Scientists uncover potential mechanism for HPV-induced skin cancer

Scientists uncover potential mechanism for HPV-induced skin cancer
C/EBPα and miR 203 expression in non-lesional and HPV8-positive lesional skin of Epidermodysplasia verruciformis patients. Sections of non-lesional skin (upper and lower left) and HPV8-positive lesional skin (upper and lower right) from EV-patients were stained in red using antibodies against C/EBPα (upper left and right) and in blue by in situ hybridization with a probe against miR-203 (lower left and right). Nuclear counterstaining was performed with hematoxylin solution (upper left and right). Credit: Marthaler AM, et al. (2017)

Scientists have identified a molecular pathway by which some types of human papilloma virus (HPV) might increase the risk of skin cancer, particularly in people with the rare genetic disorder epidermodysplasia verruciformis (EV). The novel pathway is described in PLOS Pathogens.

Some HPV types of the genus known as beta-HPV infect cells and can increase the risk of non-melanoma , especially in people with weakened immune systems or EV. Previous research has suggested that a type of HPV protein called E6 underlies this increased cancer risk, but the molecular mechanisms by which E6 proteins may act are unclear.

To better understand the role of E6 proteins in skin cancer, a team led by Sigrun Smola, professor and chair of the Institute of Virology, Saarland University, Germany, focused on HPV infection in EV patients. EV makes people particularly vulnerable to infection with beta-HPV strains, so the disease provides a useful opportunity to study beta-HPV infection mechanisms.

The research team obtained samples of skin lesions from EV patients; some of these lesions tested positive for infection with HPV8, a type of beta-HPV. Molecular analysis revealed that the HPV8-infected lesions expressed significantly lower levels of microRNA-203, a known regulator of skin cell growth and differentiation. The HPV8-infected lesions also had higher levels of p63, a protein that is regulated by microRNA-203 and has been associated with cancer development.

Lab experiments with human skin cells performed predominantly by Anna Marthaler, PhD, then revealed molecular links between these microRNA-203/p63 effects and HPV8 infection. The results suggested that HPV8's E6 protein suppresses expression of C/EBPα, a protein that is known to play a key role in curbing the development of sun-induced skin cancer.

Additional analysis showed that C/EBPα directly regulates microRNA-203 and is in turn regulated by the protein p300, a known target of E6 proteins. The researchers also showed that HPV8-infected skin lesions from EV patients had significantly lower levels of C/EBPα and microRNA-203 than did non-lesional .

Overall, these findings suggest the existence of a previously unknown molecular pathway involving p300, C/EBPα, and microRNA-203 that helps to maintain normal skin cell proliferation and differentiation. HPV8's E6 appears to disturb the normal function of this pathway in EV patients, potentially paving the way for skin cancer.

"Our findings are particularly exciting because we now better understand how beta-HPV infection can contribute to UV-induced skin carcinogenesis," the authors explain. "This discovery opens new avenues for therapeutic interventions against skin cancer."


Explore further

A new unexpected key player in melanoma development identified

More information: Marthaler AM, Podgorska M, Feld P, Fingerle A, Knerr-Rupp K, Grässer F, et al. (2017) Identification of C/EBPα as a novel target of the HPV8 E6 protein regulating miR-203 in human keratinocytes. PLoS Pathog 13(6): e1006406. doi.org/10.1371/journal.ppat.1006406
Provided by Public Library of Science
Citation: Scientists uncover potential mechanism for HPV-induced skin cancer (2017, June 22) retrieved 22 March 2019 from https://medicalxpress.com/news/2017-06-scientists-uncover-potential-mechanism-hpv-induced.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.
0 shares

Feedback to editors

User comments

Please sign in to add a comment. Registration is free, and takes less than a minute. Read more