Comparative analysis of c-erbB-2 (HER-2/neu) in squamous cell carcinoma of the tongue: does over-expression exist? And what is its correlation with traditional diagnostic parameters?

Objectives:  Over‐expression of the proto‐oncogene c‐erbB‐2 (HER‐2/neu) has been shown to be a prognostic marker in many kinds of cancer, whereas conflicting data exist about the prevalence of HER‐2/neu over‐expression in squamous cell carcinoma (SCC) of the tongue. The status of Her‐2/neu was evalu...

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Veröffentlicht in:Journal of oral pathology & medicine 2008-03, Vol.37 (3), p.145-150
Hauptverfasser: Angiero, Francesca, Sordo, Rachele Del, Dessy, Enrico, Rossi, Elisa, Berenzi, Angiola, Stefani, Michele,  Sidoni, Angelo
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Sprache:eng
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Zusammenfassung:Objectives:  Over‐expression of the proto‐oncogene c‐erbB‐2 (HER‐2/neu) has been shown to be a prognostic marker in many kinds of cancer, whereas conflicting data exist about the prevalence of HER‐2/neu over‐expression in squamous cell carcinoma (SCC) of the tongue. The status of Her‐2/neu was evaluated in a series of SCC of the tongue to verify the frequency of over‐expression of HER‐2/neu and evaluate the correlation with traditional diagnostic parameters of this neoplasm. Method:  Fourty patients with SCC of the tongue were investigated for over‐expression of the protein through immunohistochemistry using CB11 antibody, the Hercep Test® kit and FISH. Results:  Data obtained using the Hercep Test® differ from published reports concerning the over‐expression of Her‐2/neu and there was no correlation between levels of expression of Her‐2/neu and other clinico‐pathological and/or prognostic parameters. Of the 40 specimens, using CB11 we obtained results in line with published reports; however, with the Hercep Test® we found only 1 positive case (2.5%) (score 3+). Conclusion:  These data, confirmed by FISH, suggest that Her‐2/neu is not a suitable marker that could play a primary role in the clinical‐therapeutic management of SCC of the tongue.
ISSN:0904-2512
1600-0714
DOI:10.1111/j.1600-0714.2007.00603.x