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A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis
Two-pore domain potassium (K2P) channels act to maintain cell resting membrane potential—a prerequisite for many biological processes. KCNK9, a member of K2P family, is implicated in cancer, owing to its overexpression in human tumours and its ability to promote neoplastic cell survival and growth....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742836/ https://www.ncbi.nlm.nih.gov/pubmed/26842342 http://dx.doi.org/10.1038/ncomms10339 |
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author | Sun, Han Luo, Liqun Lal, Bachchu Ma, Xinrong Chen, Lieping Hann, Christine L. Fulton, Amy M. Leahy, Daniel J. Laterra, John Li, Min |
author_facet | Sun, Han Luo, Liqun Lal, Bachchu Ma, Xinrong Chen, Lieping Hann, Christine L. Fulton, Amy M. Leahy, Daniel J. Laterra, John Li, Min |
author_sort | Sun, Han |
collection | PubMed |
description | Two-pore domain potassium (K2P) channels act to maintain cell resting membrane potential—a prerequisite for many biological processes. KCNK9, a member of K2P family, is implicated in cancer, owing to its overexpression in human tumours and its ability to promote neoplastic cell survival and growth. However, KCNK9's underlying contributions to malignancy remain elusive due to the absence of specific modulators. Here we describe the development of monoclonal antibodies against the KCNK9 extracellular domain and their functional effects. We show that one antibody (Y4) with the highest affinity binding induces channel internalization. The addition of Y4 to KCNK9-expressing carcinoma cells reduces cell viability and increases cell death. Systemic administration of Y4 effectively inhibits growth of human lung cancer xenografts and murine breast cancer metastasis in mice. Evidence for Y4-mediated carcinoma cell autonomous and immune-dependent cytotoxicity is presented. Our study reveals that antibody-based KCNK9 targeting is a promising therapeutic strategy in KCNK9-expressing malignancies. |
format | Online Article Text |
id | pubmed-4742836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47428362016-03-04 A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis Sun, Han Luo, Liqun Lal, Bachchu Ma, Xinrong Chen, Lieping Hann, Christine L. Fulton, Amy M. Leahy, Daniel J. Laterra, John Li, Min Nat Commun Article Two-pore domain potassium (K2P) channels act to maintain cell resting membrane potential—a prerequisite for many biological processes. KCNK9, a member of K2P family, is implicated in cancer, owing to its overexpression in human tumours and its ability to promote neoplastic cell survival and growth. However, KCNK9's underlying contributions to malignancy remain elusive due to the absence of specific modulators. Here we describe the development of monoclonal antibodies against the KCNK9 extracellular domain and their functional effects. We show that one antibody (Y4) with the highest affinity binding induces channel internalization. The addition of Y4 to KCNK9-expressing carcinoma cells reduces cell viability and increases cell death. Systemic administration of Y4 effectively inhibits growth of human lung cancer xenografts and murine breast cancer metastasis in mice. Evidence for Y4-mediated carcinoma cell autonomous and immune-dependent cytotoxicity is presented. Our study reveals that antibody-based KCNK9 targeting is a promising therapeutic strategy in KCNK9-expressing malignancies. Nature Publishing Group 2016-02-04 /pmc/articles/PMC4742836/ /pubmed/26842342 http://dx.doi.org/10.1038/ncomms10339 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sun, Han Luo, Liqun Lal, Bachchu Ma, Xinrong Chen, Lieping Hann, Christine L. Fulton, Amy M. Leahy, Daniel J. Laterra, John Li, Min A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title | A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title_full | A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title_fullStr | A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title_full_unstemmed | A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title_short | A monoclonal antibody against KCNK9 K(+) channel extracellular domain inhibits tumour growth and metastasis |
title_sort | monoclonal antibody against kcnk9 k(+) channel extracellular domain inhibits tumour growth and metastasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742836/ https://www.ncbi.nlm.nih.gov/pubmed/26842342 http://dx.doi.org/10.1038/ncomms10339 |
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