Abstract

There is still controversy in the scientific field about whether certain types of cutaneous human papillomaviruses (HPVs) are causally involved in the development of non-melanoma skin cancer (NMSC). Deciphering the etiological role of cutaneous HPVs requires – besides tissue culture systems – appropriate preclinical models to match the obtained results with clinical data from affected patients. Clear scientific evidence about the etiology and underlying mechanisms involved in NMSC development is fundamental to provide reasonable arguments for public health institutions to classify at least certain cutaneous HPVs as group 1 carcinogens. This in turn would have implications on fundraising institutions and health care decision makers to force – similarly as for anogenital cancer – the implementation of a broad vaccination program against “high-risk” cutaneous HPVs to prevent NMSC as the most frequent cancer worldwide. Precise knowledge of the multi-step progression from normal cells to cancer is a prerequisite to understand the functional and clinical impact of cofactors that affect the individual outcome and the personalized treatment of a disease. This overview summarizes not only recent arguments that favor the acceptance of a viral etiology in NMSC development but also reflects aspects of causality in medicine, the use of empirically meaningful model systems and strategies for prevention.

Highlights

  • Specialty section: This article was submitted to Virology, a section of the journal Frontiers in Microbiology

  • Non-melanoma skin cancer principally refers to cancer derived from keratinocytes (Small et al, 2016) and can be further divided into basal cell carcinomas (BCCs) and squamous cell carcinomas (SCCs), with relative frequencies of 80 and 20%, respectively (Eisemann et al, 2014)

  • Such effects on tissue homeostasis are of profound importance in nonmelanoma skin cancer (NMSC) development, when human papillomaviruses (HPVs)-infected skin is cumulatively exposed to UV

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Summary

The Individual Genotype

Cancer in general is a multi-factorial disease and as individual as the patient, a reasonable concept that is culminating in the contemporary discourse of personalized medicine (reviewed in Mavropoulos et al, 2014; Harwood et al, 2016). In the case of patients suffering from the rare hereditary disease Epidermodysplasia verruciformis (EV), mutations within at least two genes of homologous transmembrane channel-like (TMC) proteins, TMC6 (EVER1) and TMC8 (EVER2) were described (Lazarczyk et al, 2009, 2012) These proteins are involved in zinc homeostasis and are expressed in keratinocytes, and in lymphocytes, suggesting additional functions in the immune response (reviewed in Kalinska-Bienias et al, 2016). Due to their interaction with the Zn2+ transporter protein ZnT-1, TMC6/8 can further modulate MAP kinases and in turn AP-1, a transcription factor involved in many signal transduction pathways (reviewed in Lazarczyk and Favre, 2008)

Immune Status
Sun Exposure
Cutaneous Papillomaviruses
Transgenic Mice
Natural Model Systems
CURRENT WORK AND PERSPECTIVES ON VACCINATION AGAINST CUTANEOUS HPVS
Fusion to bacterial flagellin
Findings
CONCLUSION
Full Text
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