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Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology
Wnt signalling is a fundamental pathway involved in embryonic development and adult tissue homeostasis. Mutations in the pathway frequently lead to developmental defects and cancer. As such, therapeutic intervention of this pathway has generated tremendous interest. Dickkopf‐1 (DKK1) is a secreted i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727329/ https://www.ncbi.nlm.nih.gov/pubmed/28574171 http://dx.doi.org/10.1111/bph.13894 |
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author | Kagey, Michael H He, Xi |
author_facet | Kagey, Michael H He, Xi |
author_sort | Kagey, Michael H |
collection | PubMed |
description | Wnt signalling is a fundamental pathway involved in embryonic development and adult tissue homeostasis. Mutations in the pathway frequently lead to developmental defects and cancer. As such, therapeutic intervention of this pathway has generated tremendous interest. Dickkopf‐1 (DKK1) is a secreted inhibitor of β‐catenin‐dependent Wnt signalling and was originally characterized as a tumour suppressor based on the prevailing view that Wnt signalling promotes cancer pathogenesis. However, DKK1 appears to increase tumour growth and metastasis in preclinical models and its elevated expression correlates with a poor prognosis in a range of cancers, indicating that DKK1 has more complex cellular and biological functions than originally appreciated. Here, we review current evidence for the cancer‐promoting activity of DKK1 and recent insights into the effects of DKK1 on signalling pathways in both cancer and immune cells. We discuss the rationale and promise of targeting DKK1 for oncology. LINKED ARTICLES: This article is part of a themed section on WNT Signalling: Mechanisms and Therapeutic Opportunities. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.24/issuetoc |
format | Online Article Text |
id | pubmed-5727329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57273292017-12-13 Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology Kagey, Michael H He, Xi Br J Pharmacol Themed Section: Review Articles Wnt signalling is a fundamental pathway involved in embryonic development and adult tissue homeostasis. Mutations in the pathway frequently lead to developmental defects and cancer. As such, therapeutic intervention of this pathway has generated tremendous interest. Dickkopf‐1 (DKK1) is a secreted inhibitor of β‐catenin‐dependent Wnt signalling and was originally characterized as a tumour suppressor based on the prevailing view that Wnt signalling promotes cancer pathogenesis. However, DKK1 appears to increase tumour growth and metastasis in preclinical models and its elevated expression correlates with a poor prognosis in a range of cancers, indicating that DKK1 has more complex cellular and biological functions than originally appreciated. Here, we review current evidence for the cancer‐promoting activity of DKK1 and recent insights into the effects of DKK1 on signalling pathways in both cancer and immune cells. We discuss the rationale and promise of targeting DKK1 for oncology. LINKED ARTICLES: This article is part of a themed section on WNT Signalling: Mechanisms and Therapeutic Opportunities. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v174.24/issuetoc John Wiley and Sons Inc. 2017-07-07 2017-12 /pmc/articles/PMC5727329/ /pubmed/28574171 http://dx.doi.org/10.1111/bph.13894 Text en © 2017 The Authors. British Journal of Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Themed Section: Review Articles Kagey, Michael H He, Xi Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title | Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title_full | Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title_fullStr | Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title_full_unstemmed | Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title_short | Rationale for targeting the Wnt signalling modulator Dickkopf‐1 for oncology |
title_sort | rationale for targeting the wnt signalling modulator dickkopf‐1 for oncology |
topic | Themed Section: Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727329/ https://www.ncbi.nlm.nih.gov/pubmed/28574171 http://dx.doi.org/10.1111/bph.13894 |
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