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Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is a major cause of cancer death worldwide. HCC is usually asymptomatic at potential curative stages, and it has very poor prognosis if detected later. Thus, the identification of early biomarkers and novel therapies is essential to improve HCC patient survival. Ion ch...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036561/ https://www.ncbi.nlm.nih.gov/pubmed/27703327 http://dx.doi.org/10.2147/BTT.S87402 |
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author | Chávez-López, María de Guadalupe Zúñiga-García, Violeta Pérez-Carreón, Julio Isael Avalos-Fuentes, Arturo Escobar, Yesenia Camacho, Javier |
author_facet | Chávez-López, María de Guadalupe Zúñiga-García, Violeta Pérez-Carreón, Julio Isael Avalos-Fuentes, Arturo Escobar, Yesenia Camacho, Javier |
author_sort | Chávez-López, María de Guadalupe |
collection | PubMed |
description | Hepatocellular carcinoma (HCC) is a major cause of cancer death worldwide. HCC is usually asymptomatic at potential curative stages, and it has very poor prognosis if detected later. Thus, the identification of early biomarkers and novel therapies is essential to improve HCC patient survival. Ion channels have been proposed as potential tumor markers and therapeutic targets for several cancers including HCC. Especially, the ether à-go-go-1 (Eag1) voltage-gated potassium channel has been suggested as an early marker for HCC. Eag1 is overexpressed during HCC development from the cirrhotic and the preneoplastic lesions preceding HCC in a rat model. The channel is also overexpressed in human HCC. Astemizole has gained great interest as a potential anticancer drug because it targets several proteins involved in cancer including Eag1. Actually, in vivo studies have shown that astemizole may have clinical utility for HCC prevention and treatment. Here, we will review first some general aspects of HCC including the current biomarkers and therapies, and then we will focus on Eag1 channels as promising tools in the early diagnosis of HCC. |
format | Online Article Text |
id | pubmed-5036561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50365612016-10-04 Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma Chávez-López, María de Guadalupe Zúñiga-García, Violeta Pérez-Carreón, Julio Isael Avalos-Fuentes, Arturo Escobar, Yesenia Camacho, Javier Biologics Review Hepatocellular carcinoma (HCC) is a major cause of cancer death worldwide. HCC is usually asymptomatic at potential curative stages, and it has very poor prognosis if detected later. Thus, the identification of early biomarkers and novel therapies is essential to improve HCC patient survival. Ion channels have been proposed as potential tumor markers and therapeutic targets for several cancers including HCC. Especially, the ether à-go-go-1 (Eag1) voltage-gated potassium channel has been suggested as an early marker for HCC. Eag1 is overexpressed during HCC development from the cirrhotic and the preneoplastic lesions preceding HCC in a rat model. The channel is also overexpressed in human HCC. Astemizole has gained great interest as a potential anticancer drug because it targets several proteins involved in cancer including Eag1. Actually, in vivo studies have shown that astemizole may have clinical utility for HCC prevention and treatment. Here, we will review first some general aspects of HCC including the current biomarkers and therapies, and then we will focus on Eag1 channels as promising tools in the early diagnosis of HCC. Dove Medical Press 2016-09-20 /pmc/articles/PMC5036561/ /pubmed/27703327 http://dx.doi.org/10.2147/BTT.S87402 Text en © 2016 Chávez-López et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Chávez-López, María de Guadalupe Zúñiga-García, Violeta Pérez-Carreón, Julio Isael Avalos-Fuentes, Arturo Escobar, Yesenia Camacho, Javier Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title | Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title_full | Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title_fullStr | Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title_full_unstemmed | Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title_short | Eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
title_sort | eag1 channels as potential early-stage biomarkers of hepatocellular carcinoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036561/ https://www.ncbi.nlm.nih.gov/pubmed/27703327 http://dx.doi.org/10.2147/BTT.S87402 |
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