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Maspin expression and melanoma progression: a matter of sub-cellular localization.
Martinoli, Chiara; Gandini, Sara; Luise, Chiara; Mazzarol, Giovanni; Confalonieri, Stefano; Giuseppe Pelicci, Pier; Testori, Alessandro; Ferrucci, Pier Francesco.
Afiliação
  • Martinoli C; Medical Oncology of Melanoma Unit, Division of Medical Oncology, European Institute of Oncology, Milan, Italy.
  • Gandini S; Division of Statistics and Epidemiology, European Institute of Oncology, Milan, Italy.
  • Luise C; Molecular Medicine for Care Program, European Institute of Oncology, Milan, Italy.
  • Mazzarol G; Molecular Medicine for Care Program, European Institute of Oncology, Milan, Italy.
  • Confalonieri S; Molecular Medicine for Care Program, European Institute of Oncology, Milan, Italy.
  • Giuseppe Pelicci P; Department of Experimental Oncology, European Institute of Oncology, Milan, Italy.
  • Testori A; Division of Melanoma and Soft Tissue Sarcomas, European Institute of Oncology, Milan, Italy.
  • Ferrucci PF; Medical Oncology of Melanoma Unit, Division of Medical Oncology, European Institute of Oncology, Milan, Italy.
Mod Pathol ; 27(3): 412-9, 2014 Mar.
Article em En | MEDLINE | ID: mdl-24030740
Maspin, a member of the serpin family of protease inhibitors, is involved in key processes of cancer progression. Its biological activity seems to be cancer and compartment specific, with the protein acting either as a suppressor or as a tumor promoter in different cancer types. Characterization of maspin expression and its sub-cellular localization in melanoma is missing, hence, we aim to investigate its possible association with melanoma prognostic factors and disease progression. Nuclear and cytoplasmic maspin expression were evaluated on 60 nevi, 152 primary lesions, and 106 melanoma metastases using tissue microarrays and immunohistochemistry. The association between maspin immunoreactivity and patient's clinic-pathological features was evaluated. Multivariate logistic models and survival analyses were performed for maspin expression in primary melanomas. Nuclear maspin was detected in 8% nevi, 49% primary melanomas, and 28% metastases, whereas cytoplasmic maspin in 12% nevi, 18% primary lesions, and 9% metastases. In univariate analysis, nuclear maspin expression in primary melanomas was significantly associated with melanoma prognostic factors (nodular histotype, tumor thickness, mitotic rate, and ulceration) and disease stage, whereas cytoplasmic maspin was observed at higher frequency in thin superficial spreading melanomas, without mitosis. In multivariate analysis, nuclear maspin remained significantly associated with risk of developing a tumor prone to disease progression and, accordingly, with significantly shorter disease-free and overall survival. In this study, maspin was expressed at highest frequency in primary lesions and when expressed in the nuclei, was significantly associated with poor prognostic markers, melanoma recurrence, and worse survival. The present study suggests a tumor-suppressive effect of cytoplasmic maspin and a tumor-promoting effect of nuclear maspin, which open the discussion on its potential use in cancer therapy.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Biomarcadores Tumorais / Serpinas / Melanoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Biomarcadores Tumorais / Serpinas / Melanoma Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Itália