets (p = 6.4 × 10<sup>-6</sup>), supporting an HPV-MYB association. Validation in HPV + OPSCC revealed MYB upregulation in HPVon cells from 7/10 tumors (p < 0.05). A 264-gene signature from HPVon HMSC cells correlated with worse prognosis in HPV + OPSCC (p < 0.003), suggesting an alternate role for HPV. Further validation of the HPV-MYB association and gene signature may improve therapeutic strategies in HPV-related malignancies.

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Publication Details

Journal
npj Precision Oncology
Published
2025-11-24
DOI
https://doi.org/10.1038/s41698-025-01164-5
Primary Topic
Head and Neck Surgical Oncology
Type
article
Field-Weighted Citation Impact
0.00

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article

Single-cell transcriptomic analysis of HPV-related multiphenotypic sinonasal carcinoma uncovers MYB-HPV association

Itay Tirosh, Salvatore M. Caruana, Avishai Wizel, Sidharth V. Puram et al.
npj Precision Oncology
Head and Neck Surgical Oncology
article

Single-cell transcriptomic analysis of HPV-related multiphenotypic sinonasal carcinoma uncovers MYB-HPV association

Itay Tirosh, Salvatore M. Caruana, Avishai Wizel, Sidharth V. Puram, Scott H. Troob, Ogoegbunam Okolo, Yotam Drier, William Britton, Michael Mints, William C. Faquin, Anuraag S. Parikh, Matthew D. A. Spence, Victoria Yu, Derrick T. Lin, Isabel Cioffi
article en

Abstract

Human papillomavirus (HPV)-related multiphenotypic sinonasal carcinoma (HMSC) is a rare tumor that morphologically resembles high-grade adenoid cystic carcinoma (ACC) but exhibits indolent clinical behavior. Both demonstrate MYB proto-oncogene upregulation, though HMSC lacks the MYB translocation characteristic of ACC. We performed single-cell RNA sequencing on an HMSC tumor and compared expression patterns with published ACC and oropharyngeal squamous cell carcinoma (OPSCC) datasets. Malignant HMSC cells clustered separately from ACC and lacked bicellular luminal and myoepithelial differentiation. A greater proportion of HMSC cells expressing HPV-related genes (HPVon) expressed MYB (83% vs. 62%, p = 0.022) and MYB targets (p = 6.4 × 10<sup>-6</sup>), supporting an HPV-MYB association. Validation in HPV + OPSCC revealed MYB upregulation in HPVon cells from 7/10 tumors (p < 0.05). A 264-gene signature from HPVon HMSC cells correlated with worse prognosis in HPV + OPSCC (p < 0.003), suggesting an alternate role for HPV. Further validation of the HPV-MYB association and gene signature may improve therapeutic strategies in HPV-related malignancies.

npj Precision OncologyVol. 9(1)
Massachusetts Eye and Ear Infirmary (US), Harvard University (US), Hebrew University of Jerusalem (IL), Washington University in St. Louis (US), Columbia University Irving Medical Center (US), Massachusetts General Hospital (US), Dana-Farber/Harvard Cancer Center (US), Weizmann Institute of Science (IL), Columbia University (US)
Council for Higher Education, National Cancer Institute, National Institute of Dental and Craniofacial Research
Openalex Percentile: Top 45%
Head and Neck Surgical Oncology
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