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Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma
Ion channels play a major factor in maintaining cellular homeostasis but very little is known about the role of these proteins in cancer biology. In this work we have discovered that, the Kv11.3 (hERG3) a plasma-membrane potassium channel plays a critical role in the regulation of autophagy in a can...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008339/ https://www.ncbi.nlm.nih.gov/pubmed/26942884 http://dx.doi.org/10.18632/oncotarget.7831 |
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author | Perez-Neut, Mathew Haar, Lauren Rao, Vidhya Santha, Sreevidya Lansu, Katherine Rana, Basabi Jones, Walter K. Gentile, Saverio |
author_facet | Perez-Neut, Mathew Haar, Lauren Rao, Vidhya Santha, Sreevidya Lansu, Katherine Rana, Basabi Jones, Walter K. Gentile, Saverio |
author_sort | Perez-Neut, Mathew |
collection | PubMed |
description | Ion channels play a major factor in maintaining cellular homeostasis but very little is known about the role of these proteins in cancer biology. In this work we have discovered that, the Kv11.3 (hERG3) a plasma-membrane potassium channel plays a critical role in the regulation of autophagy in a cancer cell model. We have found that pharmacologic stimulation of the Kv11.3 channel with a small molecule activator, NS1643 induced autophagy via activation of an AMPK-dependent signaling pathway in melanoma cell line. In addition, we have found that NS1643 produced a strong inhibition of cell proliferation by activating a cellular senescence program. Furthermore, inhibition of autophagy via siRNA targeting AMPK or treatment with hydroxychloroquine an autophagy inhibitor activates apoptosis in NS1643-treated cells. Thus, we propose that, Kv11.3 is a novel mediator of autophagy, autophagy can be a survival mechanism contributing to cellular senescence, and that use of a combinatorial pharmacologic approach of Kv11.3 activator with inhibitors of autophagy represents a novel therapeutic approach against melanoma. |
format | Online Article Text |
id | pubmed-5008339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-50083392016-09-12 Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma Perez-Neut, Mathew Haar, Lauren Rao, Vidhya Santha, Sreevidya Lansu, Katherine Rana, Basabi Jones, Walter K. Gentile, Saverio Oncotarget Research Paper Ion channels play a major factor in maintaining cellular homeostasis but very little is known about the role of these proteins in cancer biology. In this work we have discovered that, the Kv11.3 (hERG3) a plasma-membrane potassium channel plays a critical role in the regulation of autophagy in a cancer cell model. We have found that pharmacologic stimulation of the Kv11.3 channel with a small molecule activator, NS1643 induced autophagy via activation of an AMPK-dependent signaling pathway in melanoma cell line. In addition, we have found that NS1643 produced a strong inhibition of cell proliferation by activating a cellular senescence program. Furthermore, inhibition of autophagy via siRNA targeting AMPK or treatment with hydroxychloroquine an autophagy inhibitor activates apoptosis in NS1643-treated cells. Thus, we propose that, Kv11.3 is a novel mediator of autophagy, autophagy can be a survival mechanism contributing to cellular senescence, and that use of a combinatorial pharmacologic approach of Kv11.3 activator with inhibitors of autophagy represents a novel therapeutic approach against melanoma. Impact Journals LLC 2016-03-01 /pmc/articles/PMC5008339/ /pubmed/26942884 http://dx.doi.org/10.18632/oncotarget.7831 Text en Copyright: © 2016 Perez-Neut et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Perez-Neut, Mathew Haar, Lauren Rao, Vidhya Santha, Sreevidya Lansu, Katherine Rana, Basabi Jones, Walter K. Gentile, Saverio Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title | Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title_full | Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title_fullStr | Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title_full_unstemmed | Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title_short | Activation of hERG3 channel stimulates autophagy and promotes cellular senescence in melanoma |
title_sort | activation of herg3 channel stimulates autophagy and promotes cellular senescence in melanoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008339/ https://www.ncbi.nlm.nih.gov/pubmed/26942884 http://dx.doi.org/10.18632/oncotarget.7831 |
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