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Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells

INTRODUCTION: The presence of monocyte and macrophage cells in growing breast tumors, and the positive relationship between the degree of immune cell infiltration and tumor growth, suggest a possible paracrine growth regulatory function of immune cells in breast cancer. METHOD: To better understand...

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Detalles Bibliográficos
Autores principales: Szabo, Kristina A, Singh, Gurmit
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1242127/
https://www.ncbi.nlm.nih.gov/pubmed/16168111
http://dx.doi.org/10.1186/bcr1261
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author Szabo, Kristina A
Singh, Gurmit
author_facet Szabo, Kristina A
Singh, Gurmit
author_sort Szabo, Kristina A
collection PubMed
description INTRODUCTION: The presence of monocyte and macrophage cells in growing breast tumors, and the positive relationship between the degree of immune cell infiltration and tumor growth, suggest a possible paracrine growth regulatory function of immune cells in breast cancer. METHOD: To better understand the interaction between monocytes and breast cancer cells, in vitro matrix metalloproteinase and tissue inhibitor of metalloproteinase activity was assessed from the THP-1 myeloid cell line in response to conditioned media from two breast cancer cell lines, MCF-7 and MDA-MB-231. RESULTS: Enzymography and immunoblotting revealed increased MMP-2 as well as increased levels of TIMP-1 and TIMP-2. Furthermore, a significant increase in the invasive potential of MCF-7 and MDA-MB-231 cells was noted in response to THP-1 cell-conditioned media. CONCLUSION: These data demonstrate that monocyte cells in the breast tumor microenvironment play an important role in the modulation of MMPs, which may have a significant effect on the control of tumor growth and metastatic spread.
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spelling pubmed-12421272005-10-06 Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells Szabo, Kristina A Singh, Gurmit Breast Cancer Res Research Article INTRODUCTION: The presence of monocyte and macrophage cells in growing breast tumors, and the positive relationship between the degree of immune cell infiltration and tumor growth, suggest a possible paracrine growth regulatory function of immune cells in breast cancer. METHOD: To better understand the interaction between monocytes and breast cancer cells, in vitro matrix metalloproteinase and tissue inhibitor of metalloproteinase activity was assessed from the THP-1 myeloid cell line in response to conditioned media from two breast cancer cell lines, MCF-7 and MDA-MB-231. RESULTS: Enzymography and immunoblotting revealed increased MMP-2 as well as increased levels of TIMP-1 and TIMP-2. Furthermore, a significant increase in the invasive potential of MCF-7 and MDA-MB-231 cells was noted in response to THP-1 cell-conditioned media. CONCLUSION: These data demonstrate that monocyte cells in the breast tumor microenvironment play an important role in the modulation of MMPs, which may have a significant effect on the control of tumor growth and metastatic spread. BioMed Central 2005 2005-06-14 /pmc/articles/PMC1242127/ /pubmed/16168111 http://dx.doi.org/10.1186/bcr1261 Text en Copyright © 2005 Szabo et al.; licensee BioMed Central Ltd.
spellingShingle Research Article
Szabo, Kristina A
Singh, Gurmit
Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title_full Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title_fullStr Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title_full_unstemmed Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title_short Modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
title_sort modulation of monocyte matrix metalloproteinase-2 by breast adenocarcinoma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1242127/
https://www.ncbi.nlm.nih.gov/pubmed/16168111
http://dx.doi.org/10.1186/bcr1261
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