Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer

Abstract Triple-negative breast cancer (TNBC) is known for its aggressive nature, lack of effective diagnostic tools and treatments, and generally poor prognosis. The objective of this study was to investigate metabolic changes in TNBC using metabolomics approaches and explore the underlying mechani...

Full description

Saved in:
Bibliographic Details
Main Authors: Sisi Gong, Rongfu Huang, Meie Wang, Fen Lian, Qingshui Wang, Zhijun Liao, Chunmei Fan
Format: Article
Language:English
Published: BMC 2024-11-01
Series:Journal of Translational Medicine
Subjects:
Online Access:https://doi.org/10.1186/s12967-024-05843-y
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846164914863865856
author Sisi Gong
Rongfu Huang
Meie Wang
Fen Lian
Qingshui Wang
Zhijun Liao
Chunmei Fan
author_facet Sisi Gong
Rongfu Huang
Meie Wang
Fen Lian
Qingshui Wang
Zhijun Liao
Chunmei Fan
author_sort Sisi Gong
collection DOAJ
description Abstract Triple-negative breast cancer (TNBC) is known for its aggressive nature, lack of effective diagnostic tools and treatments, and generally poor prognosis. The objective of this study was to investigate metabolic changes in TNBC using metabolomics approaches and explore the underlying mechanisms through integrated analysis with transcriptomics. In this study, serum untargeted metabolic profiles were first examined between 18 TNBC patients and 21 healthy control (HC) subjects using liquid chromatography-mass spectrometry (LC-MS), identifying a total of 22 significantly differential metabolites (DMs). Subsequently, receiver operating characteristic analysis revealed that 7-methylguanine could serve as a potential biomarker for TNBC in both the discovery and validation sets. Additionally, transcriptomic datasets were retrieved from the GEO database to identify differentially expressed genes (DEGs) between TNBC and normal tissues. An integrative analysis of the DMs and DEGs was conducted, uncovering potential molecular mechanisms underlying TNBC. Notably, three pathways—tyrosine metabolism, phenylalanine metabolism, and glycolysis/gluconeogenesis—were enriched, providing insight into the energy metabolism disorders in TNBC. Within these pathways, two DMs (4-hydroxyphenylacetaldehyde and oxaloacetic acid) and six DEGs (MAOA, ADH1B, ADH1C, AOC3, TAT, and PCK1) were identified as key components. In summary, this study highlights metabolic biomarkers that could potentially be used for the diagnosis and screening of TNBC. The comprehensive analysis of metabolomics and transcriptomics data offers a validated and in-depth understanding of TNBC metabolism.
format Article
id doaj-art-97875ad73c8b4a82935e0960b0f2c609
institution Kabale University
issn 1479-5876
language English
publishDate 2024-11-01
publisher BMC
record_format Article
series Journal of Translational Medicine
spelling doaj-art-97875ad73c8b4a82935e0960b0f2c6092024-11-17T12:45:53ZengBMCJournal of Translational Medicine1479-58762024-11-0122111710.1186/s12967-024-05843-yComprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast CancerSisi Gong0Rongfu Huang1Meie Wang2Fen Lian3Qingshui Wang4Zhijun Liao5Chunmei Fan6The Clinical Laboratory Center, the Second Affiliated Hospital of Fujian Medical UniversityThe Clinical Laboratory Center, the Second Affiliated Hospital of Fujian Medical UniversityThe Clinical Laboratory Center, the Second Affiliated Hospital of Fujian Medical UniversityThe Clinical Laboratory Center, the Second Affiliated Hospital of Fujian Medical UniversityCollege of Integrative Medicine, Fujian University of Traditional Chinese MedicineDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fujian Medical UniversityThe Clinical Laboratory Center, the Second Affiliated Hospital of Fujian Medical UniversityAbstract Triple-negative breast cancer (TNBC) is known for its aggressive nature, lack of effective diagnostic tools and treatments, and generally poor prognosis. The objective of this study was to investigate metabolic changes in TNBC using metabolomics approaches and explore the underlying mechanisms through integrated analysis with transcriptomics. In this study, serum untargeted metabolic profiles were first examined between 18 TNBC patients and 21 healthy control (HC) subjects using liquid chromatography-mass spectrometry (LC-MS), identifying a total of 22 significantly differential metabolites (DMs). Subsequently, receiver operating characteristic analysis revealed that 7-methylguanine could serve as a potential biomarker for TNBC in both the discovery and validation sets. Additionally, transcriptomic datasets were retrieved from the GEO database to identify differentially expressed genes (DEGs) between TNBC and normal tissues. An integrative analysis of the DMs and DEGs was conducted, uncovering potential molecular mechanisms underlying TNBC. Notably, three pathways—tyrosine metabolism, phenylalanine metabolism, and glycolysis/gluconeogenesis—were enriched, providing insight into the energy metabolism disorders in TNBC. Within these pathways, two DMs (4-hydroxyphenylacetaldehyde and oxaloacetic acid) and six DEGs (MAOA, ADH1B, ADH1C, AOC3, TAT, and PCK1) were identified as key components. In summary, this study highlights metabolic biomarkers that could potentially be used for the diagnosis and screening of TNBC. The comprehensive analysis of metabolomics and transcriptomics data offers a validated and in-depth understanding of TNBC metabolism.https://doi.org/10.1186/s12967-024-05843-yTriple-negative breast cancerMetabolomicsTranscriptomicsBiomarkerPathways
spellingShingle Sisi Gong
Rongfu Huang
Meie Wang
Fen Lian
Qingshui Wang
Zhijun Liao
Chunmei Fan
Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
Journal of Translational Medicine
Triple-negative breast cancer
Metabolomics
Transcriptomics
Biomarker
Pathways
title Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
title_full Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
title_fullStr Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
title_full_unstemmed Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
title_short Comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of Triple Negative Breast Cancer
title_sort comprehensive analysis of the metabolomics and transcriptomics uncovers the dysregulated network and potential biomarkers of triple negative breast cancer
topic Triple-negative breast cancer
Metabolomics
Transcriptomics
Biomarker
Pathways
url https://doi.org/10.1186/s12967-024-05843-y
work_keys_str_mv AT sisigong comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT rongfuhuang comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT meiewang comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT fenlian comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT qingshuiwang comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT zhijunliao comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer
AT chunmeifan comprehensiveanalysisofthemetabolomicsandtranscriptomicsuncoversthedysregulatednetworkandpotentialbiomarkersoftriplenegativebreastcancer