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Overexpression of the cytokine osteopontin identifies aggressive laryngeal squamous cell carcinomas and enhances carcinoma cell proliferation and invasiveness.

Articolo
Data di Pubblicazione:
2005
Abstract:
Purpose: Osteopontin is a secreted cytokine that binds to the cell surface CD44v6 receptor. We studied osteopontin and CD44v6 expression in laryngeal squamous cell carcinomas and correlated osteopontin expression levels with clinicopathologic tumor features. Experimental Design:We used immunohistochemistry, immunoblotting, and reverse transcription- PCR to study osteopontin expression in 58 laryngeal squamous cell carcinomas. Cultured squamous carcinoma cells were treated with exogenous osteopontin or with RNA interference to knockdown osteopontin expression. Results: Osteopontin expression was higher in all the invasive carcinomas than in patientmatched normalmucosa. Its expression levels were significantly correlated with tumor stage and grade and with the presence of lymph node and distant metastases. Osteopontin positivity was negatively correlated with overall survival (P = 0.03). Osteopontin expression was paralleled by intense cell surface reactivity for CD44v6.Treatment of squamous carcinoma cells with recombinant osteopontin sharply increased proliferation and Matrigel invasion in comparison with the untreated cells parallel to activation of the mitogen-activated protein kinase/extracellular signalregulated kinase kinase/mitogen-activated protein kinase signaling cascade. Osteopontin knockdown by RNA interference, anti-CD44 antibodies, and mitogen-activated protein kinase/ extracellular signal-regulated kinase kinase inhibition prevented these effects. Conclusions:These results identify osteopontin as amarker and a potential therapeutic target in cases of aggressive laryngeal squamous cell carcinomas.
Tipologia CRIS:
01.01 Articolo in rivista
Elenco autori:
Santoro, Massimo; Melillo, ROSA MARINA; Celetti, Angela; Castellone, MARIA DOMENICA
Autori di Ateneo:
CASTELLONE MARIA DOMENICA
CELETTI ANGELA
Link alla scheda completa:
https://iris.cnr.it/handle/20.500.14243/52055
Pubblicato in:
CLINICAL CANCER RESEARCH (PRINT)
Journal
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