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The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer
Several members of the human tissue kallikrein-related peptidase (KLK) family are emerging cancer biomarkers. The aim of this study was to analyse the expression of a panel of KLKs in colorectal cancer and to find out if the multiparametric combination of them can increase the accuracy of prediction...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696752/ https://www.ncbi.nlm.nih.gov/pubmed/19367279 http://dx.doi.org/10.1038/sj.bjc.6605033 |
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author | Talieri, M Li, L Zheng, Y Alexopoulou, D K Soosaipillai, A Scorilas, A Xynopoulos, D Diamandis, E P |
author_facet | Talieri, M Li, L Zheng, Y Alexopoulou, D K Soosaipillai, A Scorilas, A Xynopoulos, D Diamandis, E P |
author_sort | Talieri, M |
collection | PubMed |
description | Several members of the human tissue kallikrein-related peptidase (KLK) family are emerging cancer biomarkers. The aim of this study was to analyse the expression of a panel of KLKs in colorectal cancer and to find out if the multiparametric combination of them can increase the accuracy of prediction of patients survival beyond the traditional clinical information. Nine KLKs (KLK5-8, KLK10, KLK11, KLK13-15) were measured using ELISA assays in cytosolic extracts of 122 colon cancer tissues and their nearby normal mucosa, obtained during surgery. The mean levels of almost all KLKs in tumour tissues were significantly different from their counterparts of normal tissue (P<0.0001). KLK 5, 6, 7, 13, 14 were significantly associated with overall survival in univariate analysis, but after adjusting for age, TNM and differentiation stage, only KLK5 (HR: 1.24 (95% CI: 1.05–1.47)), KLK7 (HR: 1.57 (95% CI: 1.04–2.37)) and KLK14 (HR: 1.43 (95% CI: 1.05–1.94)) remained significant. Addition of a panel of selected KLK markers to clinical parameters gave an increment in AUC of 0.86 beyond the clinical factors at year 1, showing that it can increase the accuracy of prediction of overall survival beyond the traditional clinical information, particularly the short-term (1 year) survival after surgery. |
format | Text |
id | pubmed-2696752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-26967522010-05-19 The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer Talieri, M Li, L Zheng, Y Alexopoulou, D K Soosaipillai, A Scorilas, A Xynopoulos, D Diamandis, E P Br J Cancer Molecular Diagnostics Several members of the human tissue kallikrein-related peptidase (KLK) family are emerging cancer biomarkers. The aim of this study was to analyse the expression of a panel of KLKs in colorectal cancer and to find out if the multiparametric combination of them can increase the accuracy of prediction of patients survival beyond the traditional clinical information. Nine KLKs (KLK5-8, KLK10, KLK11, KLK13-15) were measured using ELISA assays in cytosolic extracts of 122 colon cancer tissues and their nearby normal mucosa, obtained during surgery. The mean levels of almost all KLKs in tumour tissues were significantly different from their counterparts of normal tissue (P<0.0001). KLK 5, 6, 7, 13, 14 were significantly associated with overall survival in univariate analysis, but after adjusting for age, TNM and differentiation stage, only KLK5 (HR: 1.24 (95% CI: 1.05–1.47)), KLK7 (HR: 1.57 (95% CI: 1.04–2.37)) and KLK14 (HR: 1.43 (95% CI: 1.05–1.94)) remained significant. Addition of a panel of selected KLK markers to clinical parameters gave an increment in AUC of 0.86 beyond the clinical factors at year 1, showing that it can increase the accuracy of prediction of overall survival beyond the traditional clinical information, particularly the short-term (1 year) survival after surgery. Nature Publishing Group 2009-05-19 2009-04-14 /pmc/articles/PMC2696752/ /pubmed/19367279 http://dx.doi.org/10.1038/sj.bjc.6605033 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Talieri, M Li, L Zheng, Y Alexopoulou, D K Soosaipillai, A Scorilas, A Xynopoulos, D Diamandis, E P The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title | The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title_full | The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title_fullStr | The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title_full_unstemmed | The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title_short | The use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
title_sort | use of kallikrein-related peptidases as adjuvant prognostic markers in colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2696752/ https://www.ncbi.nlm.nih.gov/pubmed/19367279 http://dx.doi.org/10.1038/sj.bjc.6605033 |
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