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Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer

A kinetic enzyme-linked immunosorbent assay (ELISA) for plasma tissue inhibitor of metalloproteinase (TIMP)-1 was developed in order to examine the potential diagnostic and prognostic value of TIMP-1 measurements in cancer patients. The ELISA enabled specific detection of total TIMP-1 in EDTA, citra...

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Autores principales: Holten-Andersen, M N, Murphy, G, Nielsen, H J, Pedersen, A N, Christensen, I J, Høyer-Hansen, G, Brünner, N, Stephens, R W
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362309/
https://www.ncbi.nlm.nih.gov/pubmed/10408859
http://dx.doi.org/10.1038/sj.bjc.6690384
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author Holten-Andersen, M N
Murphy, G
Nielsen, H J
Pedersen, A N
Christensen, I J
Høyer-Hansen, G
Brünner, N
Stephens, R W
author_facet Holten-Andersen, M N
Murphy, G
Nielsen, H J
Pedersen, A N
Christensen, I J
Høyer-Hansen, G
Brünner, N
Stephens, R W
author_sort Holten-Andersen, M N
collection PubMed
description A kinetic enzyme-linked immunosorbent assay (ELISA) for plasma tissue inhibitor of metalloproteinase (TIMP)-1 was developed in order to examine the potential diagnostic and prognostic value of TIMP-1 measurements in cancer patients. The ELISA enabled specific detection of total TIMP-1 in EDTA, citrate and heparin plasma. The assay was rigorously tested and requirements of sensitivity, specificity, stability and good recovery were fulfilled. TIMP-1 levels measured in citrate plasma (mean 69.2 ± 13.1 μg l(−1)) correlated with TIMP-1 measured in EDTA plasma (mean 73.5 ± 14.2 μg l(−1)) from the same individuals in a set of 100 healthy blood donors (Spearman's rho = 0.62, P < 0.0001). The mean level of TIMP-1 in EDTA plasma from 143 patients with Dukes' stage D colorectal cancer was 240 ± 145 μg l(−1) and a Mann–Whitney test demonstrated a highly significant difference between TIMP-1 levels in healthy blood donors and colorectal cancer patients (P < 0.0001). Similar findings were obtained for 19 patients with advanced breast cancer (mean 292 ± 331 μg l(−1)). The results show that TIMP-1 is readily measured in plasma samples by ELISA and that increased levels of TIMP-1 are found in patients with advanced cancer. It is proposed that plasma measurements of TIMP-1 may have value in the management of cancer patients. © 1999 Cancer Research Campaign
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spelling pubmed-23623092009-09-10 Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer Holten-Andersen, M N Murphy, G Nielsen, H J Pedersen, A N Christensen, I J Høyer-Hansen, G Brünner, N Stephens, R W Br J Cancer Regular Article A kinetic enzyme-linked immunosorbent assay (ELISA) for plasma tissue inhibitor of metalloproteinase (TIMP)-1 was developed in order to examine the potential diagnostic and prognostic value of TIMP-1 measurements in cancer patients. The ELISA enabled specific detection of total TIMP-1 in EDTA, citrate and heparin plasma. The assay was rigorously tested and requirements of sensitivity, specificity, stability and good recovery were fulfilled. TIMP-1 levels measured in citrate plasma (mean 69.2 ± 13.1 μg l(−1)) correlated with TIMP-1 measured in EDTA plasma (mean 73.5 ± 14.2 μg l(−1)) from the same individuals in a set of 100 healthy blood donors (Spearman's rho = 0.62, P < 0.0001). The mean level of TIMP-1 in EDTA plasma from 143 patients with Dukes' stage D colorectal cancer was 240 ± 145 μg l(−1) and a Mann–Whitney test demonstrated a highly significant difference between TIMP-1 levels in healthy blood donors and colorectal cancer patients (P < 0.0001). Similar findings were obtained for 19 patients with advanced breast cancer (mean 292 ± 331 μg l(−1)). The results show that TIMP-1 is readily measured in plasma samples by ELISA and that increased levels of TIMP-1 are found in patients with advanced cancer. It is proposed that plasma measurements of TIMP-1 may have value in the management of cancer patients. © 1999 Cancer Research Campaign Nature Publishing Group 1999-05 1999-05-01 /pmc/articles/PMC2362309/ /pubmed/10408859 http://dx.doi.org/10.1038/sj.bjc.6690384 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Holten-Andersen, M N
Murphy, G
Nielsen, H J
Pedersen, A N
Christensen, I J
Høyer-Hansen, G
Brünner, N
Stephens, R W
Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title_full Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title_fullStr Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title_full_unstemmed Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title_short Quantitation of TIMP-1 in plasma of healthy blood donors and patients with advanced cancer
title_sort quantitation of timp-1 in plasma of healthy blood donors and patients with advanced cancer
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362309/
https://www.ncbi.nlm.nih.gov/pubmed/10408859
http://dx.doi.org/10.1038/sj.bjc.6690384
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