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Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique

Tengfu Jiangya Tablet (TJT) is a well accepted antihypertension drug in China and its major active components were Uncaria total alkaloids and Semen Raphani soluble alkaloid. To further explore treatment effects mechanism of TJT on essential hypertension, a serum proteomic study was performed. Poten...

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Autores principales: Xu, Jingwen, Li, Yunlun, Zhang, Shijun, Jiang, Haiqiang, Wang, Nan, Lin, Haiqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376940/
https://www.ncbi.nlm.nih.gov/pubmed/28408942
http://dx.doi.org/10.1155/2017/7594805
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author Xu, Jingwen
Li, Yunlun
Zhang, Shijun
Jiang, Haiqiang
Wang, Nan
Lin, Haiqing
author_facet Xu, Jingwen
Li, Yunlun
Zhang, Shijun
Jiang, Haiqiang
Wang, Nan
Lin, Haiqing
author_sort Xu, Jingwen
collection PubMed
description Tengfu Jiangya Tablet (TJT) is a well accepted antihypertension drug in China and its major active components were Uncaria total alkaloids and Semen Raphani soluble alkaloid. To further explore treatment effects mechanism of TJT on essential hypertension, a serum proteomic study was performed. Potential biomarkers were quantified in serum of hypertension individuals before and after taking TJT with isobaric tags for relative and absolute quantitation (iTRAQ) coupled two-dimensional liquid chromatography followed electrospray ionization-tandem mass spectrometry (2D LC-MS/MS) proteomics technique. Among 391 identified proteins with high confidence, 70 proteins were differentially expressed (fold variation criteria, >1.2 or <0.83) between two groups (39 upregulated and 31 downregulated). Combining with Gene Ontology annotation, KEGG pathway analysis, and literature retrieval, 5 proteins were chosen as key target biomarkers during TJT therapeutic process. And the alteration profiles of these 5 proteins were verified by ELISA and Western Blot. Proteins Kininogen 1 and Keratin 1 are members of Kallikrein system, while Myeloperoxidase, Serum Amyloid protein A, and Retinol binding protein 4 had been reported closely related to vascular endothelial injury. Our study discovered 5 target biomarkers of the compound Chinese medicine TJT. Secondly, this research initially revealed the antihypertension therapeutic mechanism of this drug from a brand-new aspect.
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spelling pubmed-53769402017-04-13 Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique Xu, Jingwen Li, Yunlun Zhang, Shijun Jiang, Haiqiang Wang, Nan Lin, Haiqing Evid Based Complement Alternat Med Research Article Tengfu Jiangya Tablet (TJT) is a well accepted antihypertension drug in China and its major active components were Uncaria total alkaloids and Semen Raphani soluble alkaloid. To further explore treatment effects mechanism of TJT on essential hypertension, a serum proteomic study was performed. Potential biomarkers were quantified in serum of hypertension individuals before and after taking TJT with isobaric tags for relative and absolute quantitation (iTRAQ) coupled two-dimensional liquid chromatography followed electrospray ionization-tandem mass spectrometry (2D LC-MS/MS) proteomics technique. Among 391 identified proteins with high confidence, 70 proteins were differentially expressed (fold variation criteria, >1.2 or <0.83) between two groups (39 upregulated and 31 downregulated). Combining with Gene Ontology annotation, KEGG pathway analysis, and literature retrieval, 5 proteins were chosen as key target biomarkers during TJT therapeutic process. And the alteration profiles of these 5 proteins were verified by ELISA and Western Blot. Proteins Kininogen 1 and Keratin 1 are members of Kallikrein system, while Myeloperoxidase, Serum Amyloid protein A, and Retinol binding protein 4 had been reported closely related to vascular endothelial injury. Our study discovered 5 target biomarkers of the compound Chinese medicine TJT. Secondly, this research initially revealed the antihypertension therapeutic mechanism of this drug from a brand-new aspect. Hindawi 2017 2017-03-20 /pmc/articles/PMC5376940/ /pubmed/28408942 http://dx.doi.org/10.1155/2017/7594805 Text en Copyright © 2017 Jingwen Xu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Xu, Jingwen
Li, Yunlun
Zhang, Shijun
Jiang, Haiqiang
Wang, Nan
Lin, Haiqing
Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title_full Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title_fullStr Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title_full_unstemmed Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title_short Identification of Tengfu Jiangya Tablet Target Biomarkers with Quantitative Proteomic Technique
title_sort identification of tengfu jiangya tablet target biomarkers with quantitative proteomic technique
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376940/
https://www.ncbi.nlm.nih.gov/pubmed/28408942
http://dx.doi.org/10.1155/2017/7594805
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