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Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics

BACKGROUND: The average 5-year survival rate of lung adenocarcinoma patients is only 15% to 17%, which is primarily due to late-stage diagnosis and a lack of specific prognostic evaluations that can recommend effective therapies. Additionally, there is no clinically recognized biomarker that is effe...

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Autores principales: Mo, Liang, Wei, Bing, Liang, Renji, Yang, Zhi, Xie, Shouzhi, Wu, Shengrong, You, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177994/
https://www.ncbi.nlm.nih.gov/pubmed/32316791
http://dx.doi.org/10.1177/0300060519897215
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author Mo, Liang
Wei, Bing
Liang, Renji
Yang, Zhi
Xie, Shouzhi
Wu, Shengrong
You, Yong
author_facet Mo, Liang
Wei, Bing
Liang, Renji
Yang, Zhi
Xie, Shouzhi
Wu, Shengrong
You, Yong
author_sort Mo, Liang
collection PubMed
description BACKGROUND: The average 5-year survival rate of lung adenocarcinoma patients is only 15% to 17%, which is primarily due to late-stage diagnosis and a lack of specific prognostic evaluations that can recommend effective therapies. Additionally, there is no clinically recognized biomarker that is effective for early-stage diagnosis. METHODS: Tissue samples from 10 lung adenocarcinoma patients (both tumor and non-tumor tissues) and 10 benign lung tumor samples were collected. The significantly differentially represented metabolites from the three groups were analyzed by liquid chromatography and tandem mass spectrometry. RESULTS: Pathway analysis indicated that central carbon metabolism was the top altered pathway in lung adenocarcinoma, while protein digestion and absorption, and central carbon metabolism were the top altered pathways in benign lung tumors. Receiver operating characteristic curve analysis revealed that adenosine 3′-monophosphate, creatine, glycerol, and 14 other differential metabolites were potential sensitive and specific biomarkers for the diagnosis and prognosis of lung adenocarcinoma. CONCLUSION: Our findings suggest that the metabolomics approach may be a useful method to detect potential biomarkers in lung adenocarcinoma patients.
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spelling pubmed-71779942020-05-01 Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics Mo, Liang Wei, Bing Liang, Renji Yang, Zhi Xie, Shouzhi Wu, Shengrong You, Yong J Int Med Res Retrospective Clinical Research Report BACKGROUND: The average 5-year survival rate of lung adenocarcinoma patients is only 15% to 17%, which is primarily due to late-stage diagnosis and a lack of specific prognostic evaluations that can recommend effective therapies. Additionally, there is no clinically recognized biomarker that is effective for early-stage diagnosis. METHODS: Tissue samples from 10 lung adenocarcinoma patients (both tumor and non-tumor tissues) and 10 benign lung tumor samples were collected. The significantly differentially represented metabolites from the three groups were analyzed by liquid chromatography and tandem mass spectrometry. RESULTS: Pathway analysis indicated that central carbon metabolism was the top altered pathway in lung adenocarcinoma, while protein digestion and absorption, and central carbon metabolism were the top altered pathways in benign lung tumors. Receiver operating characteristic curve analysis revealed that adenosine 3′-monophosphate, creatine, glycerol, and 14 other differential metabolites were potential sensitive and specific biomarkers for the diagnosis and prognosis of lung adenocarcinoma. CONCLUSION: Our findings suggest that the metabolomics approach may be a useful method to detect potential biomarkers in lung adenocarcinoma patients. SAGE Publications 2020-04-22 /pmc/articles/PMC7177994/ /pubmed/32316791 http://dx.doi.org/10.1177/0300060519897215 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Mo, Liang
Wei, Bing
Liang, Renji
Yang, Zhi
Xie, Shouzhi
Wu, Shengrong
You, Yong
Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title_full Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title_fullStr Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title_full_unstemmed Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title_short Exploring potential biomarkers for lung adenocarcinoma using LC-MS/MS metabolomics
title_sort exploring potential biomarkers for lung adenocarcinoma using lc-ms/ms metabolomics
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7177994/
https://www.ncbi.nlm.nih.gov/pubmed/32316791
http://dx.doi.org/10.1177/0300060519897215
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