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Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma

BACKGROUND: Many new diagnostic biomarkers have been developed for hepatocellular carcinoma (HCC). We selected two methods with high diagnostic value, the detection of serum microRNAs and metabolomics based on gas chromatography/mass spectrometry (GC/MS), and attempted to establish appropriate model...

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Autores principales: Liu, Hai-Ning, Wu, Hao, Chen, Yan-Jie, Tseng, Yu-Jen, Bilegsaikhan, Enkhnaran, Dong, Ling, Shen, Xi-Zhong, Liu, Tao-Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752483/
https://www.ncbi.nlm.nih.gov/pubmed/29312570
http://dx.doi.org/10.18632/oncotarget.22224
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author Liu, Hai-Ning
Wu, Hao
Chen, Yan-Jie
Tseng, Yu-Jen
Bilegsaikhan, Enkhnaran
Dong, Ling
Shen, Xi-Zhong
Liu, Tao-Tao
author_facet Liu, Hai-Ning
Wu, Hao
Chen, Yan-Jie
Tseng, Yu-Jen
Bilegsaikhan, Enkhnaran
Dong, Ling
Shen, Xi-Zhong
Liu, Tao-Tao
author_sort Liu, Hai-Ning
collection PubMed
description BACKGROUND: Many new diagnostic biomarkers have been developed for hepatocellular carcinoma (HCC). We selected two methods with high diagnostic value, the detection of serum microRNAs and metabolomics based on gas chromatography/mass spectrometry (GC/MS), and attempted to establish appropriate models. METHODS: We reviewed the diagnostic efficiencies of all microRNAs identified by previous diagnostic tests. Then we chose appropriate microRNAs to validate the diagnostic efficiencies, and determined the optimal combination. We included 66 patients with HCC and 82 healthy controls (HCs) and detected the expression of the microRNAs. GC/MS analysis was performed, and we used three multivariate statistical methods to establish diagnostic models. The concentration of alpha feto-protein (AFP) was determined for comparison with the novel models. RESULTS: 82 published studies and 92 microRNAs were ultimately included in this systematic review. Seven microRNAs were selected for further validation of their diagnostic efficiencies. Among which, miR-21, miR-106b, miR-125b, miR-182 and miR-224 had a significantly different expression in HCC patients. The combination of miR-21, miR-106b and miR-224 had the highest area under the curve (AUC) at 0.950 with a sensitivity of 80.3% and a specificity of 92.7%. The GC/MS analysis exhibited an excellent diagnostic value and the AUC reached 1.0. In comparison, the AUC of the traditional biomarker, AFP, was 0.755. CONCLUSION: MicroRNAs and metabolomics shows promising potential as new diagnostic methods due to their high diagnostic value compared with traditional biomarkers.
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spelling pubmed-57524832018-01-08 Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma Liu, Hai-Ning Wu, Hao Chen, Yan-Jie Tseng, Yu-Jen Bilegsaikhan, Enkhnaran Dong, Ling Shen, Xi-Zhong Liu, Tao-Tao Oncotarget Research Paper BACKGROUND: Many new diagnostic biomarkers have been developed for hepatocellular carcinoma (HCC). We selected two methods with high diagnostic value, the detection of serum microRNAs and metabolomics based on gas chromatography/mass spectrometry (GC/MS), and attempted to establish appropriate models. METHODS: We reviewed the diagnostic efficiencies of all microRNAs identified by previous diagnostic tests. Then we chose appropriate microRNAs to validate the diagnostic efficiencies, and determined the optimal combination. We included 66 patients with HCC and 82 healthy controls (HCs) and detected the expression of the microRNAs. GC/MS analysis was performed, and we used three multivariate statistical methods to establish diagnostic models. The concentration of alpha feto-protein (AFP) was determined for comparison with the novel models. RESULTS: 82 published studies and 92 microRNAs were ultimately included in this systematic review. Seven microRNAs were selected for further validation of their diagnostic efficiencies. Among which, miR-21, miR-106b, miR-125b, miR-182 and miR-224 had a significantly different expression in HCC patients. The combination of miR-21, miR-106b and miR-224 had the highest area under the curve (AUC) at 0.950 with a sensitivity of 80.3% and a specificity of 92.7%. The GC/MS analysis exhibited an excellent diagnostic value and the AUC reached 1.0. In comparison, the AUC of the traditional biomarker, AFP, was 0.755. CONCLUSION: MicroRNAs and metabolomics shows promising potential as new diagnostic methods due to their high diagnostic value compared with traditional biomarkers. Impact Journals LLC 2017-11-01 /pmc/articles/PMC5752483/ /pubmed/29312570 http://dx.doi.org/10.18632/oncotarget.22224 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Hai-Ning
Wu, Hao
Chen, Yan-Jie
Tseng, Yu-Jen
Bilegsaikhan, Enkhnaran
Dong, Ling
Shen, Xi-Zhong
Liu, Tao-Tao
Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title_full Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title_fullStr Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title_full_unstemmed Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title_short Serum microRNA signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
title_sort serum microrna signatures and metabolomics have high diagnostic value in hepatocellular carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752483/
https://www.ncbi.nlm.nih.gov/pubmed/29312570
http://dx.doi.org/10.18632/oncotarget.22224
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