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Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells

BACKGROUND: The constitutive overexpression of matrix metalloproteinases (MMPs) is frequently observed in malignant tumours. In particular, MMP-2 and MMP-9 have been reported to be closely associated with invasion and angiogenesis in malignant gliomas. Our study aimed to evaluate the antitumour effe...

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Autores principales: Nakabayashi, Hiromichi, Yawata, Toshio, Shimizu, Keiji
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909207/
https://www.ncbi.nlm.nih.gov/pubmed/20587068
http://dx.doi.org/10.1186/1471-2407-10-339
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author Nakabayashi, Hiromichi
Yawata, Toshio
Shimizu, Keiji
author_facet Nakabayashi, Hiromichi
Yawata, Toshio
Shimizu, Keiji
author_sort Nakabayashi, Hiromichi
collection PubMed
description BACKGROUND: The constitutive overexpression of matrix metalloproteinases (MMPs) is frequently observed in malignant tumours. In particular, MMP-2 and MMP-9 have been reported to be closely associated with invasion and angiogenesis in malignant gliomas. Our study aimed to evaluate the antitumour effects of MMI-166 (Nalpha-[4-(2-Phenyl-2H- tetrazole-5-yl) phenyl sulfonyl]-D-tryptophan), a third generation MMP inhibitor, on three human glioma cell lines (T98G, U87MG, and ONS12) in vitro and in vivo. METHODS: The effects of MMI-166 on the gelatinolytic activity was analysed by gelatine zymography. The anti-invasive effect of MMI-166 was analysed by an in vitro invasion assay. An in vitro angiogenesis assay was also performed. In vitro growth inhibition of glioma cells by MMI-166 was determined by the MTT assay. The effect of MMI-166 on an orthotropic implantation model using athymic mice was also evaluated. RESULTS: Gelatine zymography revealed that MMP-2 and MMP-9 activities were suppressed by MMI-166. The invasion of glioma cells was suppressed by MMI-166. The angiogenesis assay showed that MMI-166 had a suppressive effect on glioma cell-induced angiogenesis. However, MMI-166 did not suppress glioma cell proliferation in the MTT assay. In vivo, MMI-166 suppressed tumour growth in athymic mice implanted orthotropically with T98G cells and showed an inhibitory effect on tumour-induced angiogenesis and tumour growth. This is the first report of the effect of a third generation MMP inhibitor on malignant glioma cells. CONCLUSIONS: These results suggest that MMI-166 may have potentially suppressive effects on the invasion and angiogenesis of malignant gliomas.
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spelling pubmed-29092072010-07-24 Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells Nakabayashi, Hiromichi Yawata, Toshio Shimizu, Keiji BMC Cancer Research Article BACKGROUND: The constitutive overexpression of matrix metalloproteinases (MMPs) is frequently observed in malignant tumours. In particular, MMP-2 and MMP-9 have been reported to be closely associated with invasion and angiogenesis in malignant gliomas. Our study aimed to evaluate the antitumour effects of MMI-166 (Nalpha-[4-(2-Phenyl-2H- tetrazole-5-yl) phenyl sulfonyl]-D-tryptophan), a third generation MMP inhibitor, on three human glioma cell lines (T98G, U87MG, and ONS12) in vitro and in vivo. METHODS: The effects of MMI-166 on the gelatinolytic activity was analysed by gelatine zymography. The anti-invasive effect of MMI-166 was analysed by an in vitro invasion assay. An in vitro angiogenesis assay was also performed. In vitro growth inhibition of glioma cells by MMI-166 was determined by the MTT assay. The effect of MMI-166 on an orthotropic implantation model using athymic mice was also evaluated. RESULTS: Gelatine zymography revealed that MMP-2 and MMP-9 activities were suppressed by MMI-166. The invasion of glioma cells was suppressed by MMI-166. The angiogenesis assay showed that MMI-166 had a suppressive effect on glioma cell-induced angiogenesis. However, MMI-166 did not suppress glioma cell proliferation in the MTT assay. In vivo, MMI-166 suppressed tumour growth in athymic mice implanted orthotropically with T98G cells and showed an inhibitory effect on tumour-induced angiogenesis and tumour growth. This is the first report of the effect of a third generation MMP inhibitor on malignant glioma cells. CONCLUSIONS: These results suggest that MMI-166 may have potentially suppressive effects on the invasion and angiogenesis of malignant gliomas. BioMed Central 2010-06-29 /pmc/articles/PMC2909207/ /pubmed/20587068 http://dx.doi.org/10.1186/1471-2407-10-339 Text en Copyright ©2010 Nakabayashi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nakabayashi, Hiromichi
Yawata, Toshio
Shimizu, Keiji
Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title_full Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title_fullStr Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title_full_unstemmed Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title_short Anti-invasive and antiangiogenic effects of MMI-166 on malignant glioma cells
title_sort anti-invasive and antiangiogenic effects of mmi-166 on malignant glioma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909207/
https://www.ncbi.nlm.nih.gov/pubmed/20587068
http://dx.doi.org/10.1186/1471-2407-10-339
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