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Increased formate overflow is a hallmark of oxidative cancer
Formate overflow coupled to mitochondrial oxidative metabolism\ has been observed in cancer cell lines, but whether that takes place in the tumor microenvironment is not known. Here we report the observation of serine catabolism to formate in normal murine tissues, with a relative rate correlating w...
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/PMC5893600/ https://www.ncbi.nlm.nih.gov/pubmed/29636461 http://dx.doi.org/10.1038/s41467-018-03777-w |
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author | Meiser, Johannes Schuster, Anne Pietzke, Matthias Vande Voorde, Johan Athineos, Dimitris Oizel, Kristell Burgos-Barragan, Guillermo Wit, Niek Dhayade, Sandeep Morton, Jennifer P. Dornier, Emmanuel Sumpton, David Mackay, Gillian M. Blyth, Karen Patel, Ketan J. Niclou, Simone P. Vazquez, Alexei |
author_facet | Meiser, Johannes Schuster, Anne Pietzke, Matthias Vande Voorde, Johan Athineos, Dimitris Oizel, Kristell Burgos-Barragan, Guillermo Wit, Niek Dhayade, Sandeep Morton, Jennifer P. Dornier, Emmanuel Sumpton, David Mackay, Gillian M. Blyth, Karen Patel, Ketan J. Niclou, Simone P. Vazquez, Alexei |
author_sort | Meiser, Johannes |
collection | PubMed |
description | Formate overflow coupled to mitochondrial oxidative metabolism\ has been observed in cancer cell lines, but whether that takes place in the tumor microenvironment is not known. Here we report the observation of serine catabolism to formate in normal murine tissues, with a relative rate correlating with serine levels and the tissue oxidative state. Yet, serine catabolism to formate is increased in the transformed tissue of in vivo models of intestinal adenomas and mammary carcinomas. The increased serine catabolism to formate is associated with increased serum formate levels. Finally, we show that inhibition of formate production by genetic interference reduces cancer cell invasion and this phenotype can be rescued by exogenous formate. We conclude that increased formate overflow is a hallmark of oxidative cancers and that high formate levels promote invasion via a yet unknown mechanism. |
format | Online Article Text |
id | pubmed-5893600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58936002018-04-13 Increased formate overflow is a hallmark of oxidative cancer Meiser, Johannes Schuster, Anne Pietzke, Matthias Vande Voorde, Johan Athineos, Dimitris Oizel, Kristell Burgos-Barragan, Guillermo Wit, Niek Dhayade, Sandeep Morton, Jennifer P. Dornier, Emmanuel Sumpton, David Mackay, Gillian M. Blyth, Karen Patel, Ketan J. Niclou, Simone P. Vazquez, Alexei Nat Commun Article Formate overflow coupled to mitochondrial oxidative metabolism\ has been observed in cancer cell lines, but whether that takes place in the tumor microenvironment is not known. Here we report the observation of serine catabolism to formate in normal murine tissues, with a relative rate correlating with serine levels and the tissue oxidative state. Yet, serine catabolism to formate is increased in the transformed tissue of in vivo models of intestinal adenomas and mammary carcinomas. The increased serine catabolism to formate is associated with increased serum formate levels. Finally, we show that inhibition of formate production by genetic interference reduces cancer cell invasion and this phenotype can be rescued by exogenous formate. We conclude that increased formate overflow is a hallmark of oxidative cancers and that high formate levels promote invasion via a yet unknown mechanism. Nature Publishing Group UK 2018-04-10 /pmc/articles/PMC5893600/ /pubmed/29636461 http://dx.doi.org/10.1038/s41467-018-03777-w 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 Meiser, Johannes Schuster, Anne Pietzke, Matthias Vande Voorde, Johan Athineos, Dimitris Oizel, Kristell Burgos-Barragan, Guillermo Wit, Niek Dhayade, Sandeep Morton, Jennifer P. Dornier, Emmanuel Sumpton, David Mackay, Gillian M. Blyth, Karen Patel, Ketan J. Niclou, Simone P. Vazquez, Alexei Increased formate overflow is a hallmark of oxidative cancer |
title | Increased formate overflow is a hallmark of oxidative cancer |
title_full | Increased formate overflow is a hallmark of oxidative cancer |
title_fullStr | Increased formate overflow is a hallmark of oxidative cancer |
title_full_unstemmed | Increased formate overflow is a hallmark of oxidative cancer |
title_short | Increased formate overflow is a hallmark of oxidative cancer |
title_sort | increased formate overflow is a hallmark of oxidative cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893600/ https://www.ncbi.nlm.nih.gov/pubmed/29636461 http://dx.doi.org/10.1038/s41467-018-03777-w |
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