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Hedgehog Signaling in Malignant Pleural Mesothelioma
Malignant pleural mesothelioma (MPM) is a cancer associated with exposure to asbestos fibers, which accumulate in the pleural space, damage tissue and stimulate regeneration. Hedgehog signaling is a pathway important during embryonic mesothelium development and is inactivated in adult mesothelium. T...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4584313/ https://www.ncbi.nlm.nih.gov/pubmed/26184317 http://dx.doi.org/10.3390/genes6030500 |
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author | Felley-Bosco, Emanuela Opitz, Isabelle Meerang, Mayura |
author_facet | Felley-Bosco, Emanuela Opitz, Isabelle Meerang, Mayura |
author_sort | Felley-Bosco, Emanuela |
collection | PubMed |
description | Malignant pleural mesothelioma (MPM) is a cancer associated with exposure to asbestos fibers, which accumulate in the pleural space, damage tissue and stimulate regeneration. Hedgehog signaling is a pathway important during embryonic mesothelium development and is inactivated in adult mesothelium. The pathway is reactivated in some MPM patients with poor clinical outcome, mainly mediated by the expression of the ligands. Nevertheless, mutations in components of the pathway have been observed in a few cases. Data from different MPM animal models and primary culture suggest that both autocrine and paracrine Hedgehog signaling are important to maintain tumor growth. Drugs inhibiting the pathway at the level of the smoothened receptor (Smo) or glioma-associated protein transcription factors (Gli) have been used mostly in experimental models. For clinical development, biomarkers are necessary for the selection of patients who can benefit from Hedgehog signaling inhibition. |
format | Online Article Text |
id | pubmed-4584313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-45843132015-10-05 Hedgehog Signaling in Malignant Pleural Mesothelioma Felley-Bosco, Emanuela Opitz, Isabelle Meerang, Mayura Genes (Basel) Review Malignant pleural mesothelioma (MPM) is a cancer associated with exposure to asbestos fibers, which accumulate in the pleural space, damage tissue and stimulate regeneration. Hedgehog signaling is a pathway important during embryonic mesothelium development and is inactivated in adult mesothelium. The pathway is reactivated in some MPM patients with poor clinical outcome, mainly mediated by the expression of the ligands. Nevertheless, mutations in components of the pathway have been observed in a few cases. Data from different MPM animal models and primary culture suggest that both autocrine and paracrine Hedgehog signaling are important to maintain tumor growth. Drugs inhibiting the pathway at the level of the smoothened receptor (Smo) or glioma-associated protein transcription factors (Gli) have been used mostly in experimental models. For clinical development, biomarkers are necessary for the selection of patients who can benefit from Hedgehog signaling inhibition. MDPI 2015-07-08 /pmc/articles/PMC4584313/ /pubmed/26184317 http://dx.doi.org/10.3390/genes6030500 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Felley-Bosco, Emanuela Opitz, Isabelle Meerang, Mayura Hedgehog Signaling in Malignant Pleural Mesothelioma |
title | Hedgehog Signaling in Malignant Pleural Mesothelioma |
title_full | Hedgehog Signaling in Malignant Pleural Mesothelioma |
title_fullStr | Hedgehog Signaling in Malignant Pleural Mesothelioma |
title_full_unstemmed | Hedgehog Signaling in Malignant Pleural Mesothelioma |
title_short | Hedgehog Signaling in Malignant Pleural Mesothelioma |
title_sort | hedgehog signaling in malignant pleural mesothelioma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4584313/ https://www.ncbi.nlm.nih.gov/pubmed/26184317 http://dx.doi.org/10.3390/genes6030500 |
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