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Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors

Colorectal cancer is a major health problem and the second cause of cancer related death in western countries. Signaling pathways that control tissue homeostasis are often deregulated during tumorigenesis and contribute to tumor development. Studies in mouse models have shown that the p38 MAPK pathw...

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Autores principales: Gupta, Jalaj, Igea, Ana, Papaioannou, Marilena, Lopez-Casas, Pedro Pablo, Llonch, Elisabet, Hidalgo, Manuel, Gorgoulis, Vassilis G., Nebreda, Angel R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496165/
https://www.ncbi.nlm.nih.gov/pubmed/25890501
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author Gupta, Jalaj
Igea, Ana
Papaioannou, Marilena
Lopez-Casas, Pedro Pablo
Llonch, Elisabet
Hidalgo, Manuel
Gorgoulis, Vassilis G.
Nebreda, Angel R.
author_facet Gupta, Jalaj
Igea, Ana
Papaioannou, Marilena
Lopez-Casas, Pedro Pablo
Llonch, Elisabet
Hidalgo, Manuel
Gorgoulis, Vassilis G.
Nebreda, Angel R.
author_sort Gupta, Jalaj
collection PubMed
description Colorectal cancer is a major health problem and the second cause of cancer related death in western countries. Signaling pathways that control tissue homeostasis are often deregulated during tumorigenesis and contribute to tumor development. Studies in mouse models have shown that the p38 MAPK pathway regulates homeostasis in colon epithelial cells but also plays an important role in colon tumor maintenance. In this study, we have investigated the role of p38 MAPK signaling in patient-derived xenografts (PDXs) from three different human colon tumors representing clinical heterogeneity and that recapitulate the human tumor conditions both at histological and molecular levels. We have found that PH797804, a chemical inhibitor of p38 MAPK, reduces tumor growth of the three PDXs, which correlates with impaired colon tumor cell proliferation and survival. The inhibition of p38 MAPK in PDXs results in downregulation of the IL-6/STAT3 signaling pathway, which is a key regulator of colon tumorigenesis. Our results show the importance of p38 MAPK in human colon tumor growth using a preclinical model, and support that inhibition of p38 MAPK signaling may have therapeutic interest for colon cancer treatment.
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spelling pubmed-44961652015-07-10 Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors Gupta, Jalaj Igea, Ana Papaioannou, Marilena Lopez-Casas, Pedro Pablo Llonch, Elisabet Hidalgo, Manuel Gorgoulis, Vassilis G. Nebreda, Angel R. Oncotarget Priority Research Paper Colorectal cancer is a major health problem and the second cause of cancer related death in western countries. Signaling pathways that control tissue homeostasis are often deregulated during tumorigenesis and contribute to tumor development. Studies in mouse models have shown that the p38 MAPK pathway regulates homeostasis in colon epithelial cells but also plays an important role in colon tumor maintenance. In this study, we have investigated the role of p38 MAPK signaling in patient-derived xenografts (PDXs) from three different human colon tumors representing clinical heterogeneity and that recapitulate the human tumor conditions both at histological and molecular levels. We have found that PH797804, a chemical inhibitor of p38 MAPK, reduces tumor growth of the three PDXs, which correlates with impaired colon tumor cell proliferation and survival. The inhibition of p38 MAPK in PDXs results in downregulation of the IL-6/STAT3 signaling pathway, which is a key regulator of colon tumorigenesis. Our results show the importance of p38 MAPK in human colon tumor growth using a preclinical model, and support that inhibition of p38 MAPK signaling may have therapeutic interest for colon cancer treatment. Impact Journals LLC 2015-04-14 /pmc/articles/PMC4496165/ /pubmed/25890501 Text en Copyright: © 2015 Gupta et al. 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 Priority Research Paper
Gupta, Jalaj
Igea, Ana
Papaioannou, Marilena
Lopez-Casas, Pedro Pablo
Llonch, Elisabet
Hidalgo, Manuel
Gorgoulis, Vassilis G.
Nebreda, Angel R.
Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title_full Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title_fullStr Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title_full_unstemmed Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title_short Pharmacological inhibition of p38 MAPK reduces tumor growth in patient-derived xenografts from colon tumors
title_sort pharmacological inhibition of p38 mapk reduces tumor growth in patient-derived xenografts from colon tumors
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496165/
https://www.ncbi.nlm.nih.gov/pubmed/25890501
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