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

Authors :
Reuschenbach, M.
Tran, T.
Faulstich, F.
Hartschuh, W.
Vinokurova, S.
Kloor, M.
Krautkrämer, E.
Zeier, M.
Von Knebel Doeberitz, M.
Sommerer, C.
Krautkrämer, E
Source :
British Journal of Cancer; 4/12/2011, Vol. 104 Issue 8, p1334-1341, 8p, 1 Color Photograph, 2 Diagrams, 3 Charts
Publication Year :
2011

Abstract

<bold>Background: </bold>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.<bold>Methods: </bold>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.<bold>Results: </bold>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.<bold>Conclusion: </bold>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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
104
Issue :
8
Database :
Complementary Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
59963046
Full Text :
https://doi.org/10.1038/bjc.2011.95