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Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner
Liver is an important secretory organ that consistently manages various insults in order to retain whole-body homeostasis. Importantly, it was suggested that the tumor-suppressor p53 plays a role in a variety of liver physiological processes and thus it is being regarded as a systemic homeostasis re...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974134/ https://www.ncbi.nlm.nih.gov/pubmed/29844359 http://dx.doi.org/10.1038/s41419-018-0697-4 |
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author | Charni-Natan, Meital Solomon, Hilla Molchadsky, Alina Jacob-Berger, Adi Goldfinger, Naomi Rotter, Varda |
author_facet | Charni-Natan, Meital Solomon, Hilla Molchadsky, Alina Jacob-Berger, Adi Goldfinger, Naomi Rotter, Varda |
author_sort | Charni-Natan, Meital |
collection | PubMed |
description | Liver is an important secretory organ that consistently manages various insults in order to retain whole-body homeostasis. Importantly, it was suggested that the tumor-suppressor p53 plays a role in a variety of liver physiological processes and thus it is being regarded as a systemic homeostasis regulator. Using high-throughput mass spectrometric analysis, we identified various p53-dependent liver secretome profiles. This allowed a global view on the role of p53 in maintaining the harmony of liver and whole-body homeostasis. We found that p53 altered the liver secretome differently under various conditions. Under physiological conditions, p53 controls factors that are related mainly to lipid metabolism and injury response. Upon exposure to various types of cancer therapy agents, the hepatic p53 is activated and induces the secretion of proteins related to additional pathways, such as hemostasis, immune response, and cell adhesion. Interestingly, we identified a possible relationship between p53-dependent liver functions and lung tumors. The latter modify differently liver secretome profile toward the secretion of proteins mainly related to cell migration and immune response. The notion that p53 may rewire the liver secretome profile suggests a new non-cell autonomous role of p53 that affect different liver functions and whole organism homeostasis. |
format | Online Article Text |
id | pubmed-5974134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59741342018-05-30 Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner Charni-Natan, Meital Solomon, Hilla Molchadsky, Alina Jacob-Berger, Adi Goldfinger, Naomi Rotter, Varda Cell Death Dis Article Liver is an important secretory organ that consistently manages various insults in order to retain whole-body homeostasis. Importantly, it was suggested that the tumor-suppressor p53 plays a role in a variety of liver physiological processes and thus it is being regarded as a systemic homeostasis regulator. Using high-throughput mass spectrometric analysis, we identified various p53-dependent liver secretome profiles. This allowed a global view on the role of p53 in maintaining the harmony of liver and whole-body homeostasis. We found that p53 altered the liver secretome differently under various conditions. Under physiological conditions, p53 controls factors that are related mainly to lipid metabolism and injury response. Upon exposure to various types of cancer therapy agents, the hepatic p53 is activated and induces the secretion of proteins related to additional pathways, such as hemostasis, immune response, and cell adhesion. Interestingly, we identified a possible relationship between p53-dependent liver functions and lung tumors. The latter modify differently liver secretome profile toward the secretion of proteins mainly related to cell migration and immune response. The notion that p53 may rewire the liver secretome profile suggests a new non-cell autonomous role of p53 that affect different liver functions and whole organism homeostasis. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974134/ /pubmed/29844359 http://dx.doi.org/10.1038/s41419-018-0697-4 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Charni-Natan, Meital Solomon, Hilla Molchadsky, Alina Jacob-Berger, Adi Goldfinger, Naomi Rotter, Varda Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title | Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title_full | Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title_fullStr | Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title_full_unstemmed | Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title_short | Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
title_sort | various stress stimuli rewire the profile of liver secretome in a p53-dependent manner |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974134/ https://www.ncbi.nlm.nih.gov/pubmed/29844359 http://dx.doi.org/10.1038/s41419-018-0697-4 |
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