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Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis

Metabolic rewiring is a critical hallmark of tumorigenesis and is essential for the development of cancer. Although many key features of metabolic alteration that are crucial for tumor cell survival, proliferation and progression have been identified, these are obtained from studies with established...

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Autores principales: Myllymäki, Henna, Astorga Johansson, Jeanette, Grados Porro, Estefania, Elliot, Abigail, Moses, Tessa, Feng, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369915/
https://www.ncbi.nlm.nih.gov/pubmed/34414180
http://dx.doi.org/10.3389/fcell.2021.684036
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author Myllymäki, Henna
Astorga Johansson, Jeanette
Grados Porro, Estefania
Elliot, Abigail
Moses, Tessa
Feng, Yi
author_facet Myllymäki, Henna
Astorga Johansson, Jeanette
Grados Porro, Estefania
Elliot, Abigail
Moses, Tessa
Feng, Yi
author_sort Myllymäki, Henna
collection PubMed
description Metabolic rewiring is a critical hallmark of tumorigenesis and is essential for the development of cancer. Although many key features of metabolic alteration that are crucial for tumor cell survival, proliferation and progression have been identified, these are obtained from studies with established tumors and cancer cell lines. However, information on the essential metabolic changes that occur during pre-neoplastic cell (PNC) development that enables its progression to full blown tumor is still lacking. Here, we present an untargeted metabolomics analysis of human oncogene HRAS(G12V) induced PNC development, using a transgenic inducible zebrafish larval skin development model. By comparison with normal sibling controls, we identified six metabolic pathways that are significantly altered during PNC development in the skin. Amongst these altered pathways are pyrimidine, purine and amino acid metabolism that are common to the cancer metabolic changes that support rapid cell proliferation and growth. Our data also suggest alterations in post transcriptional modification of RNAs that might play a role in PNC development. Our study provides a proof of principle work flow for identifying metabolic alterations during PNC development driven by an oncogenic mutation. In the future, this approach could be combined with transcriptomic or proteomic approaches to establish the detailed interaction between signaling networks and cellular metabolic pathways that occur at the onset of tumor progression.
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spelling pubmed-83699152021-08-18 Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis Myllymäki, Henna Astorga Johansson, Jeanette Grados Porro, Estefania Elliot, Abigail Moses, Tessa Feng, Yi Front Cell Dev Biol Cell and Developmental Biology Metabolic rewiring is a critical hallmark of tumorigenesis and is essential for the development of cancer. Although many key features of metabolic alteration that are crucial for tumor cell survival, proliferation and progression have been identified, these are obtained from studies with established tumors and cancer cell lines. However, information on the essential metabolic changes that occur during pre-neoplastic cell (PNC) development that enables its progression to full blown tumor is still lacking. Here, we present an untargeted metabolomics analysis of human oncogene HRAS(G12V) induced PNC development, using a transgenic inducible zebrafish larval skin development model. By comparison with normal sibling controls, we identified six metabolic pathways that are significantly altered during PNC development in the skin. Amongst these altered pathways are pyrimidine, purine and amino acid metabolism that are common to the cancer metabolic changes that support rapid cell proliferation and growth. Our data also suggest alterations in post transcriptional modification of RNAs that might play a role in PNC development. Our study provides a proof of principle work flow for identifying metabolic alterations during PNC development driven by an oncogenic mutation. In the future, this approach could be combined with transcriptomic or proteomic approaches to establish the detailed interaction between signaling networks and cellular metabolic pathways that occur at the onset of tumor progression. Frontiers Media S.A. 2021-08-03 /pmc/articles/PMC8369915/ /pubmed/34414180 http://dx.doi.org/10.3389/fcell.2021.684036 Text en Copyright © 2021 Myllymäki, Astorga Johansson, Grados Porro, Elliot, Moses and Feng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Myllymäki, Henna
Astorga Johansson, Jeanette
Grados Porro, Estefania
Elliot, Abigail
Moses, Tessa
Feng, Yi
Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title_full Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title_fullStr Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title_full_unstemmed Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title_short Metabolic Alterations in Preneoplastic Development Revealed by Untargeted Metabolomic Analysis
title_sort metabolic alterations in preneoplastic development revealed by untargeted metabolomic analysis
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8369915/
https://www.ncbi.nlm.nih.gov/pubmed/34414180
http://dx.doi.org/10.3389/fcell.2021.684036
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