Log on / register
BioMed Central home | Journals A-Z | Feedback | Support | My details
Open AccessResearch

Ether à go-go potassium channel expression in soft tissue sarcoma patients

Fernanda Mello de Queiroz1,2 email, Guilherme Suarez-Kurtz1 email, Walter Stühmer2 email and Luis A Pardo2 email

Divisão de Farmacologia, Coordenação de Pesquisa, Instituto Nacional do Câncer, Rua André Cavalcanti 37/3° andar, Rio de Janeiro, Brazil

Max-Planck-Institut für Experimentelle Medizin Hermann-Rein-Str. 3, 37075 Göttingen, Germany

author email corresponding author email

Molecular Cancer 2006, 5:42doi:10.1186/1476-4598-5-42

Published: 5 October 2006

Abstract

Background

The expression of the human Eag1 potassium channel (Kv10.1) is normally restricted to the adult brain, but it has been detected in both tumour cell lines and primary tumours. Our purpose was to determine the frequency of expression of Eag1 in soft tissue sarcoma and its potential clinical implications.

Results

We used specific monoclonal antibodies to determine the expression levels of Eag1 in soft tissue sarcomas from 210 patients by immunohistochemistry. Eag1 was expressed in 71% of all tumours, with frequencies ranging from 56% (liposarcoma) to 82% (rhabdomyosarcoma). We detected differences in expression levels depending on the histological type, but no association was seen between expression of this protein and sex, age, grade or tumour size. Four cell lines derived from relevant sarcoma histological types (fibrosarcoma and rhabdomyosarcoma) were tested for Eag1 expression by real-time RT-PCR. We found all four lines to be positive for Eag1. In these cell lines, blockage of Eag1 by RNA interference led to a decrease in proliferation.

Conclusion

Eag1 is aberrantly expressed in over 70% sarcomas. In sarcoma cell lines, inhibition of Eag1 expression and/or function leads to reduced proliferation. The high frequency of expression of Eag1 in primary tumours and the restriction of normal expression of the channel to the brain, suggests the application of this protein for diagnostic or therapeutic purposes.


© 1999-2010 BioMed Central Ltd unless otherwise stated. Part of Springer Science+Business Media.