Metabolomics in hepatocellular carcinoma: From biomarker discovery to precision medicine
Hepatocellular carcinoma (HCC) remains a global health burden, and is mostly diagnosed at late and advanced stages. Currently, limited and insensitive diagnostic modalities continue to be the bottleneck of effective and tailored therapy for HCC patients. Moreover, the complex reprogramming of metabo...
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Published in | Frontiers in medical technology Vol. 4; p. 1065506 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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04.01.2023
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ISSN | 2673-3129 2673-3129 |
DOI | 10.3389/fmedt.2022.1065506 |
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Abstract | Hepatocellular carcinoma (HCC) remains a global health burden, and is mostly diagnosed at late and advanced stages. Currently, limited and insensitive diagnostic modalities continue to be the bottleneck of effective and tailored therapy for HCC patients. Moreover, the complex reprogramming of metabolic patterns during HCC initiation and progression has been obstructing the precision medicine in clinical practice. As a noninvasive and global screening approach, metabolomics serves as a powerful tool to dynamically monitor metabolic patterns and identify promising metabolite biomarkers, therefore holds a great potential for the development of tailored therapy for HCC patients. In this review, we summarize the recent advances in HCC metabolomics studies, including metabolic alterations associated with HCC progression, as well as novel metabolite biomarkers for HCC diagnosis, monitor, and prognostic evaluation. Moreover, we highlight the application of multi-omics strategies containing metabolomics in biomarker discovery for HCC. Notably, we also discuss the opportunities and challenges of metabolomics in nowadays HCC precision medicine. As technologies improving and metabolite biomarkers discovering, metabolomics has made a major step toward more timely and effective precision medicine for HCC patients. |
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AbstractList | Hepatocellular carcinoma (HCC) remains a global health burden, and is mostly diagnosed at late and advanced stages. Currently, limited and insensitive diagnostic modalities continue to be the bottleneck of effective and tailored therapy for HCC patients. Moreover, the complex reprogramming of metabolic patterns during HCC initiation and progression has been obstructing the precision medicine in clinical practice. As a noninvasive and global screening approach, metabolomics serves as a powerful tool to dynamically monitor metabolic patterns and identify promising metabolite biomarkers, therefore holds a great potential for the development of tailored therapy for HCC patients. In this review, we summarize the recent advances in HCC metabolomics studies, including metabolic alterations associated with HCC progression, as well as novel metabolite biomarkers for HCC diagnosis, monitor, and prognostic evaluation. Moreover, we highlight the application of multi-omics strategies containing metabolomics in biomarker discovery for HCC. Notably, we also discuss the opportunities and challenges of metabolomics in nowadays HCC precision medicine. As technologies improving and metabolite biomarkers discovering, metabolomics has made a major step toward more timely and effective precision medicine for HCC patients. Hepatocellular carcinoma (HCC) remains a global health burden, and is mostly diagnosed at late and advanced stages. Currently, limited and insensitive diagnostic modalities continue to be the bottleneck of effective and tailored therapy for HCC patients. Moreover, the complex reprogramming of metabolic patterns during HCC initiation and progression has been obstructing the precision medicine in clinical practice. As a noninvasive and global screening approach, metabolomics serves as a powerful tool to dynamically monitor metabolic patterns and identify promising metabolite biomarkers, therefore holds a great potential for the development of tailored therapy for HCC patients. In this review, we summarize the recent advances in HCC metabolomics studies, including metabolic alterations associated with HCC progression, as well as novel metabolite biomarkers for HCC diagnosis, monitor, and prognostic evaluation. Moreover, we highlight the application of multi-omics strategies containing metabolomics in biomarker discovery for HCC. Notably, we also discuss the opportunities and challenges of metabolomics in nowadays HCC precision medicine. As technologies improving and metabolite biomarkers discovering, metabolomics has made a major step toward more timely and effective precision medicine for HCC patients.Hepatocellular carcinoma (HCC) remains a global health burden, and is mostly diagnosed at late and advanced stages. Currently, limited and insensitive diagnostic modalities continue to be the bottleneck of effective and tailored therapy for HCC patients. Moreover, the complex reprogramming of metabolic patterns during HCC initiation and progression has been obstructing the precision medicine in clinical practice. As a noninvasive and global screening approach, metabolomics serves as a powerful tool to dynamically monitor metabolic patterns and identify promising metabolite biomarkers, therefore holds a great potential for the development of tailored therapy for HCC patients. In this review, we summarize the recent advances in HCC metabolomics studies, including metabolic alterations associated with HCC progression, as well as novel metabolite biomarkers for HCC diagnosis, monitor, and prognostic evaluation. Moreover, we highlight the application of multi-omics strategies containing metabolomics in biomarker discovery for HCC. Notably, we also discuss the opportunities and challenges of metabolomics in nowadays HCC precision medicine. As technologies improving and metabolite biomarkers discovering, metabolomics has made a major step toward more timely and effective precision medicine for HCC patients. |
Author | Wang, Zihao Wang, Kui Shu, Dan Wu, Xingyun Luo, Li |
AuthorAffiliation | 4 Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University) , Ministry of Education , Chengdu , China 5 School of Bioscience and Technology , Chengdu Medical College , Chengdu , China 3 Center for Reproductive Medicine, Department of Gynecology and Obstetrics , West China Second University Hospital, Sichuan University , Chengdu , China 1 West China School of Basic Medical Science & Forensic Medicine , Sichuan University , Chengdu , China 2 Department of Gastrointestinal Surgery , West China Hospital, Sichuan University , Chengdu , China |
AuthorAffiliation_xml | – name: 5 School of Bioscience and Technology , Chengdu Medical College , Chengdu , China – name: 1 West China School of Basic Medical Science & Forensic Medicine , Sichuan University , Chengdu , China – name: 3 Center for Reproductive Medicine, Department of Gynecology and Obstetrics , West China Second University Hospital, Sichuan University , Chengdu , China – name: 4 Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University) , Ministry of Education , Chengdu , China – name: 2 Department of Gastrointestinal Surgery , West China Hospital, Sichuan University , Chengdu , China |
Author_xml | – sequence: 1 givenname: Xingyun surname: Wu fullname: Wu, Xingyun – sequence: 2 givenname: Zihao surname: Wang fullname: Wang, Zihao – sequence: 3 givenname: Li surname: Luo fullname: Luo, Li – sequence: 4 givenname: Dan surname: Shu fullname: Shu, Dan – sequence: 5 givenname: Kui surname: Wang fullname: Wang, Kui |
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Keywords | multi-omics precision medicine metabolomics biomarkers hepatocellular carcinoma |
Language | English |
License | 2023 Wu, Wang, Luo, Shu and Wang. 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. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Abbreviations HCC, hepatocellular carcinoma; HBV, hepatitis B virus; HCV, hepatitis C virus; NAFLD, non-alcoholic fatty liver disease; AFP, α-fetoprotein; NMR, nuclear magnetic resonance; MS, mass spectrometry; DEN, diethyl-nitrosamine; GC, gas chromatography; LC, liquid chromatography; CE, capillary electrophoresis; FFA, free fatty acid; ESI, electrospray ionization; FT-ICR, Fourier transform ion cyclotron resonance; TOF, time of flight; Q, quadrupole; SRM, selected reaction monitoring; MRM, multiple reaction monitoring; PCA, principal component analysis; PLS-DA, partial least squares regression discriminant analysis; OPLS, orthogonal partial last squares; ROC, receiver operating characteristic; NFSM, network-based feature selection method; UPLC, ultra-performance liquid chromatographic; LASSO, least absolute shrinkage and selection operator; TACE, transcatheter arterial chemoembolization; RFA, radiofrequency ablation; UGPase 2, uridine diphosphate glucose pyrophosphorylase 2; TP53, tumor protein p53; TCF1, transcription factor 1; SCD, stearoyl-CoA-desaturase; HBc, hepatitis B virus core protein; GO, Gene Ontology; KEGG, Kyoto Encyclopedia of Genes and Genomes pathway. Edited by: Chon Lok Lei, University of Macau, China Specialty Section: This article was submitted to Medtech Data Analytics, a section of the journal Frontiers in Medical Technology These authors have contributed equally to this work and share first authorship Reviewed by: Xuefeng Li, University of Texas MD Anderson Cancer Center, United States Xiaonan Zheng, University of Oxford, United Kingdom |
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