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Wnt signaling in cancer stem cells and colon cancer metastasis

Overactivation of Wnt signaling is a hallmark of colorectal cancer (CRC). The Wnt pathway is a key regulator of both the early and the later, more invasive, stages of CRC development. In the normal intestine and colon, Wnt signaling controls the homeostasis of intestinal stem cells (ISCs) that fuel,...

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Autores principales: Basu, Sayon, Haase, Gal, Ben-Ze'ev, Avri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841194/
https://www.ncbi.nlm.nih.gov/pubmed/27134739
http://dx.doi.org/10.12688/f1000research.7579.1
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author Basu, Sayon
Haase, Gal
Ben-Ze'ev, Avri
author_facet Basu, Sayon
Haase, Gal
Ben-Ze'ev, Avri
author_sort Basu, Sayon
collection PubMed
description Overactivation of Wnt signaling is a hallmark of colorectal cancer (CRC). The Wnt pathway is a key regulator of both the early and the later, more invasive, stages of CRC development. In the normal intestine and colon, Wnt signaling controls the homeostasis of intestinal stem cells (ISCs) that fuel, via proliferation, upward movement of progeny cells from the crypt bottom toward the villus and differentiation into all cell types that constitute the intestine. Studies in recent years suggested that cancer stem cells (CSCs), similar to ISCs of the crypts, consist of a small subpopulation of the tumor and are responsible for the initiation and progression of the disease. Although various ISC signature genes were also identified as CRC markers and some of these genes were even demonstrated to have a direct functional role in CRC development, the origin of CSCs and their contribution to cancer progression is still debated. Here, we describe studies supporting a relationship between Wnt-regulated CSCs and the progression of CRC.
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spelling pubmed-48411942016-04-29 Wnt signaling in cancer stem cells and colon cancer metastasis Basu, Sayon Haase, Gal Ben-Ze'ev, Avri F1000Res Review Overactivation of Wnt signaling is a hallmark of colorectal cancer (CRC). The Wnt pathway is a key regulator of both the early and the later, more invasive, stages of CRC development. In the normal intestine and colon, Wnt signaling controls the homeostasis of intestinal stem cells (ISCs) that fuel, via proliferation, upward movement of progeny cells from the crypt bottom toward the villus and differentiation into all cell types that constitute the intestine. Studies in recent years suggested that cancer stem cells (CSCs), similar to ISCs of the crypts, consist of a small subpopulation of the tumor and are responsible for the initiation and progression of the disease. Although various ISC signature genes were also identified as CRC markers and some of these genes were even demonstrated to have a direct functional role in CRC development, the origin of CSCs and their contribution to cancer progression is still debated. Here, we describe studies supporting a relationship between Wnt-regulated CSCs and the progression of CRC. F1000Research 2016-04-19 /pmc/articles/PMC4841194/ /pubmed/27134739 http://dx.doi.org/10.12688/f1000research.7579.1 Text en Copyright: © 2016 Basu S et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Basu, Sayon
Haase, Gal
Ben-Ze'ev, Avri
Wnt signaling in cancer stem cells and colon cancer metastasis
title Wnt signaling in cancer stem cells and colon cancer metastasis
title_full Wnt signaling in cancer stem cells and colon cancer metastasis
title_fullStr Wnt signaling in cancer stem cells and colon cancer metastasis
title_full_unstemmed Wnt signaling in cancer stem cells and colon cancer metastasis
title_short Wnt signaling in cancer stem cells and colon cancer metastasis
title_sort wnt signaling in cancer stem cells and colon cancer metastasis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841194/
https://www.ncbi.nlm.nih.gov/pubmed/27134739
http://dx.doi.org/10.12688/f1000research.7579.1
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