Abstract

Human papillomaviruses (HPV) replicate their DNA in the suprabasal layer of the infected mucosa or skin. In order to create a suitable environment for vegetative viral DNA replication HPV delay differentiation and sustain keratinocyte proliferation that can lead to hyperplasia. The mechanism underlying cell growth stimulation is not well characterized. Here, we show that the E6 oncoprotein of the βHPV type 8 (HPV8), which infects the cutaneous skin and is associated with skin cancer in Epidermodysplasia verruciformis patients and immunosuppressed organ transplant recipients, binds to the protein tyrosine phosphatase H1 (PTPH1), which resulted in increased protein expression and phosphatase activity of PTPH1. Suppression of PTPH1 in immortalized keratinocytes reduced cell proliferation as well as the level of epidermal growth factor receptor (EGFR). Furthermore, we report that HPV8E6 expressing keratinocytes have increased level of active, GTP-bound Ras. This effect was independent of PTPH1. Therefore, HPV8E6-mediated targeting of PTPH1 might result in higher level of EGFR and enhanced keratinocyte proliferation. The HPV8E6-mediated stimulation of Ras may be an additional step to induce cell growth. Our results provide novel insights into the mechanism how βHPVE6 proteins support proliferation of infected keratinocytes, thus creating an environment with increased risk of development of skin cancer particularly upon UV-induced DNA mutations.

Highlights

  • Infection with human papillomaviruses belonging to the genus beta-papillomavirus, which exhibit a tropism for the cutaneous epithelium, occurs early in life

  • We extended these studies and analyzed an effect of HPV8E6 on the level of endogenous protein tyrosine phosphatase H1 (PTPH1) present in various HPV8E6 expressing immortalized human keratinocyte cell lines and in Normal human epidermal keratinocytes (NHEK)

  • Immunoblotting revealed that HaCaT, RTS3b as well as NHEK had higher amounts of endogenous PTPH1 when HPV8E6 was expressed (Figure 1A)

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Summary

Introduction

Infection with human papillomaviruses belonging to the genus beta-papillomavirus (βHPV), which exhibit a tropism for the cutaneous epithelium, occurs early in life. Persistent infections with certain types of βHPVs are associated with the development of non-melanoma skin cancer at sun-exposed sites. Cells 2019, 8, 244 link between βHPV infection and skin cancer development in immunosuppressed organ transplant recipients (OTR), who have a 100-fold increased risk to develop cutaneous squamous cell carcinomas (cSCC) [2] and a 250-fold increased risk for solar precancerous actinic keratosis (AK) [3,4]. Iatrogenic immunosuppression in OTR allows a more active replication of the commensal βHPV spectrum in the entire skin with the result of higher viral load [2,5]. UV light is an important co-factor for skin cancer development. UV light-induced DNA mutations in oncogenes and tumor suppressor genes promote the progression of AK to cSCC [6]

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