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Erschienen in: Virchows Archiv 3/2015

01.09.2015 | Original Article

Dysregulation of the Rb pathway in recurrent pleomorphic adenoma of the salivary glands

verfasst von: Ana Amélia de Souza, Albina Altemani, Fabricio Passador-Santos, Cecilia Pedroso Turssi, Ney Soares de Araujo, Vera Cavalcanti de Araújo, Andresa Borges Soares

Erschienen in: Virchows Archiv | Ausgabe 3/2015

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Abstract

Pleomorphic adenoma (PA) is the most common salivary gland neoplasm, and while mostly benign, recurrences (RPA) and malignant transformation to carcinoma ex-PA (CXPA) do occur. Cell cycle proteins important in its tumorigenesis have been studied as markers for PA with a high risk of RPA or CXPA. The aim of the present study was to investigate cell cycle markers p-16, cyclin D1, CDK4, E2F, and retinoblastoma (Rb) in this context. Expression of p16, cyclin D1, E2F, CDK4, and Rb was studied by immunohistochemistry in 24 cases of PA, 21 of RPA, and 2 of CXPA. The presence of HPV was assessed by in situ hybridization. Immunostaining for p16 and cyclin D1 was negative or weakly positive in most cases of PA while strongly positive in the majority of RPA and both CXPA cases. Staining for Rb and CDK4 was either negative or weakly positive in PA, RPA, and CXPA. Expression of E2F was stronger in RPA and CXPA than in PA. Nuclear reactivity for HPV was not observed in any case. In conclusion, the strong staining for p16, cyclinD1, and E2F in RPA and CXPA, while weak or negative in PA, suggests that these proteins might be involved in recurrence and malignant transformation of PA.
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Metadaten
Titel
Dysregulation of the Rb pathway in recurrent pleomorphic adenoma of the salivary glands
verfasst von
Ana Amélia de Souza
Albina Altemani
Fabricio Passador-Santos
Cecilia Pedroso Turssi
Ney Soares de Araujo
Vera Cavalcanti de Araújo
Andresa Borges Soares
Publikationsdatum
01.09.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Virchows Archiv / Ausgabe 3/2015
Print ISSN: 0945-6317
Elektronische ISSN: 1432-2307
DOI
https://doi.org/10.1007/s00428-015-1804-x

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