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Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach

Colorectal cancer (CRC) is a common malignant neoplasm worldwide. It is important to identify new biomarkers for the early detection of CRC. In this study, magnetic beads and the Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) platform were used to analyse...

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Autores principales: Yu, Jiekai, Zhai, Xiaohui, Li, Xiaofen, Zhong, Chenhan, Guo, Cheng, Yang, Fuquan, Yuan, Ying, Zheng, Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660227/
https://www.ncbi.nlm.nih.gov/pubmed/29079854
http://dx.doi.org/10.1038/s41598-017-14539-x
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author Yu, Jiekai
Zhai, Xiaohui
Li, Xiaofen
Zhong, Chenhan
Guo, Cheng
Yang, Fuquan
Yuan, Ying
Zheng, Shu
author_facet Yu, Jiekai
Zhai, Xiaohui
Li, Xiaofen
Zhong, Chenhan
Guo, Cheng
Yang, Fuquan
Yuan, Ying
Zheng, Shu
author_sort Yu, Jiekai
collection PubMed
description Colorectal cancer (CRC) is a common malignant neoplasm worldwide. It is important to identify new biomarkers for the early detection of CRC. In this study, magnetic beads and the Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) platform were used to analyse CRC and healthy control (HC) serum samples. The CRC diagnosis pattern was established to have a specificity of 94.7% and sensitivity of 92.3% in a blind test. The candidate biomarker serine/threonine kinase 4 (STK4, also known as MST1) was identified by Tandem mass spectrometry (MS/MS) and verified with western blotting and enzyme-linked immunosorbent assay (ELISA). The results indicated that there was a higher concentration of MST1 in HC subjects than stage I CRC patients for the early detection of CRC and a lower concentration in stage IV patients than in other CRC patients. The sensitivity and specificity of MST1 combined with carcinoembryonic antigen (CEA) and faecal occult blood test (FOBT) in diagnosis of colorectal cancer were 92.3% and 100%, respectively. Additionally, low MST1 expression was associated with the poor prognosis. These results illustrate that MST1 is a potential biomarker for early detection, prognosis and prediction of distant metastasis of CRC.
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spelling pubmed-56602272017-11-01 Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach Yu, Jiekai Zhai, Xiaohui Li, Xiaofen Zhong, Chenhan Guo, Cheng Yang, Fuquan Yuan, Ying Zheng, Shu Sci Rep Article Colorectal cancer (CRC) is a common malignant neoplasm worldwide. It is important to identify new biomarkers for the early detection of CRC. In this study, magnetic beads and the Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) platform were used to analyse CRC and healthy control (HC) serum samples. The CRC diagnosis pattern was established to have a specificity of 94.7% and sensitivity of 92.3% in a blind test. The candidate biomarker serine/threonine kinase 4 (STK4, also known as MST1) was identified by Tandem mass spectrometry (MS/MS) and verified with western blotting and enzyme-linked immunosorbent assay (ELISA). The results indicated that there was a higher concentration of MST1 in HC subjects than stage I CRC patients for the early detection of CRC and a lower concentration in stage IV patients than in other CRC patients. The sensitivity and specificity of MST1 combined with carcinoembryonic antigen (CEA) and faecal occult blood test (FOBT) in diagnosis of colorectal cancer were 92.3% and 100%, respectively. Additionally, low MST1 expression was associated with the poor prognosis. These results illustrate that MST1 is a potential biomarker for early detection, prognosis and prediction of distant metastasis of CRC. Nature Publishing Group UK 2017-10-27 /pmc/articles/PMC5660227/ /pubmed/29079854 http://dx.doi.org/10.1038/s41598-017-14539-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yu, Jiekai
Zhai, Xiaohui
Li, Xiaofen
Zhong, Chenhan
Guo, Cheng
Yang, Fuquan
Yuan, Ying
Zheng, Shu
Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title_full Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title_fullStr Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title_full_unstemmed Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title_short Identification of MST1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
title_sort identification of mst1 as a potential early detection biomarker for colorectal cancer through a proteomic approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5660227/
https://www.ncbi.nlm.nih.gov/pubmed/29079854
http://dx.doi.org/10.1038/s41598-017-14539-x
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