4.7 Article

Activation of the EGFR/ERK pathway in high-grade mucoepidermoid carcinomas of the salivary glands

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BRITISH JOURNAL OF CANCER
卷 103, 期 4, 页码 510-516

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NATURE PUBLISHING GROUP
DOI: 10.1038/sj.bjc.6605788

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mucoepidermoid carcinoma; salivary gland carcinoma; epidermal growth factor; EGFR; extracellular signal-regulated kinase; ERK1/2

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BACKGROUND: Mucoepidermoid carcinoma (MEC) shows differences in biological behaviour depending mainly on its histological grade. High-grade tumours usually have an aggressive biological course and they require additional oncological treatment after surgery. METHODS: In a series of 43 MECs of the salivary glands, we studied the epidermal growth factor receptor (EGFR) gene by using dual-colour chromogenic in situ hybridisation (CISH). Moreover, we assessed the protein expressions of the EGFR and the activated extracellular signal-regulated kinases (pERK1/2) by using immunohistochemistry. These results were correlated with the histological grade of the tumours and the outcome of the patients. RESULTS: The CISH study demonstrated a high-EGFR gene copy number, with balanced chromosome 7 polysomy, in 8 out of 11 high-grade MECs (72.7%), whereas 27 low-grade and 15 intermediate-grade tumours had a normal EGFR gene copy number (P<0.001). The EGFR gene gains correlated with disease-free interval (P=0.003) and overall survival of the patients (P=0.019). The EGFR protein expression had a significant correlation with the histological grade of the tumours but not with the outcome of the patients. The pERK1/2 expression correlated with histological grade of tumours (P<0.001), disease-free interval (P=0.004) and overall survival (P=0.001). CONCLUSIONS: The EGFR/ERK pathway is activated in high-grade MECs with aggressive behaviour. Patients with these tumours who require oncological treatment in addition to surgery could benefit from EGFR and mitogen-activated protein kinase pathway inhibitors. British Journal of Cancer (2010) 103, 510-516. doi:10.1038/sj.bjc.6605788 www.bjcancer.com Published online 27 July 2010 (C) 2010 Cancer Research UK

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