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Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method

Bladder cancer (BC) is the second most prevalent malignancy in the urinary system and is associated with significant mortality; thus, there is an urgent need for novel noninvasive diagnostic biomarkers. A urinary pseudotargeted method based on gas chromatography–mass spectrometry was developed and v...

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Autores principales: Zhou, Yang, Song, Ruixiang, Ma, Chong, Zhou, Lina, Liu, Xinyu, Yin, Peiyuan, Zhang, Zhensheng, Sun, Yinghao, Xu, Chuanliang, Lu, Xin, Xu, Guowang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400539/
https://www.ncbi.nlm.nih.gov/pubmed/28157703
http://dx.doi.org/10.18632/oncotarget.14988
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author Zhou, Yang
Song, Ruixiang
Ma, Chong
Zhou, Lina
Liu, Xinyu
Yin, Peiyuan
Zhang, Zhensheng
Sun, Yinghao
Xu, Chuanliang
Lu, Xin
Xu, Guowang
author_facet Zhou, Yang
Song, Ruixiang
Ma, Chong
Zhou, Lina
Liu, Xinyu
Yin, Peiyuan
Zhang, Zhensheng
Sun, Yinghao
Xu, Chuanliang
Lu, Xin
Xu, Guowang
author_sort Zhou, Yang
collection PubMed
description Bladder cancer (BC) is the second most prevalent malignancy in the urinary system and is associated with significant mortality; thus, there is an urgent need for novel noninvasive diagnostic biomarkers. A urinary pseudotargeted method based on gas chromatography–mass spectrometry was developed and validated for a BC metabolomics study. The method exhibited good repeatability, intraday and interday precision, linearity and metabolome coverage. A total of 76 differential metabolites were defined in the discovery sample set, 58 of which were verified using an independent validation urine set. The verified differential metabolites revealed that energy metabolism, anabolic metabolism and cell redox states were disordered in BC. Based on a binary logistic regression analysis, a four-biomarker panel was defined for the diagnosis of BC. The area under the receiving operator characteristic curve was 0.885 with 88.0% sensitivity and 85.7% specificity in the discovery set and 0.804 with 78.0% sensitivity and 70.3% specificity in the validation set. The combinatorial biomarker panel was also useful for the early diagnosis of BC. This approach can be used to discriminate non-muscle invasive and low-grade BCs from healthy controls with satisfactory sensitivity and specificity. The results show that the developed urinary metabolomics method can be employed to effectively screen noninvasive biomarkers.
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spelling pubmed-54005392017-05-03 Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method Zhou, Yang Song, Ruixiang Ma, Chong Zhou, Lina Liu, Xinyu Yin, Peiyuan Zhang, Zhensheng Sun, Yinghao Xu, Chuanliang Lu, Xin Xu, Guowang Oncotarget Research Paper Bladder cancer (BC) is the second most prevalent malignancy in the urinary system and is associated with significant mortality; thus, there is an urgent need for novel noninvasive diagnostic biomarkers. A urinary pseudotargeted method based on gas chromatography–mass spectrometry was developed and validated for a BC metabolomics study. The method exhibited good repeatability, intraday and interday precision, linearity and metabolome coverage. A total of 76 differential metabolites were defined in the discovery sample set, 58 of which were verified using an independent validation urine set. The verified differential metabolites revealed that energy metabolism, anabolic metabolism and cell redox states were disordered in BC. Based on a binary logistic regression analysis, a four-biomarker panel was defined for the diagnosis of BC. The area under the receiving operator characteristic curve was 0.885 with 88.0% sensitivity and 85.7% specificity in the discovery set and 0.804 with 78.0% sensitivity and 70.3% specificity in the validation set. The combinatorial biomarker panel was also useful for the early diagnosis of BC. This approach can be used to discriminate non-muscle invasive and low-grade BCs from healthy controls with satisfactory sensitivity and specificity. The results show that the developed urinary metabolomics method can be employed to effectively screen noninvasive biomarkers. Impact Journals LLC 2017-02-01 /pmc/articles/PMC5400539/ /pubmed/28157703 http://dx.doi.org/10.18632/oncotarget.14988 Text en Copyright: © 2017 Zhou et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Zhou, Yang
Song, Ruixiang
Ma, Chong
Zhou, Lina
Liu, Xinyu
Yin, Peiyuan
Zhang, Zhensheng
Sun, Yinghao
Xu, Chuanliang
Lu, Xin
Xu, Guowang
Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title_full Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title_fullStr Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title_full_unstemmed Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title_short Discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted GC-MS metabolomics method
title_sort discovery and validation of potential urinary biomarkers for bladder cancer diagnosis using a pseudotargeted gc-ms metabolomics method
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5400539/
https://www.ncbi.nlm.nih.gov/pubmed/28157703
http://dx.doi.org/10.18632/oncotarget.14988
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