We analyzed survivin as a marker of cervical intraepithelial neoplasia (CIN) and high-risk human papillomavirus (HR-HPV) and a predictor of HPV clearance and disease outcome in cervical cancer in 302 samples (squamous cell carcinomas [SCCs], 150; CIN lesions, 152) by immunohistochemical staining with survivin antibody and HPV testing using polymerase chain reaction. HR-HPV types were associated closely with CIN and SCC. There was a significant linear relationship between grade and intensity of survivin expression (P = .0001). Survivin overexpression also was associated strongly with HR-HPV type (P = .0001). Multivariate regression analysis revealed survivin and p16(INK4a) as equally strong independent predictors of HR-HPV. Deregulated survivin expression did not predict clearance or persistence of HR-HPV after treatment of CIN or survival in cervical cancer in univariate (P = .417) or multivariate analysis. After adjustment for HR-HPV, stage, age, and tumor grade in the Cox regression model, only stage (P = .0001) and age (P = .0001) remained independent prognostic predictors. Survivin seems to be an early marker of cervical carcinogenesis. Up-regulated survivin expression was an independent predictor of HR-HPV in cervical lesions, most plausibly explained by its normal transcriptional repression by wild-type p53 being eliminated by HR-HPV E6 oncoprotein.

Branca, M., Giorgi, C., Santini, D., Di Bonito, L., Ciotti, M., Costa, S., et al. (2005). Survivin as a marker of cervical intraepithelial neoplasia and high-risk human papillomavirus and a predictor of virus clearance and prognosis in cervical cancer. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 124(1), 113-121 [10.1309/L8BWF431WU9AC8FJ].

Survivin as a marker of cervical intraepithelial neoplasia and high-risk human papillomavirus and a predictor of virus clearance and prognosis in cervical cancer

COSTA, STEFANO;FAVALLI, CARTESIO;
2005-07-01

Abstract

We analyzed survivin as a marker of cervical intraepithelial neoplasia (CIN) and high-risk human papillomavirus (HR-HPV) and a predictor of HPV clearance and disease outcome in cervical cancer in 302 samples (squamous cell carcinomas [SCCs], 150; CIN lesions, 152) by immunohistochemical staining with survivin antibody and HPV testing using polymerase chain reaction. HR-HPV types were associated closely with CIN and SCC. There was a significant linear relationship between grade and intensity of survivin expression (P = .0001). Survivin overexpression also was associated strongly with HR-HPV type (P = .0001). Multivariate regression analysis revealed survivin and p16(INK4a) as equally strong independent predictors of HR-HPV. Deregulated survivin expression did not predict clearance or persistence of HR-HPV after treatment of CIN or survival in cervical cancer in univariate (P = .417) or multivariate analysis. After adjustment for HR-HPV, stage, age, and tumor grade in the Cox regression model, only stage (P = .0001) and age (P = .0001) remained independent prognostic predictors. Survivin seems to be an early marker of cervical carcinogenesis. Up-regulated survivin expression was an independent predictor of HR-HPV in cervical lesions, most plausibly explained by its normal transcriptional repression by wild-type p53 being eliminated by HR-HPV E6 oncoprotein.
lug-2005
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/07 - MICROBIOLOGIA E MICROBIOLOGIA CLINICA
English
Con Impact Factor ISI
Microtubule-Associated Proteins; Humans; Prognosis; Papillomaviridae; Inhibitor of Apoptosis Proteins; Cervical Intraepithelial Neoplasia; Uterine Cervical Neoplasms; Cyclin-Dependent Kinase Inhibitor p16; Polymerase Chain Reaction; Neoplasm Proteins; Papillomavirus Infections; Carcinoma, Squamous Cell; Tumor Markers, Biological; Immunohistochemistry; Female
Branca, M., Giorgi, C., Santini, D., Di Bonito, L., Ciotti, M., Costa, S., et al. (2005). Survivin as a marker of cervical intraepithelial neoplasia and high-risk human papillomavirus and a predictor of virus clearance and prognosis in cervical cancer. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 124(1), 113-121 [10.1309/L8BWF431WU9AC8FJ].
Branca, M; Giorgi, C; Santini, D; Di Bonito, L; Ciotti, M; Costa, S; Benedetto, A; Casolati, E; Favalli, C; Paba, P; Di Bonito, P; Mariani, L; Syrjänen, S; Bonifacio, D; Accardi, L; Zanconati, F; Syrjänen, K
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/31072
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