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Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis

Rapid and efficient methods for the determination of cured tuberculosis (TB) are lacking. A total of 85 differentially expressed serum proteins were identified by iTRAQ labeling coupled with two-dimensional liquid chromatography-tandem mass spectrometry (2D LC-MS/MS) analysis (fold change >1.50 o...

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Autores principales: Wang, Chong, Wei, Li-Liang, Shi, Li-Ying, Pan, Zhi-Fen, Yu, Xiao-Mei, Li, Tian-Yu, Liu, Chang-Ming, Ping, Ze-Peng, Jiang, Ting-Ting, Chen, Zhong-Liang, Mao, Lian-Gen, Li, Zhong-Jie, Li, Ji-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620482/
https://www.ncbi.nlm.nih.gov/pubmed/26499913
http://dx.doi.org/10.1038/srep15615
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author Wang, Chong
Wei, Li-Liang
Shi, Li-Ying
Pan, Zhi-Fen
Yu, Xiao-Mei
Li, Tian-Yu
Liu, Chang-Ming
Ping, Ze-Peng
Jiang, Ting-Ting
Chen, Zhong-Liang
Mao, Lian-Gen
Li, Zhong-Jie
Li, Ji-Cheng
author_facet Wang, Chong
Wei, Li-Liang
Shi, Li-Ying
Pan, Zhi-Fen
Yu, Xiao-Mei
Li, Tian-Yu
Liu, Chang-Ming
Ping, Ze-Peng
Jiang, Ting-Ting
Chen, Zhong-Liang
Mao, Lian-Gen
Li, Zhong-Jie
Li, Ji-Cheng
author_sort Wang, Chong
collection PubMed
description Rapid and efficient methods for the determination of cured tuberculosis (TB) are lacking. A total of 85 differentially expressed serum proteins were identified by iTRAQ labeling coupled with two-dimensional liquid chromatography-tandem mass spectrometry (2D LC-MS/MS) analysis (fold change >1.50 or <0.60, P < 0.05). We validated albumin (ALB), Rho GDP-dissociation inhibitor 2 (ARHGDIB), complement 3 (C3), ficolin-2 (FCN2), and apolipoprotein (a) (LPA) using the enzyme-linked immunosorbent assay (ELISA) method. Significantly increased ALB and LPA levels (P = 0.036 and P = 0.012, respectively) and significantly reduced ARHGDIB, C3, and FCN2 levels (P < 0.001, P = 0.035, and P = 0.018, respectively) were observed in cured TB patients compared with untreated TB patients. In addition, changes in ALB and FCN2 levels occurred after 2 months of treatment (P < 0.001 and P = 0.030, respectively). We established a cured TB model with 87.10% sensitivity, 79.49% specificity, and an area under the curve (AUC) of 0.876. The results indicated that ALB, ARHGDIB, C3, FCN2, and LPA levels might serve as potential biomarkers for cured TB. Our study provides experimental data for establishing objective indicators of cured TB and also proposes potential markers for evaluating the efficacy of anti-TB drugs.
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spelling pubmed-46204822015-10-29 Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis Wang, Chong Wei, Li-Liang Shi, Li-Ying Pan, Zhi-Fen Yu, Xiao-Mei Li, Tian-Yu Liu, Chang-Ming Ping, Ze-Peng Jiang, Ting-Ting Chen, Zhong-Liang Mao, Lian-Gen Li, Zhong-Jie Li, Ji-Cheng Sci Rep Article Rapid and efficient methods for the determination of cured tuberculosis (TB) are lacking. A total of 85 differentially expressed serum proteins were identified by iTRAQ labeling coupled with two-dimensional liquid chromatography-tandem mass spectrometry (2D LC-MS/MS) analysis (fold change >1.50 or <0.60, P < 0.05). We validated albumin (ALB), Rho GDP-dissociation inhibitor 2 (ARHGDIB), complement 3 (C3), ficolin-2 (FCN2), and apolipoprotein (a) (LPA) using the enzyme-linked immunosorbent assay (ELISA) method. Significantly increased ALB and LPA levels (P = 0.036 and P = 0.012, respectively) and significantly reduced ARHGDIB, C3, and FCN2 levels (P < 0.001, P = 0.035, and P = 0.018, respectively) were observed in cured TB patients compared with untreated TB patients. In addition, changes in ALB and FCN2 levels occurred after 2 months of treatment (P < 0.001 and P = 0.030, respectively). We established a cured TB model with 87.10% sensitivity, 79.49% specificity, and an area under the curve (AUC) of 0.876. The results indicated that ALB, ARHGDIB, C3, FCN2, and LPA levels might serve as potential biomarkers for cured TB. Our study provides experimental data for establishing objective indicators of cured TB and also proposes potential markers for evaluating the efficacy of anti-TB drugs. Nature Publishing Group 2015-10-26 /pmc/articles/PMC4620482/ /pubmed/26499913 http://dx.doi.org/10.1038/srep15615 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Chong
Wei, Li-Liang
Shi, Li-Ying
Pan, Zhi-Fen
Yu, Xiao-Mei
Li, Tian-Yu
Liu, Chang-Ming
Ping, Ze-Peng
Jiang, Ting-Ting
Chen, Zhong-Liang
Mao, Lian-Gen
Li, Zhong-Jie
Li, Ji-Cheng
Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title_full Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title_fullStr Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title_full_unstemmed Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title_short Screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
title_sort screening and identification of five serum proteins as novel potential biomarkers for cured pulmonary tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4620482/
https://www.ncbi.nlm.nih.gov/pubmed/26499913
http://dx.doi.org/10.1038/srep15615
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