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WNK pathways in cancer signaling networks

BACKGROUND: The with no lysine [K] (WNK) pathway consists of the structurally unique WNK kinases, their downstream target kinases, oxidative stress responsive (OSR)1 and SPS/Ste20-related proline-alanine-rich kinase (SPAK), and a multitude of OSR1/SPAK substrates including cation chloride cotranspor...

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Autores principales: Gallolu Kankanamalage, Sachith, Karra, Aroon S., Cobb, Melanie H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215617/
https://www.ncbi.nlm.nih.gov/pubmed/30390653
http://dx.doi.org/10.1186/s12964-018-0287-1
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author Gallolu Kankanamalage, Sachith
Karra, Aroon S.
Cobb, Melanie H.
author_facet Gallolu Kankanamalage, Sachith
Karra, Aroon S.
Cobb, Melanie H.
author_sort Gallolu Kankanamalage, Sachith
collection PubMed
description BACKGROUND: The with no lysine [K] (WNK) pathway consists of the structurally unique WNK kinases, their downstream target kinases, oxidative stress responsive (OSR)1 and SPS/Ste20-related proline-alanine-rich kinase (SPAK), and a multitude of OSR1/SPAK substrates including cation chloride cotransporters. MAIN BODY: While the best known functions of the WNK pathway is regulation of ion transport across cell membranes, WNK pathway components have been implicated in numerous human diseases. The goal of our review is to draw attention to how this pathway and its components exert influence on the progression of cancer, specifically by detailing WNK signaling intersections with major cell communication networks and processes. CONCLUSION: Here we describe how WNKs and associated proteins interact with and influence PI3K-AKT, TGF-β, and NF-κB signaling, as well as its unanticipated role in the regulation of angiogenesis.
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spelling pubmed-62156172018-11-08 WNK pathways in cancer signaling networks Gallolu Kankanamalage, Sachith Karra, Aroon S. Cobb, Melanie H. Cell Commun Signal Review BACKGROUND: The with no lysine [K] (WNK) pathway consists of the structurally unique WNK kinases, their downstream target kinases, oxidative stress responsive (OSR)1 and SPS/Ste20-related proline-alanine-rich kinase (SPAK), and a multitude of OSR1/SPAK substrates including cation chloride cotransporters. MAIN BODY: While the best known functions of the WNK pathway is regulation of ion transport across cell membranes, WNK pathway components have been implicated in numerous human diseases. The goal of our review is to draw attention to how this pathway and its components exert influence on the progression of cancer, specifically by detailing WNK signaling intersections with major cell communication networks and processes. CONCLUSION: Here we describe how WNKs and associated proteins interact with and influence PI3K-AKT, TGF-β, and NF-κB signaling, as well as its unanticipated role in the regulation of angiogenesis. BioMed Central 2018-11-03 /pmc/articles/PMC6215617/ /pubmed/30390653 http://dx.doi.org/10.1186/s12964-018-0287-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Gallolu Kankanamalage, Sachith
Karra, Aroon S.
Cobb, Melanie H.
WNK pathways in cancer signaling networks
title WNK pathways in cancer signaling networks
title_full WNK pathways in cancer signaling networks
title_fullStr WNK pathways in cancer signaling networks
title_full_unstemmed WNK pathways in cancer signaling networks
title_short WNK pathways in cancer signaling networks
title_sort wnk pathways in cancer signaling networks
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6215617/
https://www.ncbi.nlm.nih.gov/pubmed/30390653
http://dx.doi.org/10.1186/s12964-018-0287-1
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