Abstract
Background: Human papillomavirus (HPV) oncogenes E6, E7, and shorter isoforms of E6 (E6*) are known carcinogenic factors in head and neck squamous cell carcinoma (HNSCC). Little is known regarding E6* functions. Methods: We analyzed RNA-seq data from 68 HNSCC HPV type 16-positive tumors to determine host genes and pathways associated with E6+E7 expression (E6E7) or the percent of full-length E6 (E6%FL). Influence scores of E6E7 and E6%FL were used to test for associations with clinical variables. Results: For E6E7, we recapitulated all major known affected pathways and revealed additional pathways. E6%FL was found to affect mitochondrial processes, and E6%FL influence score was significantly associated with overall survival and tumor size. Conclusions: HPV E6E7 and E6* result in extensive, dose-dependent compensatory effects and dysregulation of key cancer pathways. The switch from E6 to E6* promotes oxidative phosphorylation, larger tumor size, and worse prognosis, potentially serving as a prognostic factor for HPV-positive HNSCC.
Original language | English (US) |
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Pages (from-to) | 2375-2389 |
Number of pages | 15 |
Journal | Head and Neck |
Volume | 42 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1 2020 |
Keywords
- E6
- E6*
- E7
- head and neck cancer
- human papillomavirus
- influence score
- survival
ASJC Scopus subject areas
- Otorhinolaryngology