
doi: 10.1002/rmv.471
pmid: 15942978
The aetiology of squamous cell carcinomas of the head and neck (HNSCC) is multifactorial. Oncogenic human papillomaviruses (HPVs), a causative agent in uterine cervical cancer, have also been repeatedly detected in HNSCC, especially in squamous cell carcinomas of tonsils. Approximately half the HPV DNA-positive HNSCC contain detectable E6/E7 transcripts with wild-type p53, reduced pRb and overexpressed p16 in the tumours. HPV-16 is the predominant type and exists in episomal, integrated, or mixed forms. Tonsillar carcinomas have a remarkably higher viral load than carcinomas at other sites of the head and neck region. HPV-16 DNA has also been detected in tumour-free tonsils. Infection by oncogenic HPVs is a necessary but not a sufficient cause of cancers. Studies on the molecular mechanisms underlying HPV-associated carcinogenesis are difficult, because HPV is not easy to propagate in vitro. HPV-immortalised human tonsillar epithelial cell lines may provide an in vitro model to study co-factors for the HPV-associated tonsillar cancers and to test the effects of anti-viral and anti-tumour agents.
Human papillomavirus 16, Genes, p16, Papillomavirus E7 Proteins, Palatine Tonsil, Papillomavirus Infections, Oncogene Proteins, Viral, Repressor Proteins, Head and Neck Neoplasms, Carcinoma, Squamous Cell, Humans, RNA, Messenger
Human papillomavirus 16, Genes, p16, Papillomavirus E7 Proteins, Palatine Tonsil, Papillomavirus Infections, Oncogene Proteins, Viral, Repressor Proteins, Head and Neck Neoplasms, Carcinoma, Squamous Cell, Humans, RNA, Messenger
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