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Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer

The Hedgehog signaling pathway is one of the fundamental pathways required for development and regulation of postnatal regeneration in a variety of tissues. The pathway has also been associated with cancers since the identification of a mutation in one of its components, PTCH, as the cause of Basal...

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Autores principales: Suchors, Chamey, Kim, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406872/
https://www.ncbi.nlm.nih.gov/pubmed/36010600
http://dx.doi.org/10.3390/cells11162523
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author Suchors, Chamey
Kim, James
author_facet Suchors, Chamey
Kim, James
author_sort Suchors, Chamey
collection PubMed
description The Hedgehog signaling pathway is one of the fundamental pathways required for development and regulation of postnatal regeneration in a variety of tissues. The pathway has also been associated with cancers since the identification of a mutation in one of its components, PTCH, as the cause of Basal Cell Nevus Syndrome, which is associated with several cancers. Our understanding of the pathway in tumorigenesis has expanded greatly since that initial discovery over two decades ago. The pathway has tumor-suppressive and oncogenic functions depending on the context of the cancer. Furthermore, noncanonical activation of GLI transcription factors has been reported in a number of tumor types. Here, we review the roles of canonical Hedgehog signaling pathway and noncanonical GLI activation in cancers, particularly epithelial cancers, and discuss an emerging concept of the distinct outcomes that these modes have on cancer initiation and progression.
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spelling pubmed-94068722022-08-26 Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer Suchors, Chamey Kim, James Cells Review The Hedgehog signaling pathway is one of the fundamental pathways required for development and regulation of postnatal regeneration in a variety of tissues. The pathway has also been associated with cancers since the identification of a mutation in one of its components, PTCH, as the cause of Basal Cell Nevus Syndrome, which is associated with several cancers. Our understanding of the pathway in tumorigenesis has expanded greatly since that initial discovery over two decades ago. The pathway has tumor-suppressive and oncogenic functions depending on the context of the cancer. Furthermore, noncanonical activation of GLI transcription factors has been reported in a number of tumor types. Here, we review the roles of canonical Hedgehog signaling pathway and noncanonical GLI activation in cancers, particularly epithelial cancers, and discuss an emerging concept of the distinct outcomes that these modes have on cancer initiation and progression. MDPI 2022-08-14 /pmc/articles/PMC9406872/ /pubmed/36010600 http://dx.doi.org/10.3390/cells11162523 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Suchors, Chamey
Kim, James
Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title_full Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title_fullStr Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title_full_unstemmed Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title_short Canonical Hedgehog Pathway and Noncanonical GLI Transcription Factor Activation in Cancer
title_sort canonical hedgehog pathway and noncanonical gli transcription factor activation in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406872/
https://www.ncbi.nlm.nih.gov/pubmed/36010600
http://dx.doi.org/10.3390/cells11162523
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