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Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours.
The concentrations of cathepsin D (Cath D), urokinase (uPA) and two plasminogen activator inhibitors (PAI-1 and PAI-2) were analysed in the cytosols of 130 human mammary tumours (43 benign tumours and 87 primary and unilateral breast carcinomas). uPA, PAI-1 and PAI-2 levels were measured by antigeni...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977447/ https://www.ncbi.nlm.nih.gov/pubmed/1931618 |
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author | Foucré, D. Bouchet, C. Hacène, K. Pourreau-Schneider, N. Gentile, A. Martin, P. M. Desplaces, A. Oglobine, J. |
author_facet | Foucré, D. Bouchet, C. Hacène, K. Pourreau-Schneider, N. Gentile, A. Martin, P. M. Desplaces, A. Oglobine, J. |
author_sort | Foucré, D. |
collection | PubMed |
description | The concentrations of cathepsin D (Cath D), urokinase (uPA) and two plasminogen activator inhibitors (PAI-1 and PAI-2) were analysed in the cytosols of 130 human mammary tumours (43 benign tumours and 87 primary and unilateral breast carcinomas). uPA, PAI-1 and PAI-2 levels were measured by antigenic immunoassays and Cath D by immunoradiometric assay. The median levels of the four parameters were significantly higher in the malignant tumours than in the benign ones. Cath D and uPA increases were 4-fold and 5-fold respectively. PAI-1 and PAI-2 increases were much more important, 74-fold and 29-fold respectively. In malignant tumours, median levels of Cath D and uPA did not vary according to classical prognostic factors (histologic grade, presence or absence of axillary lymph nodes, steroid receptors, UICC stage, tumour size, age, and menopausal status). However, PAI-1 decreased in ER+ and PR+ tumours and PAI-2 increased in menopausal women's tumours. When Cath D, uPA, PAI-1 and PAI-2 levels in malignant tumours were compared, positive correlations were found for all combinations. The implication of plasminogen activator inhibitors in the phenomenon was surprising and merits further investigation using tools other than global antigen measurements in tumours. |
format | Text |
id | pubmed-1977447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19774472009-09-10 Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. Foucré, D. Bouchet, C. Hacène, K. Pourreau-Schneider, N. Gentile, A. Martin, P. M. Desplaces, A. Oglobine, J. Br J Cancer Research Article The concentrations of cathepsin D (Cath D), urokinase (uPA) and two plasminogen activator inhibitors (PAI-1 and PAI-2) were analysed in the cytosols of 130 human mammary tumours (43 benign tumours and 87 primary and unilateral breast carcinomas). uPA, PAI-1 and PAI-2 levels were measured by antigenic immunoassays and Cath D by immunoradiometric assay. The median levels of the four parameters were significantly higher in the malignant tumours than in the benign ones. Cath D and uPA increases were 4-fold and 5-fold respectively. PAI-1 and PAI-2 increases were much more important, 74-fold and 29-fold respectively. In malignant tumours, median levels of Cath D and uPA did not vary according to classical prognostic factors (histologic grade, presence or absence of axillary lymph nodes, steroid receptors, UICC stage, tumour size, age, and menopausal status). However, PAI-1 decreased in ER+ and PR+ tumours and PAI-2 increased in menopausal women's tumours. When Cath D, uPA, PAI-1 and PAI-2 levels in malignant tumours were compared, positive correlations were found for all combinations. The implication of plasminogen activator inhibitors in the phenomenon was surprising and merits further investigation using tools other than global antigen measurements in tumours. Nature Publishing Group 1991-11 /pmc/articles/PMC1977447/ /pubmed/1931618 Text en 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 | Research Article Foucré, D. Bouchet, C. Hacène, K. Pourreau-Schneider, N. Gentile, A. Martin, P. M. Desplaces, A. Oglobine, J. Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title | Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title_full | Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title_fullStr | Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title_full_unstemmed | Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title_short | Relationship between cathepsin D, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
title_sort | relationship between cathepsin d, urokinase, and plasminogen activator inhibitors in malignant vs benign breast tumours. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1977447/ https://www.ncbi.nlm.nih.gov/pubmed/1931618 |
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