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Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening
Matrix metalloproteinase-9 (MMP-9) is related to tumour development and progression in colorectal cancer (CRC) and its utility as biomarker has been suggested. The aim of our study was to measure serum MMP-9 in asymptomatic first-degree relatives of CRC patients, and to analyse its diagnostic accura...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532998/ https://www.ncbi.nlm.nih.gov/pubmed/26264519 http://dx.doi.org/10.1038/srep13030 |
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author | Otero-Estévez, Olalla Chiara, Loretta De Rodríguez-Girondo, Mar Rodríguez-Berrocal, Francisco Javier Cubiella, Joaquín Castro, Inés Hernández, Vicent Martínez-Zorzano, Vicenta Soledad |
author_facet | Otero-Estévez, Olalla Chiara, Loretta De Rodríguez-Girondo, Mar Rodríguez-Berrocal, Francisco Javier Cubiella, Joaquín Castro, Inés Hernández, Vicent Martínez-Zorzano, Vicenta Soledad |
author_sort | Otero-Estévez, Olalla |
collection | PubMed |
description | Matrix metalloproteinase-9 (MMP-9) is related to tumour development and progression in colorectal cancer (CRC) and its utility as biomarker has been suggested. The aim of our study was to measure serum MMP-9 in asymptomatic first-degree relatives of CRC patients, and to analyse its diagnostic accuracy for the detection of advanced neoplasia (AN: advanced adenomas and CRC). Additionally, we compared its diagnostic capability with the most used non-invasive faecal immunochemical test (FIT). Serum MMP-9 was quantified by ELISA in 516 asymptomatic individuals that underwent a colonoscopy and a FIT. MMP-9 levels were significantly related to age and gender and therefore the concentration was corrected by these confounders. Corrected MMP-9 (cMMP-9) levels were higher in individuals with advanced adenomas (AA; p-value = 0.029) and AN (p-value = 0.056) compared to individuals with no neoplasia. Moreover, elevated cMMP-9 concentration was associated with more severe characteristics of adenomas (number of lesions, size and histology). Nevertheless, the diagnostic accuracy of cMMP-9 was considerably lower than that of FIT for identifying AA (22.64% vs. 47.17% sensitivity, 90% specificity) or AN (19.30% vs. 52.63% sensitivity, 90% specificity). According to our results, serum MMP-9 cannot be considered of utility for the diagnosis of AN in CRC family-risk population screening. |
format | Online Article Text |
id | pubmed-4532998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45329982015-08-12 Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening Otero-Estévez, Olalla Chiara, Loretta De Rodríguez-Girondo, Mar Rodríguez-Berrocal, Francisco Javier Cubiella, Joaquín Castro, Inés Hernández, Vicent Martínez-Zorzano, Vicenta Soledad Sci Rep Article Matrix metalloproteinase-9 (MMP-9) is related to tumour development and progression in colorectal cancer (CRC) and its utility as biomarker has been suggested. The aim of our study was to measure serum MMP-9 in asymptomatic first-degree relatives of CRC patients, and to analyse its diagnostic accuracy for the detection of advanced neoplasia (AN: advanced adenomas and CRC). Additionally, we compared its diagnostic capability with the most used non-invasive faecal immunochemical test (FIT). Serum MMP-9 was quantified by ELISA in 516 asymptomatic individuals that underwent a colonoscopy and a FIT. MMP-9 levels were significantly related to age and gender and therefore the concentration was corrected by these confounders. Corrected MMP-9 (cMMP-9) levels were higher in individuals with advanced adenomas (AA; p-value = 0.029) and AN (p-value = 0.056) compared to individuals with no neoplasia. Moreover, elevated cMMP-9 concentration was associated with more severe characteristics of adenomas (number of lesions, size and histology). Nevertheless, the diagnostic accuracy of cMMP-9 was considerably lower than that of FIT for identifying AA (22.64% vs. 47.17% sensitivity, 90% specificity) or AN (19.30% vs. 52.63% sensitivity, 90% specificity). According to our results, serum MMP-9 cannot be considered of utility for the diagnosis of AN in CRC family-risk population screening. Nature Publishing Group 2015-08-12 /pmc/articles/PMC4532998/ /pubmed/26264519 http://dx.doi.org/10.1038/srep13030 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 Otero-Estévez, Olalla Chiara, Loretta De Rodríguez-Girondo, Mar Rodríguez-Berrocal, Francisco Javier Cubiella, Joaquín Castro, Inés Hernández, Vicent Martínez-Zorzano, Vicenta Soledad Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title | Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title_full | Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title_fullStr | Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title_full_unstemmed | Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title_short | Serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
title_sort | serum matrix metalloproteinase-9 in colorectal cancer family-risk population screening |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532998/ https://www.ncbi.nlm.nih.gov/pubmed/26264519 http://dx.doi.org/10.1038/srep13030 |
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