4.7 Article

High-risk human papillomavirus in non-melanoma skin lesions from renal allograft recipients and immunocompetent patients

Journal

BRITISH JOURNAL OF CANCER
Volume 104, Issue 8, Pages 1334-1341

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2011.95

Keywords

human papillomavirus; non-melanoma skin cancer; renal transplantation; immunosuppression; p16(INK4a)

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BACKGROUND: High-risk human papillomaviruses (HR-HPVs) can be detected in a proportion of non-melanoma skin cancers. Data on prevalence are inconclusive, but are essential to estimate the relevance of HR-HPV, particularly with regard to prophylactic HPV vaccines for skin cancer prevention. METHODS: High-risk human papillomavirus DNA was investigated in 140 non-melanoma skin lesions from 54 immunocompetent patients and 33 immunosuppressed renal allograft recipients. Expression of p16(INK4a), a marker for HR-HPV oncogene expression in the uterine cervix, and of p53 and pRB was evaluated immunohistochemically. RESULTS: The highest prevalence of HR-HPV was found in squamous cell cancer (SCC) (46.2% (6 out of 13) in immunosuppressed and 23.5% (4 out of 17) in immunocompetent patients). High-risk human papillomavirus positivity was accompanied by diffuse p16(INK4a) expression in most SCC (P<0.001) and basal cell cancers (P = 0.02), while almost all SCC in situ were p16(INK4a) positive irrespective of HR-HPV presence (P = 0.66). Diffuse p16(INK4a) expression was associated with lack of pRB expression (P = 0.001). p53 was strongly expressed in 40.0% (56 out of 140) of the lesions irrespective of HR-HPV presence. CONCLUSION: High-risk human papillomavirus can be detected in lesions of keratinised squamous epithelia. The association of HR-HPV with diffuse p16(INK4a) expression might indicate HR-HPV oncogene expression in a proportion of lesions. Overexpression of p53 suggests p53 pathway alterations in HR-HPV-positive and -negative lesions. British Journal of Cancer (2011) 104, 1334-1341. doi:10.1038/bjc.2011.95 www.bjcancer.com Published online 22 March 2011 (C) 2011 Cancer Research UK

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