A plasma metabolite panel as biomarkers for early primary breast cancer detection.


Journal

International journal of cancer
ISSN: 1097-0215
Titre abrégé: Int J Cancer
Pays: United States
ID NLM: 0042124

Informations de publication

Date de publication:
01 06 2019
Historique:
received: 26 06 2018
revised: 19 09 2018
accepted: 16 10 2018
pubmed: 15 11 2018
medline: 4 9 2019
entrez: 15 11 2018
Statut: ppublish

Résumé

In recent years, metabolites have attracted substantial attention as promising novel biomarkers of various diseases. However, breast cancer plasma metabolite studies are still in their infancy. Here, we investigated the potential of metabolites to serve as minimally invasive, early detection markers of primary breast cancer. We profiled metabolites extracted from the plasma of primary breast cancer patients and healthy controls using tandem mass spectrometry (UHPLC-MS/MS and FIA-MS/MS). Two metabolites were found to be upregulated, while 16 metabolites were downregulated in primary breast cancer patients compared to healthy controls in both the training and validation cohorts. A panel of seven metabolites was selected by LASSO regression analysis. This panel could differentiate primary breast cancer patients from healthy controls, with an AUC of 0.87 (95% CI: 0.81 ~ 0.92) in the training cohort and an AUC of 0.80 (95% CI: 0.71 ~ 0.87) in the validation cohort. These significantly differentiated metabolites are mainly involved in the amino acid metabolism and breast cancer cell growth pathways. In conclusion, using a metabolomics approach, we identified metabolites that have potential value for development of a multimarker blood-based test to complement and improve early breast cancer detection. The panel identified herein might be part of a prescreening tool, especially for younger women or for closely observing women with certain risks, to facilitate decision making regarding which individuals should undergo further diagnostic tests. In the future, the combination of metabolites and other blood-based molecular marker sets, such as DNA methylation, microRNA, and cell-free DNA mutation markers, will be an attractive option.

Identifiants

pubmed: 30426507
doi: 10.1002/ijc.31996
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2833-2842

Informations de copyright

© 2018 UICC.

Auteurs

Baowen Yuan (B)

Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.
Division of Molecular Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Simon Schafferer (S)

Biocrates Life Sciences AG, Innsbruck, Austria.

Qiuqiong Tang (Q)

Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.
Division of Molecular Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Matthias Scheffler (M)

Biocrates Life Sciences AG, Innsbruck, Austria.

Juliane Nees (J)

National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Jörg Heil (J)

Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Sarah Schott (S)

Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Michael Golatta (M)

Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Markus Wallwiener (M)

National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Christof Sohn (C)

Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Therese Koal (T)

Biocrates Life Sciences AG, Innsbruck, Austria.

Barbara Wolf (B)

Biocrates Life Sciences AG, Innsbruck, Austria.

Andreas Schneeweiß (A)

National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.

Barbara Burwinkel (B)

Molecular Biology of Breast Cancer, Department of Gynecology and Obstetrics, University of Heidelberg, Heidelberg, Germany.
Division of Molecular Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

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