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Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells

Cancer stem cells (CSCs) represent a unique subset of cells within a tumor that possess self-renewal capacity and pluripotency, and can drive tumor initiation and maintenance. First identified in hematological malignancies, CSCs are now thought to play an important role in a wide variety of solid tu...

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Detalles Bibliográficos
Autores principales: Curtin, Joshua C., Lorenzi, Matthew V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248130/
https://www.ncbi.nlm.nih.gov/pubmed/21317452
http://dx.doi.org/10.18632/oncotarget.191
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author Curtin, Joshua C.
Lorenzi, Matthew V.
author_facet Curtin, Joshua C.
Lorenzi, Matthew V.
author_sort Curtin, Joshua C.
collection PubMed
description Cancer stem cells (CSCs) represent a unique subset of cells within a tumor that possess self-renewal capacity and pluripotency, and can drive tumor initiation and maintenance. First identified in hematological malignancies, CSCs are now thought to play an important role in a wide variety of solid tumors such as NSCLC, breast and colorectal cancer. The role of CSCs in driving tumor formation illustrates the dysregulation of differentiation in tumorigenesis. The Wnt, Notch and Hedgehog (HH) pathways are developmental pathways that are commonly activated in many types of cancer. While substantial progress has been made in developing therapeutics targeting Notch and HH, the Wnt pathway has remained an elusive therapeutic target. This review will focus on the clinical relevance of the Wnt pathway in CSCs and tumor cell biology, as well as points of therapeutic intervention and recent advances in targeting Wnt/β-catenin signaling.
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spelling pubmed-32481302011-05-01 Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells Curtin, Joshua C. Lorenzi, Matthew V. Oncotarget Reviews Cancer stem cells (CSCs) represent a unique subset of cells within a tumor that possess self-renewal capacity and pluripotency, and can drive tumor initiation and maintenance. First identified in hematological malignancies, CSCs are now thought to play an important role in a wide variety of solid tumors such as NSCLC, breast and colorectal cancer. The role of CSCs in driving tumor formation illustrates the dysregulation of differentiation in tumorigenesis. The Wnt, Notch and Hedgehog (HH) pathways are developmental pathways that are commonly activated in many types of cancer. While substantial progress has been made in developing therapeutics targeting Notch and HH, the Wnt pathway has remained an elusive therapeutic target. This review will focus on the clinical relevance of the Wnt pathway in CSCs and tumor cell biology, as well as points of therapeutic intervention and recent advances in targeting Wnt/β-catenin signaling. Impact Journals LLC 2010-10-30 /pmc/articles/PMC3248130/ /pubmed/21317452 http://dx.doi.org/10.18632/oncotarget.191 Text en Copyright: © 2010 Curtin and Lorenzi http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Reviews
Curtin, Joshua C.
Lorenzi, Matthew V.
Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title_full Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title_fullStr Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title_full_unstemmed Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title_short Drug Discovery Approaches to Target Wnt Signaling in Cancer Stem Cells
title_sort drug discovery approaches to target wnt signaling in cancer stem cells
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248130/
https://www.ncbi.nlm.nih.gov/pubmed/21317452
http://dx.doi.org/10.18632/oncotarget.191
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