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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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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. |
format | Online Article Text |
id | pubmed-5660227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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