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Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations

The phosphatidylinositol 3-kinase (PI3K) pathway is involved in a myriad of cellular signalling pathways that regulate cell growth, metabolism, proliferation and survival. As a result, alterations in the PI3K pathway are frequently associated with human cancers. Indeed, PIK3CA—the gene encoding the...

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Autores principales: Mitchell, Camilla B., Phillips, Wayne A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523081/
https://www.ncbi.nlm.nih.gov/pubmed/31018529
http://dx.doi.org/10.3390/biom9040158
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author Mitchell, Camilla B.
Phillips, Wayne A.
author_facet Mitchell, Camilla B.
Phillips, Wayne A.
author_sort Mitchell, Camilla B.
collection PubMed
description The phosphatidylinositol 3-kinase (PI3K) pathway is involved in a myriad of cellular signalling pathways that regulate cell growth, metabolism, proliferation and survival. As a result, alterations in the PI3K pathway are frequently associated with human cancers. Indeed, PIK3CA—the gene encoding the p110α catalytic subunit of PI3K—is one of the most commonly mutated human oncogenes. PIK3CA mutations have also been implicated in non-malignant conditions including congenital overgrowth syndromes and vascular malformations. In order to study the role of PIK3CA mutations in driving tumorigenesis and tissue overgrowth and to test potential therapeutic interventions for these conditions, model systems are essential. In this review we discuss the various mouse models currently available for preclinical studies into the biological consequences and clinical significance of PIK3CA mutations.
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spelling pubmed-65230812019-06-03 Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations Mitchell, Camilla B. Phillips, Wayne A. Biomolecules Review The phosphatidylinositol 3-kinase (PI3K) pathway is involved in a myriad of cellular signalling pathways that regulate cell growth, metabolism, proliferation and survival. As a result, alterations in the PI3K pathway are frequently associated with human cancers. Indeed, PIK3CA—the gene encoding the p110α catalytic subunit of PI3K—is one of the most commonly mutated human oncogenes. PIK3CA mutations have also been implicated in non-malignant conditions including congenital overgrowth syndromes and vascular malformations. In order to study the role of PIK3CA mutations in driving tumorigenesis and tissue overgrowth and to test potential therapeutic interventions for these conditions, model systems are essential. In this review we discuss the various mouse models currently available for preclinical studies into the biological consequences and clinical significance of PIK3CA mutations. MDPI 2019-04-23 /pmc/articles/PMC6523081/ /pubmed/31018529 http://dx.doi.org/10.3390/biom9040158 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Mitchell, Camilla B.
Phillips, Wayne A.
Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title_full Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title_fullStr Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title_full_unstemmed Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title_short Mouse Models for Exploring the Biological Consequences and Clinical Significance of PIK3CA Mutations
title_sort mouse models for exploring the biological consequences and clinical significance of pik3ca mutations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523081/
https://www.ncbi.nlm.nih.gov/pubmed/31018529
http://dx.doi.org/10.3390/biom9040158
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