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miR-19a and SOCS-1 expression in the differential diagnosis of laryngeal (glottic) verrucous squamous cell carcinoma

Authors :
Chiara Bedin
Luciano Giacomelli
Stella Blandamura
Donato Nitti
Giancarlo Ottaviano
Rocco Cappellesso
Edoardo Stellini
Gino Marioni
Marco Agostini
Tommaso Cacco
Cosimo de Filippis
Andrea Lovato
Rosario Marchese-Ragona
Source :
Journal of clinical pathology. 69(5)
Publication Year :
2015

Abstract

BackgroundLaryngeal verrucous squamous cell carcinoma (VSCC) is a highly differentiated squamous cell carcinoma (SCC), the diagnosis of which can meet with many pitfalls: benign hyperplastic lesions and conventional SCC are the most important differential diagnoses. The microRNA miR-19a is overexpressed in many solid tumours and regulates the suppressor of cytokine signalling-1 (SOCS-1) expression.AimsThe main endpoints were to assess miR-19a and SOCS-1 expression in glottic VSCC, and the former's potential role in differentiating between glottic VSCC, conventional SCC and hyperplastic lesions.MethodsThe expression of MiR-19a (by reverse transcription and quantitative real-time PCR) and SOCS-1 (by immunohistochemistry, rabbit polyclonal anti-SOCS-1 antibody) was assessed in 11 consecutive cases of glottic VSCC, 20 of papillary hyperplasia and 42 cases of conventional SCC.ResultsMean miR-19a expression was significantly higher (p=0.000) in malignant glottic lesions (conventional SCC/VSCC) than in benign conditions. Significant differences in mean miR-19a expression also emerged between conventional SCC and papillary hyperplasia (p=0.000), and between conventional SCC and VSCC (p=0.03). miR-19a expression was not statistically associated with SOCS-1 immunoreactivity or immunostaining intensity in VSCC, conventional SCC or papillary hyperplasia.ConclusionsOur preliminary outcomes suggest the utility of miR-19a in the challenging differential diagnosis of laryngeal VSCC. Although miR-19a has been found to regulate SOCS-1 expression, this evidence was not confirmed by this investigation.

Details

ISSN :
14724146
Volume :
69
Issue :
5
Database :
OpenAIRE
Journal :
Journal of clinical pathology
Accession number :
edsair.doi.dedup.....d1a39cba1230500a6d532a7fa28a5dd9