Expression and clinical significance of the Kv3.4 potassium channel subunit in the development and progression of head and neck squamous cell carcinomas

The concept of ion channels as membrane therapeutic targets and diagnostic/prognostic biomarkers has attracted growing attention. We therefore investigated the expression pattern and clinical significance of the Kv3.4 potassium channel subunit during the development and progression of head and neck...

Full description

Saved in:
Bibliographic Details
Published inThe Journal of pathology Vol. 221; no. 4; pp. 402 - 410
Main Authors Menéndez, Sofía Tirados, Rodrigo, Juan P, Allonca, Eva, García-Carracedo, Darío, Álvarez-Alija, Gustavo, Casado-Zapico, Sara, Fresno, Manuel F, Rodríguez, Carmen, Suárez, Carlos, García-Pedrero, Juana M
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.08.2010
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The concept of ion channels as membrane therapeutic targets and diagnostic/prognostic biomarkers has attracted growing attention. We therefore investigated the expression pattern and clinical significance of the Kv3.4 potassium channel subunit during the development and progression of head and neck squamous cell carcinomas (HNSCCs). KCNC4 mRNA levels were determined by real-time RT-PCR in both HNSCC tissue specimens and derived cell lines. Kv3.4 protein expression was evaluated by immunohistochemistry in paraffin-embedded tissue specimens from 84 patients with laryngeal/pharyngeal squamous cell carcinomas and 67 patients with laryngeal dysplasias. Molecular alterations were correlated with clinicopathological parameters and patient outcome. Increased KCNC4 mRNA levels were found in 15 (54%) of 28 tumours, compared to the corresponding normal epithelia and varied mRNA levels were detected in 12 HNSCC-derived cell lines analysed. Increased Kv3.4 protein expression was observed in 34 (40%) of 84 carcinomas and also at early stages of HNSCC tumourigenesis. Thus, 35 (52%) of 67 laryngeal lesions displayed Kv3.4-positive staining in the dysplastic areas, whereas both stromal cells and normal adjacent epithelia exhibited negligible expression. No significant correlations were found between Kv3.4-positive expression in HNSCC and clinical data; however, Kv3.4 expression tended to diminish in advanced-stage tumours. Interestingly, patients carrying Kv3.4-positive dysplasias experienced a significantly higher laryngeal cancer incidence than did those with negative lesions (p = 0.0209). In addition, functional studies using HNSCC cells revealed that inhibition of Kv3.4 expression by siRNA leads to the inhibition of cell proliferation via selective cell cycle arrest at the G2/M phase without affecting apoptosis. Collectively, these data demonstrate for the first time that Kv3.4 expression is frequently increased during HNSCC tumourigenesis and correlated significantly with a higher cancer risk. Our findings support a role for Kv3.4 in malignant transformation and provide original evidence for the potential clinical utility of Kv3.4 expression as a biomarker for cancer risk assessment. Copyright © 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
Bibliography:http://dx.doi.org/10.1002/path.2722
ISCIII
Statement of author contributions STM conceived and carried out experiments; EA, DGC, GAA, and SCZ carried out experiments; MFF, CR, and CS analysed data; and JPR and JMGP conceived experiments, analysed data and were involved in writing the manuscript. All authors approved the final version of the manuscript
Fondo de Investigación Sanitaria - No. CP07/00032 to JMGP; No. 07/0777 to JPR
RTICC - No. RD06/0020/0034; No. RD06/0020/1042
ArticleID:PATH2722
ark:/67375/WNG-KGSRD9HQ-X
Supporting Information: Figure S1. Control experiment to test the specificity of Kv3.4 staining pattern using anti-Kv3.4 antibody blocked by exposure to the peptide antigen.Supporting Information: Legends Figure S1Supporting Information
FICYT - No. IB09-068 to JMGP
No conflicts of interest were declared.
Obra Social Cajastur-IUOPA
istex:0BDE83E62FE5B74DBE8F25379915BF3D77AB09A4
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-3417
1096-9896
DOI:10.1002/path.2722