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Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas
Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678608/ https://www.ncbi.nlm.nih.gov/pubmed/33235631 http://dx.doi.org/10.3892/etm.2020.9454 |
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author | Liang, Chen Shangguan, Jian Yang, Ling Guo, Shiwen |
author_facet | Liang, Chen Shangguan, Jian Yang, Ling Guo, Shiwen |
author_sort | Liang, Chen |
collection | PubMed |
description | Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression. |
format | Online Article Text |
id | pubmed-7678608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-76786082020-11-23 Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas Liang, Chen Shangguan, Jian Yang, Ling Guo, Shiwen Exp Ther Med Articles Vasculogenic mimicry (VM) contributes to the resistance of anti-angiogenic therapies in glioma. Certain genes, including MMP-2 and VEGF may be associated with the development of VM. Astrocyte elevated gene-1 (AEG-1) is considered to be an oncogene that promotes autophagy, invasion, metastasis, angiogenesis and drug resistance; however, the association between AEG-1 and VM formation is still unknown. The present study investigated the effects of AEG-1 downregulation on VM formation in the U87 glioma cell line in vitro and in xenograft models of glioma, and the potential underlying mechanisms of action. In the present study, U87 glioma cells were infected with the AEG-1 short hairpin RNA lentivirus. A Matrigel-based tube formation assay was performed to evaluate VM formation in vitro. Reverse transcription-quantitative PCR and western blot analysis were conducted to investigate the mRNA and protein expression levels of MMP-2 and VEGF. Glioma xenograft models were generated through the intracerebral implantation of U87 glioma cells into nude rats; CD34/Periodic Acid-Schiff double-staining was performed to detect VM channels in vivo. Following AEG-1 downregulation in U87 cells, the development of VM was significantly decreased in vitro and in vivo. In addition, the expression levels of MMP-2 and VEGF in glioma cells were decreased compared with the control group. These results suggested that downregulation of AEG-1 expression could significantly inhibit the development of VM in gliomas, both in vitro and in vivo, and may be partially related to the regulation of VEGF and MMP-2 expression. D.A. Spandidos 2021-01 2020-11-06 /pmc/articles/PMC7678608/ /pubmed/33235631 http://dx.doi.org/10.3892/etm.2020.9454 Text en Copyright: © Liang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Liang, Chen Shangguan, Jian Yang, Ling Guo, Shiwen Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title_full | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title_fullStr | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title_full_unstemmed | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title_short | Downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
title_sort | downregulation of astrocyte elevated gene-1 expression inhibits the development of vasculogenic mimicry in gliomas |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7678608/ https://www.ncbi.nlm.nih.gov/pubmed/33235631 http://dx.doi.org/10.3892/etm.2020.9454 |
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