Cargando…

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Sun, Han, Luo, Liqun, Lal, Bachchu, Ma, Xinrong, Chen, Lieping, Hann, Christine L., Fulton, Amy M., Leahy, Daniel J., Laterra, John, Li, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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
_version_ 1782414260584841216
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
work_keys_str_mv AT sunhan amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT luoliqun amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT lalbachchu amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT maxinrong amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT chenlieping amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT hannchristinel amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT fultonamym amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT leahydanielj amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT laterrajohn amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT limin amonoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT sunhan monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT luoliqun monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT lalbachchu monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT maxinrong monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT chenlieping monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT hannchristinel monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT fultonamym monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT leahydanielj monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT laterrajohn monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis
AT limin monoclonalantibodyagainstkcnk9kchannelextracellulardomaininhibitstumourgrowthandmetastasis