Distinct functions of epidermal and myeloid derived VEGF-A in skin tumorigenesis mediated by HPV8

Beta human papillomaviruses (HPV) have been suspected to be carcinogenic in non-melanoma skin cancers (NMSC), but the basis for potential viral contributions to these cancers are poorly understood. In particular, it is unresolved how HPV-infected keratinocytes escape cell cycle control and whether their crosstalk with immune cells is critical for tumorigenesis. In non-viral preclinical models, the angiogenic cytokine VEGF-A has been identified as a critical regulator of NMSC. In this study, we dissected the contribution of epidermal versus myeloid cell-derived VEGF-A in HPV-mediated skin cancer by interbreeding an HPV8 transgenic mouse model with a conditional disruption of VEGF-A restricted to either epidermal or myeloid cells. Whereas only epidermal-derived VEGF-A was essential for initiation of skin tumor development, both spontaneously and UV-light triggered, both epidermal and myeloid cell-derived VEGF-A contributed to regeneration-induced tumorigenesis upon HPV8 overexpression, partly through a paracrine effect on endothelial cells but also most probably through an additional autocrine effect on epidermal cells. Our findings offer new mechanistic insights into distinct functions of epidermal versus myeloid cell-derived VEGF-A during HPV-mediated tumorigenesis, with possible implications for preventing this disease.