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Biosynthetic energy cost for amino acids decreases in cancer evolution

Rapidly proliferating cancer cells have much higher demand for proteinogenic amino acids than normal cells. The use of amino acids in human proteomes is largely affected by their bioavailability, which is constrained by the biosynthetic energy cost in living organisms. Conceptually distinct from gen...

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Detalles Bibliográficos
Autores principales: Zhang, Hong, Wang, Yirong, Li, Jun, Chen, Han, He, Xionglei, Zhang, Huiwen, Liang, Han, Lu, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175916/
https://www.ncbi.nlm.nih.gov/pubmed/30297703
http://dx.doi.org/10.1038/s41467-018-06461-1
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author Zhang, Hong
Wang, Yirong
Li, Jun
Chen, Han
He, Xionglei
Zhang, Huiwen
Liang, Han
Lu, Jian
author_facet Zhang, Hong
Wang, Yirong
Li, Jun
Chen, Han
He, Xionglei
Zhang, Huiwen
Liang, Han
Lu, Jian
author_sort Zhang, Hong
collection PubMed
description Rapidly proliferating cancer cells have much higher demand for proteinogenic amino acids than normal cells. The use of amino acids in human proteomes is largely affected by their bioavailability, which is constrained by the biosynthetic energy cost in living organisms. Conceptually distinct from gene-based analyses, we introduce the energy cost per amino acid (ECPA) to quantitatively characterize the use of 20 amino acids during protein synthesis in human cells. By analyzing gene expression data from The Cancer Genome Atlas, we find that cancer cells evolve to utilize amino acids more economically by optimizing gene expression profile and ECPA shows robust prognostic power across many cancer types. We further validate this pattern in an experimental evolution of xenograft tumors. Our ECPA analysis reveals a common principle during cancer evolution.
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spelling pubmed-61759162018-10-11 Biosynthetic energy cost for amino acids decreases in cancer evolution Zhang, Hong Wang, Yirong Li, Jun Chen, Han He, Xionglei Zhang, Huiwen Liang, Han Lu, Jian Nat Commun Article Rapidly proliferating cancer cells have much higher demand for proteinogenic amino acids than normal cells. The use of amino acids in human proteomes is largely affected by their bioavailability, which is constrained by the biosynthetic energy cost in living organisms. Conceptually distinct from gene-based analyses, we introduce the energy cost per amino acid (ECPA) to quantitatively characterize the use of 20 amino acids during protein synthesis in human cells. By analyzing gene expression data from The Cancer Genome Atlas, we find that cancer cells evolve to utilize amino acids more economically by optimizing gene expression profile and ECPA shows robust prognostic power across many cancer types. We further validate this pattern in an experimental evolution of xenograft tumors. Our ECPA analysis reveals a common principle during cancer evolution. Nature Publishing Group UK 2018-10-08 /pmc/articles/PMC6175916/ /pubmed/30297703 http://dx.doi.org/10.1038/s41467-018-06461-1 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
Zhang, Hong
Wang, Yirong
Li, Jun
Chen, Han
He, Xionglei
Zhang, Huiwen
Liang, Han
Lu, Jian
Biosynthetic energy cost for amino acids decreases in cancer evolution
title Biosynthetic energy cost for amino acids decreases in cancer evolution
title_full Biosynthetic energy cost for amino acids decreases in cancer evolution
title_fullStr Biosynthetic energy cost for amino acids decreases in cancer evolution
title_full_unstemmed Biosynthetic energy cost for amino acids decreases in cancer evolution
title_short Biosynthetic energy cost for amino acids decreases in cancer evolution
title_sort biosynthetic energy cost for amino acids decreases in cancer evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175916/
https://www.ncbi.nlm.nih.gov/pubmed/30297703
http://dx.doi.org/10.1038/s41467-018-06461-1
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