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ADAMTS Expression in Colorectal Cancer
ADAMTSs are a family of secreted proteinases that share the metalloproteinase domain with matrix metalloproteinases (MMPs). By acting on a large panel of extracellular substrates, they control several cell functions such as fusion, adhesion, proliferation and migration. Through their thrombospondin...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364768/ https://www.ncbi.nlm.nih.gov/pubmed/25786261 http://dx.doi.org/10.1371/journal.pone.0121209 |
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author | Filou, Serafula Korpetinou, Aggeliki Kyriakopoulou, Dora Bounias, Dimitrios Stavropoulos, Michael Ravazoula, Panagiota Papachristou, Dionysios J. Theocharis, Achilleas D. Vynios, Demitrios H. |
author_facet | Filou, Serafula Korpetinou, Aggeliki Kyriakopoulou, Dora Bounias, Dimitrios Stavropoulos, Michael Ravazoula, Panagiota Papachristou, Dionysios J. Theocharis, Achilleas D. Vynios, Demitrios H. |
author_sort | Filou, Serafula |
collection | PubMed |
description | ADAMTSs are a family of secreted proteinases that share the metalloproteinase domain with matrix metalloproteinases (MMPs). By acting on a large panel of extracellular substrates, they control several cell functions such as fusion, adhesion, proliferation and migration. Through their thrombospondin motifs they also possess anti-angiogenic properties. We investigated whether ADAMTSs participate in colorectal cancer progression and invasion. Their expression was investigated at both mRNA and protein levels. Using RT-PCR, the expression of ADAMTS-1, -4, -5 and ADAMTS-20 was estimated in colorectal tumors of different cancer stage and anatomic site and 3 cell lines of different aggressiveness. An overexpression of ADAMTS-4 and -5 was observed, especially in tissue samples, whereas ADAMTS-1 and -20 were found to be down-regulated. Western blot analysis further supported the RT-PCR findings, revealing in addition the degradation of ADAMTS-1 and -20 in cancer. In situ expression and localization of ADAMTS-1, -4, -5 and -20 was also investigated by immunohistochemical analysis. Our data suggest a positive correlation between ADAMTS-4 and -5 expression and cancer progression, in contrast with the anti-angiogenic members of the family, ADAMTS-1 and -20, which were found to be down-regulated. Our findings support the notion that overexpression of ADAMTS-4 and ADAMTS-5 in colorectal cancer might be a possible invasive mechanism of cancer cells in order to degrade proteoglycans of ECM. |
format | Online Article Text |
id | pubmed-4364768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43647682015-03-23 ADAMTS Expression in Colorectal Cancer Filou, Serafula Korpetinou, Aggeliki Kyriakopoulou, Dora Bounias, Dimitrios Stavropoulos, Michael Ravazoula, Panagiota Papachristou, Dionysios J. Theocharis, Achilleas D. Vynios, Demitrios H. PLoS One Research Article ADAMTSs are a family of secreted proteinases that share the metalloproteinase domain with matrix metalloproteinases (MMPs). By acting on a large panel of extracellular substrates, they control several cell functions such as fusion, adhesion, proliferation and migration. Through their thrombospondin motifs they also possess anti-angiogenic properties. We investigated whether ADAMTSs participate in colorectal cancer progression and invasion. Their expression was investigated at both mRNA and protein levels. Using RT-PCR, the expression of ADAMTS-1, -4, -5 and ADAMTS-20 was estimated in colorectal tumors of different cancer stage and anatomic site and 3 cell lines of different aggressiveness. An overexpression of ADAMTS-4 and -5 was observed, especially in tissue samples, whereas ADAMTS-1 and -20 were found to be down-regulated. Western blot analysis further supported the RT-PCR findings, revealing in addition the degradation of ADAMTS-1 and -20 in cancer. In situ expression and localization of ADAMTS-1, -4, -5 and -20 was also investigated by immunohistochemical analysis. Our data suggest a positive correlation between ADAMTS-4 and -5 expression and cancer progression, in contrast with the anti-angiogenic members of the family, ADAMTS-1 and -20, which were found to be down-regulated. Our findings support the notion that overexpression of ADAMTS-4 and ADAMTS-5 in colorectal cancer might be a possible invasive mechanism of cancer cells in order to degrade proteoglycans of ECM. Public Library of Science 2015-03-18 /pmc/articles/PMC4364768/ /pubmed/25786261 http://dx.doi.org/10.1371/journal.pone.0121209 Text en © 2015 Filou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Filou, Serafula Korpetinou, Aggeliki Kyriakopoulou, Dora Bounias, Dimitrios Stavropoulos, Michael Ravazoula, Panagiota Papachristou, Dionysios J. Theocharis, Achilleas D. Vynios, Demitrios H. ADAMTS Expression in Colorectal Cancer |
title | ADAMTS Expression in Colorectal Cancer |
title_full | ADAMTS Expression in Colorectal Cancer |
title_fullStr | ADAMTS Expression in Colorectal Cancer |
title_full_unstemmed | ADAMTS Expression in Colorectal Cancer |
title_short | ADAMTS Expression in Colorectal Cancer |
title_sort | adamts expression in colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4364768/ https://www.ncbi.nlm.nih.gov/pubmed/25786261 http://dx.doi.org/10.1371/journal.pone.0121209 |
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