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Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study

BACKGROUND: The serum metabolome is a potential source of molecular biomarkers associated with the risk of breast cancer. Here we aimed to analyze metabolites present in pre-diagnostic serum samples collected from healthy women participating in the Norwegian Trøndelag Health Study (HUNT2 study) for...

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Autores principales: Mrowiec, Katarzyna, Kurczyk, Agata, Jelonek, Karol, Debik, Julia, Giskeødegård, Guro F., Bathen, Tone F., Widłak, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061137/
https://www.ncbi.nlm.nih.gov/pubmed/37007110
http://dx.doi.org/10.3389/fonc.2023.1116806
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author Mrowiec, Katarzyna
Kurczyk, Agata
Jelonek, Karol
Debik, Julia
Giskeødegård, Guro F.
Bathen, Tone F.
Widłak, Piotr
author_facet Mrowiec, Katarzyna
Kurczyk, Agata
Jelonek, Karol
Debik, Julia
Giskeødegård, Guro F.
Bathen, Tone F.
Widłak, Piotr
author_sort Mrowiec, Katarzyna
collection PubMed
description BACKGROUND: The serum metabolome is a potential source of molecular biomarkers associated with the risk of breast cancer. Here we aimed to analyze metabolites present in pre-diagnostic serum samples collected from healthy women participating in the Norwegian Trøndelag Health Study (HUNT2 study) for whom long-term information about developing breast cancer was available. METHODS: Women participating in the HUNT2 study who developed breast cancer within a 15-year follow-up period (BC cases) and age-matched women who stayed breast cancer-free were selected (n=453 case-control pairs). Using a high-resolution mass spectrometry approach 284 compounds were quantitatively analyzed, including 30 amino acids and biogenic amines, hexoses, and 253 lipids (acylcarnitines, glycerides, phosphatidylcholines, sphingolipids, and cholesteryl esters). RESULTS: Age was a major confounding factor responsible for a large heterogeneity in the dataset, hence age-defined subgroups were analyzed separately. The largest number of metabolites whose serum levels differentiated BC cases and controls (82 compounds) were observed in the subgroup of younger women (<45 years old). Noteworthy, increased levels of glycerides, phosphatidylcholines, and sphingolipids were associated with reduced risk of cancer in younger and middle-aged women (≤64 years old). On the other hand, increased levels of serum lipids were associated with an enhanced risk of breast cancer in older women (>64 years old). Moreover, several metabolites could be detected whose serum levels were different between BC cases diagnosed earlier (<5 years) and later (>10 years) after sample collecting, yet these compounds were also correlated with the age of participants. Current results were coherent with the results of the NMR-based metabolomics study performed in the cohort of HUNT2 participants, where increased serum levels of VLDL subfractions were associated with reduced risk of breast cancer in premenopausal women. CONCLUSIONS: Changes in metabolite levels detected in pre-diagnostic serum samples, which reflected an impaired lipid and amino acid metabolism, were associated with long-term risk of breast cancer in an age-dependent manner.
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spelling pubmed-100611372023-03-31 Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study Mrowiec, Katarzyna Kurczyk, Agata Jelonek, Karol Debik, Julia Giskeødegård, Guro F. Bathen, Tone F. Widłak, Piotr Front Oncol Oncology BACKGROUND: The serum metabolome is a potential source of molecular biomarkers associated with the risk of breast cancer. Here we aimed to analyze metabolites present in pre-diagnostic serum samples collected from healthy women participating in the Norwegian Trøndelag Health Study (HUNT2 study) for whom long-term information about developing breast cancer was available. METHODS: Women participating in the HUNT2 study who developed breast cancer within a 15-year follow-up period (BC cases) and age-matched women who stayed breast cancer-free were selected (n=453 case-control pairs). Using a high-resolution mass spectrometry approach 284 compounds were quantitatively analyzed, including 30 amino acids and biogenic amines, hexoses, and 253 lipids (acylcarnitines, glycerides, phosphatidylcholines, sphingolipids, and cholesteryl esters). RESULTS: Age was a major confounding factor responsible for a large heterogeneity in the dataset, hence age-defined subgroups were analyzed separately. The largest number of metabolites whose serum levels differentiated BC cases and controls (82 compounds) were observed in the subgroup of younger women (<45 years old). Noteworthy, increased levels of glycerides, phosphatidylcholines, and sphingolipids were associated with reduced risk of cancer in younger and middle-aged women (≤64 years old). On the other hand, increased levels of serum lipids were associated with an enhanced risk of breast cancer in older women (>64 years old). Moreover, several metabolites could be detected whose serum levels were different between BC cases diagnosed earlier (<5 years) and later (>10 years) after sample collecting, yet these compounds were also correlated with the age of participants. Current results were coherent with the results of the NMR-based metabolomics study performed in the cohort of HUNT2 participants, where increased serum levels of VLDL subfractions were associated with reduced risk of breast cancer in premenopausal women. CONCLUSIONS: Changes in metabolite levels detected in pre-diagnostic serum samples, which reflected an impaired lipid and amino acid metabolism, were associated with long-term risk of breast cancer in an age-dependent manner. Frontiers Media S.A. 2023-03-16 /pmc/articles/PMC10061137/ /pubmed/37007110 http://dx.doi.org/10.3389/fonc.2023.1116806 Text en Copyright © 2023 Mrowiec, Kurczyk, Jelonek, Debik, Giskeødegård, Bathen and Widłak 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 Oncology
Mrowiec, Katarzyna
Kurczyk, Agata
Jelonek, Karol
Debik, Julia
Giskeødegård, Guro F.
Bathen, Tone F.
Widłak, Piotr
Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title_full Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title_fullStr Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title_full_unstemmed Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title_short Association of serum metabolome profile with the risk of breast cancer in participants of the HUNT2 study
title_sort association of serum metabolome profile with the risk of breast cancer in participants of the hunt2 study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10061137/
https://www.ncbi.nlm.nih.gov/pubmed/37007110
http://dx.doi.org/10.3389/fonc.2023.1116806
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