| Literature DB >> 25462861 |
Elgar S Quabius1, Tibor Görögh2, Gerrit S Fischer2, Anna S Hoffmann3, Maximilian Gebhard4, Matthias Evert5, Achim Beule6, Steffen Maune7, Rainald Knecht8, Attila Óvári9, Martin Durisin10, Florian Hoppe11, Christoph Röcken12, Jürgen Hedderich13, Petra Ambrosch2, Markus Hoffmann14.
Abstract
Recently, we demonstrated a significant inverse correlation between HPV-infection and SLPI-expression suggesting that SLPI protects against HPV-infection of HNSCC. Here we analyzed in a single lab setting 307 formalin-fixed paraffin-embedded HNSCC cases (tonsillar n = 135; non-tonsillar: n = 172) from eight health care centers. Samples were analyzed for SLPI gene- and protein-expression. Annexin A2, its heterotetramer A2t, putatively facilitating HPV- and SLPI-cell entry, was measured to study the correlation between SLPI and annexin A2. Data were correlated with tobacco consumption and HPV-status. Overall, HPV-DNA prevalence was 23.5% (72/307); attributed to: 43.7% (59/135) tonsillar and 7.6% (13/172) non-tonsillar cases. Smoking resulted in 6.44-fold increased and HPV-infection in 3.46-fold decreased SLPI-gene expression in all HNSCC with similar significant results obtained in tonsillar and non-tonsillar SCC separately. Correlating annexin A2- and SLPI-gene expression showed a significant surplus of annexin A2 in HPV-positive tumors (4.21× more annexin A2) and 6.72× more annexin A2 than SLPI in nonsmokers in all HNSCCs and similar significant results for both tumor entities separately. The surplus of annexin A2 in non-smokers and HPV-positive patients supports our hypothesis that decreased SLPI levels facilitate HPV-infection i.e., increased SLPI-expression may protect against HPV-infection of tonsillar and non-tonsillar SCC.Entities:
Keywords: Annexin A2; HNSCC; HPV; SLPI
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Year: 2014 PMID: 25462861 DOI: 10.1016/j.canlet.2014.11.043
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679