Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice

Exposure to ionizing radiation disrupts metabolic pathways and causes oxidative stress, which can lead to organ damage. In this study, urinary metabolites from mice exposed to high-dose and low-dose whole-body irradiation (WBI HDR, WBI LDR) or partial-body irradiation (PBI BM2.5) were analyzed using...

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Main Authors: Yaoxiang Li, Shivani Bansal, Baldev Singh, Meth M. Jayatilake, William Klotzbier, Marjan Boerma, Mi-Heon Lee, Jacob Hack, Keisuke S. Iwamoto, Dörthe Schaue, Amrita K. Cheema
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Language:English
Published: MDPI AG 2024-12-01
Series:Antioxidants
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Online Access:https://www.mdpi.com/2076-3921/14/1/24
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author Yaoxiang Li
Shivani Bansal
Baldev Singh
Meth M. Jayatilake
William Klotzbier
Marjan Boerma
Mi-Heon Lee
Jacob Hack
Keisuke S. Iwamoto
Dörthe Schaue
Amrita K. Cheema
author_facet Yaoxiang Li
Shivani Bansal
Baldev Singh
Meth M. Jayatilake
William Klotzbier
Marjan Boerma
Mi-Heon Lee
Jacob Hack
Keisuke S. Iwamoto
Dörthe Schaue
Amrita K. Cheema
author_sort Yaoxiang Li
collection DOAJ
description Exposure to ionizing radiation disrupts metabolic pathways and causes oxidative stress, which can lead to organ damage. In this study, urinary metabolites from mice exposed to high-dose and low-dose whole-body irradiation (WBI HDR, WBI LDR) or partial-body irradiation (PBI BM2.5) were analyzed using targeted and untargeted metabolomics approaches. Significant metabolic changes particularly in oxidative stress pathways were observed on Day 2 post-radiation. By Day 30, the WBI HDR group showed persistent metabolic dysregulation, while the WBI LDR and PBI BM2.5 groups were similar to control mice. Machine learning models identified metabolites that were predictive of the type of radiation exposure with high accuracy, highlighting their potential use as biomarkers for radiation damage and oxidative stress.
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institution Kabale University
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publishDate 2024-12-01
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series Antioxidants
spelling doaj-art-78bd19c9170b47a8a01f706ad68517f72025-01-24T13:19:11ZengMDPI AGAntioxidants2076-39212024-12-011412410.3390/antiox14010024Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in MiceYaoxiang Li0Shivani Bansal1Baldev Singh2Meth M. Jayatilake3William Klotzbier4Marjan Boerma5Mi-Heon Lee6Jacob Hack7Keisuke S. Iwamoto8Dörthe Schaue9Amrita K. Cheema10Department of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Center, Washington, DC 20057, USADepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Center, Washington, DC 20057, USADepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Center, Washington, DC 20057, USADepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Center, Washington, DC 20057, USADepartments of Biochemistry, Molecular, and Cellular Biology, Georgetown University Medical Center, Washington, DC 20057, USADivision of Radiation Health, Department of Pharmaceutical Sciences, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USADepartment of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90024, USADepartment of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90024, USADepartment of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90024, USADepartment of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90024, USADepartment of Oncology, Lombardi Comprehensive Cancer Centre, Georgetown University Medical Center, Washington, DC 20057, USAExposure to ionizing radiation disrupts metabolic pathways and causes oxidative stress, which can lead to organ damage. In this study, urinary metabolites from mice exposed to high-dose and low-dose whole-body irradiation (WBI HDR, WBI LDR) or partial-body irradiation (PBI BM2.5) were analyzed using targeted and untargeted metabolomics approaches. Significant metabolic changes particularly in oxidative stress pathways were observed on Day 2 post-radiation. By Day 30, the WBI HDR group showed persistent metabolic dysregulation, while the WBI LDR and PBI BM2.5 groups were similar to control mice. Machine learning models identified metabolites that were predictive of the type of radiation exposure with high accuracy, highlighting their potential use as biomarkers for radiation damage and oxidative stress.https://www.mdpi.com/2076-3921/14/1/24radiation exposurewhole-body irradiationpartial-body irradiationmetabolomicsurine metabolomicspathway analysis
spellingShingle Yaoxiang Li
Shivani Bansal
Baldev Singh
Meth M. Jayatilake
William Klotzbier
Marjan Boerma
Mi-Heon Lee
Jacob Hack
Keisuke S. Iwamoto
Dörthe Schaue
Amrita K. Cheema
Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
Antioxidants
radiation exposure
whole-body irradiation
partial-body irradiation
metabolomics
urine metabolomics
pathway analysis
title Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
title_full Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
title_fullStr Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
title_full_unstemmed Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
title_short Distinct Urinary Metabolite Signatures Mirror In Vivo Oxidative Stress-Related Radiation Responses in Mice
title_sort distinct urinary metabolite signatures mirror in vivo oxidative stress related radiation responses in mice
topic radiation exposure
whole-body irradiation
partial-body irradiation
metabolomics
urine metabolomics
pathway analysis
url https://www.mdpi.com/2076-3921/14/1/24
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