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Study of matrix metalloproteinases and their inhibitors in breast cancer

An immunohistochemical study was performed using tissue microarrays and specific antibodies against matrix metalloproteinases (MMPs) 1, 2, 7, 9, 11, 13, 14, and their tisullar inhibitors (TIMPs) 1, 2, and 3. More than 2600 determinations on cancer specimens from 131 patients with primary ductal inva...

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Autores principales: Vizoso, F J, González, L O, Corte, M D, Rodríguez, J C, Vázquez, J, Lamelas, M L, Junquera, S, Merino, A M, García-Muñiz, J L
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360108/
https://www.ncbi.nlm.nih.gov/pubmed/17342087
http://dx.doi.org/10.1038/sj.bjc.6603666
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author Vizoso, F J
González, L O
Corte, M D
Rodríguez, J C
Vázquez, J
Lamelas, M L
Junquera, S
Merino, A M
García-Muñiz, J L
author_facet Vizoso, F J
González, L O
Corte, M D
Rodríguez, J C
Vázquez, J
Lamelas, M L
Junquera, S
Merino, A M
García-Muñiz, J L
author_sort Vizoso, F J
collection PubMed
description An immunohistochemical study was performed using tissue microarrays and specific antibodies against matrix metalloproteinases (MMPs) 1, 2, 7, 9, 11, 13, 14, and their tisullar inhibitors (TIMPs) 1, 2, and 3. More than 2600 determinations on cancer specimens from 131 patients with primary ductal invasive tumours of the breast (65 with and 66 without distant metastasis) and controls were performed. Staining results were categorised using a score based on the intensity of the staining and a specific software program calculated the percentage of immunostained cells automatically. We observed a broad variation of the total immunostaining scores and the cell type expressing each protein. There were multiple and significant associations between the expression of the different MMPs and TIMPs evaluated and some parameters indicative of tumour aggressiveness, such as large tumour size, advanced tumour grade, high Nottinham prognostic index, negative oestrogen receptor status, peritumoural inflammation, desmoplastic reaction, and infiltrating tumoural edge. Likewise, the detection of elevated immunohistochemical scores for MMP-9, 11, TIMP-1, and TIMP-2, was significantly associated with a higher rate of distant metastases. The expression of MMP-9 or TIMP-2 by tumour cells, MMP-1, 7, 9, 11, 13, or TIMP-3 by fibroblastic cells, and MMP-7, 9, 11, 13, 14, TIMP-1, or TIMP-2 by mononuclear inflammatory cells, was also significantly associated with a higher rate of distant metastases.
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spelling pubmed-23601082009-09-10 Study of matrix metalloproteinases and their inhibitors in breast cancer Vizoso, F J González, L O Corte, M D Rodríguez, J C Vázquez, J Lamelas, M L Junquera, S Merino, A M García-Muñiz, J L Br J Cancer Clinical Study An immunohistochemical study was performed using tissue microarrays and specific antibodies against matrix metalloproteinases (MMPs) 1, 2, 7, 9, 11, 13, 14, and their tisullar inhibitors (TIMPs) 1, 2, and 3. More than 2600 determinations on cancer specimens from 131 patients with primary ductal invasive tumours of the breast (65 with and 66 without distant metastasis) and controls were performed. Staining results were categorised using a score based on the intensity of the staining and a specific software program calculated the percentage of immunostained cells automatically. We observed a broad variation of the total immunostaining scores and the cell type expressing each protein. There were multiple and significant associations between the expression of the different MMPs and TIMPs evaluated and some parameters indicative of tumour aggressiveness, such as large tumour size, advanced tumour grade, high Nottinham prognostic index, negative oestrogen receptor status, peritumoural inflammation, desmoplastic reaction, and infiltrating tumoural edge. Likewise, the detection of elevated immunohistochemical scores for MMP-9, 11, TIMP-1, and TIMP-2, was significantly associated with a higher rate of distant metastases. The expression of MMP-9 or TIMP-2 by tumour cells, MMP-1, 7, 9, 11, 13, or TIMP-3 by fibroblastic cells, and MMP-7, 9, 11, 13, 14, TIMP-1, or TIMP-2 by mononuclear inflammatory cells, was also significantly associated with a higher rate of distant metastases. Nature Publishing Group 2007-03-26 2007-03-06 /pmc/articles/PMC2360108/ /pubmed/17342087 http://dx.doi.org/10.1038/sj.bjc.6603666 Text en Copyright © 2007 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 Clinical Study
Vizoso, F J
González, L O
Corte, M D
Rodríguez, J C
Vázquez, J
Lamelas, M L
Junquera, S
Merino, A M
García-Muñiz, J L
Study of matrix metalloproteinases and their inhibitors in breast cancer
title Study of matrix metalloproteinases and their inhibitors in breast cancer
title_full Study of matrix metalloproteinases and their inhibitors in breast cancer
title_fullStr Study of matrix metalloproteinases and their inhibitors in breast cancer
title_full_unstemmed Study of matrix metalloproteinases and their inhibitors in breast cancer
title_short Study of matrix metalloproteinases and their inhibitors in breast cancer
title_sort study of matrix metalloproteinases and their inhibitors in breast cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360108/
https://www.ncbi.nlm.nih.gov/pubmed/17342087
http://dx.doi.org/10.1038/sj.bjc.6603666
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