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Current views on the role of Notch signaling and the pathogenesis of human leukemia

The Notch signaling pathway is highly conserved from Drosophila to humans and plays an important role in the regulation of cellular proliferation, differentiation and apoptosis. Constitutive activation of Notch signaling has been shown to result in excessive cellular proliferation and a wide range o...

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Detalles Bibliográficos
Autores principales: Pancewicz, Joanna, Nicot, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262490/
https://www.ncbi.nlm.nih.gov/pubmed/22128846
http://dx.doi.org/10.1186/1471-2407-11-502
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author Pancewicz, Joanna
Nicot, Christophe
author_facet Pancewicz, Joanna
Nicot, Christophe
author_sort Pancewicz, Joanna
collection PubMed
description The Notch signaling pathway is highly conserved from Drosophila to humans and plays an important role in the regulation of cellular proliferation, differentiation and apoptosis. Constitutive activation of Notch signaling has been shown to result in excessive cellular proliferation and a wide range of malignancies, including leukemia, glioblastoma and lung and breast cancers. Notch can also act as a tumor suppressor, and its inactivation has been associated with an increased risk of spontaneous squamous cell carcinoma. This minireview focuses on recent advances related to the mechanisms and roles of activated Notch1, Notch2, Notch3 and Notch4 signaling in human lymphocytic leukemia, myeloid leukemia and B cell lymphoma, as well as their significance, and recent advances in Notch-targeted therapies.
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spelling pubmed-32624902012-01-21 Current views on the role of Notch signaling and the pathogenesis of human leukemia Pancewicz, Joanna Nicot, Christophe BMC Cancer Review The Notch signaling pathway is highly conserved from Drosophila to humans and plays an important role in the regulation of cellular proliferation, differentiation and apoptosis. Constitutive activation of Notch signaling has been shown to result in excessive cellular proliferation and a wide range of malignancies, including leukemia, glioblastoma and lung and breast cancers. Notch can also act as a tumor suppressor, and its inactivation has been associated with an increased risk of spontaneous squamous cell carcinoma. This minireview focuses on recent advances related to the mechanisms and roles of activated Notch1, Notch2, Notch3 and Notch4 signaling in human lymphocytic leukemia, myeloid leukemia and B cell lymphoma, as well as their significance, and recent advances in Notch-targeted therapies. BioMed Central 2011-11-30 /pmc/articles/PMC3262490/ /pubmed/22128846 http://dx.doi.org/10.1186/1471-2407-11-502 Text en Copyright ©2011 Pancewicz and Nicot; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Pancewicz, Joanna
Nicot, Christophe
Current views on the role of Notch signaling and the pathogenesis of human leukemia
title Current views on the role of Notch signaling and the pathogenesis of human leukemia
title_full Current views on the role of Notch signaling and the pathogenesis of human leukemia
title_fullStr Current views on the role of Notch signaling and the pathogenesis of human leukemia
title_full_unstemmed Current views on the role of Notch signaling and the pathogenesis of human leukemia
title_short Current views on the role of Notch signaling and the pathogenesis of human leukemia
title_sort current views on the role of notch signaling and the pathogenesis of human leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3262490/
https://www.ncbi.nlm.nih.gov/pubmed/22128846
http://dx.doi.org/10.1186/1471-2407-11-502
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