Lipidomic study of cell lines reveals lipid biomarkers for breast cancer subtypes

This work was supported by the Icelandic Centre for Research, Reykjavik, Iceland (project grant no. 174566051) and the University of Iceland Research Fund, Reykjavik, Iceland. The funding supplied the salary for MKN. The funders had no role in study design, data collection and analysis, decision to...

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Bibliographic Details
Published in:PLOS ONE
Main Authors: Eiríksson, Finnur Freyr, Nøhr, Martha Kampp, Costa, Margarida, Bodvarsdottir, Sigridur Klara, Ögmundsdóttir, Helga M, Þorsteinsdóttir, Margrét
Other Authors: Faculty of Medicine, Faculty of Pharmaceutical Sciences, Health Sciences
Format: Article in Journal/Newspaper
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/20.500.11815/4034
https://doi.org/10.1371/journal.pone.0231289
Description
Summary:This work was supported by the Icelandic Centre for Research, Reykjavik, Iceland (project grant no. 174566051) and the University of Iceland Research Fund, Reykjavik, Iceland. The funding supplied the salary for MKN. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Breast cancer (BC) is the most prevalent type of cancer in women in western countries. BC mortality has not declined despite early detection by screening, indicating the need for better informed treatment decisions. Therefore, a novel noninvasive diagnostic tool for BC would give the opportunity of subtype-specific treatment and improved prospects for the patients. Heterogeneity of BC tumor subtypes is reflected in the expression levels of enzymes in lipid metabolism. The aim of the study was to investigate whether the subtype defined by the transcriptome is reflected in the lipidome of BC cell lines. A liquid chromatography mass spectrometry (LC-MS) platform was applied to analyze the lipidome of six cell lines derived from human BC cell lines representing different BC subtypes. We identified an increased abundance of triacylglycerols (TG) ≥ C-48 with moderate or multiple unsaturation in fatty acyl chains and down-regulated ether-phosphatidylethanolamines (PE) (C-34 to C-38) in cell lines representing estrogen receptor and progesterone receptor positive tumor subtypes. In a cell line representing HER2-overexpressing tumor subtype an elevated expression of TG (≤ C-46), phosphatidylcholines (PC) and PE containing short-chained (≤ C-16) saturated or monounsaturated fatty acids were observed. Increased abundance of PC ≥ C-40 was found in cell lines of triple negative BC subtype. In addition, differences were detected in lipidomes within these previously defined subtypes. We conclude that subtypes defined by the transcriptome are indeed reflected in differences in the lipidome and, furthermore, potentially biologically relevant differences may exist within these defined ...