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Wnt and Kras signaling-dark siblings in lung cancer

Aberrant Kras signaling is observed in a high percentage of human lung cancers while activating mutations in the Wnt/β-catenin signaling pathway are only rarely found. Our recent work has shown that the combined activation of both Kras and Wnt/β-catenin signaling leads to a dramatic increase in both...

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Detalles Bibliográficos
Autores principales: Pacheco-Pinedo, Eugenia C., Morrisey, Edward E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248175/
https://www.ncbi.nlm.nih.gov/pubmed/21753228
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author Pacheco-Pinedo, Eugenia C.
Morrisey, Edward E.
author_facet Pacheco-Pinedo, Eugenia C.
Morrisey, Edward E.
author_sort Pacheco-Pinedo, Eugenia C.
collection PubMed
description Aberrant Kras signaling is observed in a high percentage of human lung cancers while activating mutations in the Wnt/β-catenin signaling pathway are only rarely found. Our recent work has shown that the combined activation of both Kras and Wnt/β-catenin signaling leads to a dramatic increase in both tumor incidence and size. Moreover, lung tumors generated by the combined activation of both of these pathways exhibit a distinct phenotype similar to embryonic progenitors found in the developing lung. Thus, combinatorial activation of Kras and Wnt/β-catenin pathways leads to a significant increase in lung tumor formation characterized by a more progenitor like phenotype.
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spelling pubmed-32481752012-01-18 Wnt and Kras signaling-dark siblings in lung cancer Pacheco-Pinedo, Eugenia C. Morrisey, Edward E. Oncotarget Research Perspectives Aberrant Kras signaling is observed in a high percentage of human lung cancers while activating mutations in the Wnt/β-catenin signaling pathway are only rarely found. Our recent work has shown that the combined activation of both Kras and Wnt/β-catenin signaling leads to a dramatic increase in both tumor incidence and size. Moreover, lung tumors generated by the combined activation of both of these pathways exhibit a distinct phenotype similar to embryonic progenitors found in the developing lung. Thus, combinatorial activation of Kras and Wnt/β-catenin pathways leads to a significant increase in lung tumor formation characterized by a more progenitor like phenotype. Impact Journals LLC 2011-07-13 /pmc/articles/PMC3248175/ /pubmed/21753228 Text en Copyright: © 2011 Pacheco-Pinedo and Morrisey 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 Research Perspectives
Pacheco-Pinedo, Eugenia C.
Morrisey, Edward E.
Wnt and Kras signaling-dark siblings in lung cancer
title Wnt and Kras signaling-dark siblings in lung cancer
title_full Wnt and Kras signaling-dark siblings in lung cancer
title_fullStr Wnt and Kras signaling-dark siblings in lung cancer
title_full_unstemmed Wnt and Kras signaling-dark siblings in lung cancer
title_short Wnt and Kras signaling-dark siblings in lung cancer
title_sort wnt and kras signaling-dark siblings in lung cancer
topic Research Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3248175/
https://www.ncbi.nlm.nih.gov/pubmed/21753228
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