Human Papillomavirus-related tumours of the oropharynx display a lower tumour hypoxia signature. Issue 9 (September 2015)

• Record Type: Journal Article
• Authors: Hanns, Elodie; Job, Sylvie; Coliat, Pierre; Wasylyk, Christine; Ramolu, Ludivine; Pencreach, Erwan; Suarez-Carmona, Meggy; Herfs, Michael; Ledrappier, Sonia; Macabre, Christine; Abecassis, Joseph; Wasylyk, Bohdan; Jung, Alain C.
• Is Part Of: Oral oncology. Volume 51:Issue 9(2015:Sep.)
• Page Start: 848
• Page End: 856
• Publication Date: 2015-09
• Subjects: Head and neck squamous cell carcinoma -- HPV -- Hypoxia -- Transcriptome -- Gene expression -- Immunohistochemistry; Mouth -- Cancer -- Periodicals; Mouth -- Tumors -- Periodicals; Mouth Diseases -- Periodicals; Mouth Neoplasms -- Periodicals; Bouche -- Cancer -- Périodiques; Bouche -- Tumeurs -- Périodiques; Tumeurs -- Périodiques; Electronic journals; 616.9943105
• DOI: 10.1016/j.oraloncology.2015.06.003
• Languages: English
• ISSNs: 1368-8375

Abstract

Highlights: HPV-positive and -negative HNSCC cells lines adapt differently to hypoxia. HPV-positive xenografts display less hypoxic area/cells. HPV-positive OSCC have a lower hypoxia status. HPV-positive OSCC display increased tumour angiogenesis. Improved response to therapy could be linked to these hypoxia properties. Summary: Objectives: Human Papillomavirus (HPV)-related oropharyngeal squamous cell carcinoma (OSCC) patients have improved prognosis compared to other head and neck (HNSCC) cancers. Since poor prognosis is associated with tumour hypoxia, we studied whether the hypoxic response is different in HPV-related cells and tumours. Material and methods: HPV-positive and -negative cells were incubated in hypoxia and analyzed by qRTPCR, western blotting and cell proliferation assays. Tumours formed by xenografting these cells in nude mice were studied by IHC. HNSCC patient samples were analyzed by unsupervised clustering of hypoxia-related gene expression, quantitative real-time PCR (qRTPCR) and immunohistochemical (IHC) detection of neo-blood vessels. Results and conclusion: HPV-positive and -negative cells responded differently to hypoxia, in terms of gene expression (HIF-1α, PHD-3, GLUT-1 and VEGF-A) and cell survival. Tumour xenografts formed by HPV-positive cells had fewer hypoxic areas than those formed by HPV-negative cells. HPV related tumours were less hypoxic, expressed lower levels of hypoxia-responsive genes, and had a higher density of neo-blood vessels. HPV-related OSCC display lower tumour hypoxia, which could be linked to the distinct intrinsic abilities of HPV-positive tumour cells to adapt to hypoxia and to their better prognosis.