AbstractHigh-risk human papillomaviruses (HPV-HR) are viruses with a mucosal tropism whose persistence is responsible for the development of cancers. HPV-HR is found in almost 100 % of cervical cancers, 80 % of anal cancers, 50 % of genital cancers and 30 % of ENT cancers. HPV-HR oncoproteins E6 and E7, viral genome integration and epigenetic mechanisms all play a part in setting up the carcinogenic process. Biological markers associated with the presence of pre-cancerous or cancerous lesions include HPV-HR typing, pl6/Ki67 double immunostaining, viral or cellular gene methylation analysis, viral genome integration and serology directed against viral oncoproteins. However, not all these markers have the same performance, and this varies according to the type of cancer. For cervical cancer, HPV-HR typing plays a central role in screening, while other biomarkers, notably methylation, still need to be evaluated and automated before they can find their place in the screening algorithm. In the case of anal cancer, HPV16 typing has recently been incorporated into the screening algorithm, while methylation and serology have yet to benefit from clinical validation to confirm their value. HPV-related ENT cancers do not currently benefit from relevant screening biomarkers. The new biomarkers that have been developed often have very good sensitivity, but insufficient specificity to be used as part of a screening strategy.
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