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Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia

BACKGROUND: Cancer cells modify the balance between fatty acid (FA) synthesis and uptake under metabolic stress, induced by oxygen/nutrient deprivation. These modifications were shown to alter the levels of individual triglyceride (TG) or phospholipid sub-species. To attain a holistic overview of th...

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Autores principales: Lisec, Jan, Jaeger, Carsten, Rashid, Rida, Munir, Rimsha, Zaidi, Nousheen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537432/
https://www.ncbi.nlm.nih.gov/pubmed/31138183
http://dx.doi.org/10.1186/s12885-019-5733-y
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author Lisec, Jan
Jaeger, Carsten
Rashid, Rida
Munir, Rimsha
Zaidi, Nousheen
author_facet Lisec, Jan
Jaeger, Carsten
Rashid, Rida
Munir, Rimsha
Zaidi, Nousheen
author_sort Lisec, Jan
collection PubMed
description BACKGROUND: Cancer cells modify the balance between fatty acid (FA) synthesis and uptake under metabolic stress, induced by oxygen/nutrient deprivation. These modifications were shown to alter the levels of individual triglyceride (TG) or phospholipid sub-species. To attain a holistic overview of the lipidomic profiles of cancer cells under stress we performed a broad lipidomic assay, comprising 244 lipids from six major classes. This assay allowed us to perform robust analyses and assess the changes in averages of broader lipid-classes, stratified on the basis of saturation index of their fatty-acyl side chains. METHODS: Global lipidomic profiling using Liquid Chromatography-Mass Spectrometry was performed to assess lipidomic profiles of biologically diverse cancer cell lines cultivated under metabolically stressed conditions. RESULTS: Neutral lipid compositions were markedly modified under serum-deprived conditions and, strikingly, the cellular level of triglyceride subspecies decreased with increasing number of double bonds in their fatty acyl chains. In contrast and unexpectedly, no robust changes were observed in lipidomic profiles of hypoxic (2% O(2)) cancer cells despite concurrent changes in proliferation rates and metabolic gene expression. CONCLUSIONS: Serum-deprivation significantly affects lipidomic profiles of cancer cells. Although, the levels of individual lipid moieties alter under hypoxia (2% O(2)), the robust averages of broader lipid classes remain unchanged. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5733-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-65374322019-05-30 Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia Lisec, Jan Jaeger, Carsten Rashid, Rida Munir, Rimsha Zaidi, Nousheen BMC Cancer Research Article BACKGROUND: Cancer cells modify the balance between fatty acid (FA) synthesis and uptake under metabolic stress, induced by oxygen/nutrient deprivation. These modifications were shown to alter the levels of individual triglyceride (TG) or phospholipid sub-species. To attain a holistic overview of the lipidomic profiles of cancer cells under stress we performed a broad lipidomic assay, comprising 244 lipids from six major classes. This assay allowed us to perform robust analyses and assess the changes in averages of broader lipid-classes, stratified on the basis of saturation index of their fatty-acyl side chains. METHODS: Global lipidomic profiling using Liquid Chromatography-Mass Spectrometry was performed to assess lipidomic profiles of biologically diverse cancer cell lines cultivated under metabolically stressed conditions. RESULTS: Neutral lipid compositions were markedly modified under serum-deprived conditions and, strikingly, the cellular level of triglyceride subspecies decreased with increasing number of double bonds in their fatty acyl chains. In contrast and unexpectedly, no robust changes were observed in lipidomic profiles of hypoxic (2% O(2)) cancer cells despite concurrent changes in proliferation rates and metabolic gene expression. CONCLUSIONS: Serum-deprivation significantly affects lipidomic profiles of cancer cells. Although, the levels of individual lipid moieties alter under hypoxia (2% O(2)), the robust averages of broader lipid classes remain unchanged. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-019-5733-y) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-28 /pmc/articles/PMC6537432/ /pubmed/31138183 http://dx.doi.org/10.1186/s12885-019-5733-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Lisec, Jan
Jaeger, Carsten
Rashid, Rida
Munir, Rimsha
Zaidi, Nousheen
Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title_full Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title_fullStr Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title_full_unstemmed Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title_short Cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
title_sort cancer cell lipid class homeostasis is altered under nutrient-deprivation but stable under hypoxia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537432/
https://www.ncbi.nlm.nih.gov/pubmed/31138183
http://dx.doi.org/10.1186/s12885-019-5733-y
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