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Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target?
This study was designed to investigate whether the Notch pathway is involved in the development of diffuse spinal cord astrocytomas. BALB/c nude mice received injections of CD133(+) and CD133(−) cell suspensions prepared using human recurrent diffuse spinal cord astrocytoma tissue through administra...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392672/ https://www.ncbi.nlm.nih.gov/pubmed/25883623 http://dx.doi.org/10.4103/1673-5374.152378 |
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author | Sun, Jian-jun Wang, Zhen-yu Li, Ling-song Yu, Hai-yan Xu, Yong-sheng Wu, Hai-bo Luo, Yi Liu, Bin Zheng, Mei Mao, Jin-long Lou, Xiao-hui |
author_facet | Sun, Jian-jun Wang, Zhen-yu Li, Ling-song Yu, Hai-yan Xu, Yong-sheng Wu, Hai-bo Luo, Yi Liu, Bin Zheng, Mei Mao, Jin-long Lou, Xiao-hui |
author_sort | Sun, Jian-jun |
collection | PubMed |
description | This study was designed to investigate whether the Notch pathway is involved in the development of diffuse spinal cord astrocytomas. BALB/c nude mice received injections of CD133(+) and CD133(−) cell suspensions prepared using human recurrent diffuse spinal cord astrocytoma tissue through administration into the right parietal lobe. After 7–11 weeks, magnetic resonance imaging was performed weekly. Xenografts were observed on the surfaces of the brains of mice receiving the CD133(+) cell suspension, and Notch-immunopositive expression was observed in the xenografts. By contrast, no xenografts appeared in the identical position on the surfaces of the brains of mice receiving the CD133(−) cell suspension, and Notch-immunopositive expression was hardly detected either. Hematoxylin-eosin staining and immunohistochemical staining revealed xenografts on the convex surfaces of the brains of mice that underwent CD133(+) astrocytoma transplantation. Some sporadic astroglioma cells showed pseudopodium-like structures, which extended into the cerebral white matter. However, it should be emphasized that the subcortex xenograft with Notch-immunopositive expression was found in the fourth mouse received injection of CD133(−) astrocytoma cells. However, these findings suggest that the Notch pathway plays an important role in the formation of astrocytomas, and can be considered a novel treatment target for diffuse spinal cord astrocytoma. |
format | Online Article Text |
id | pubmed-4392672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43926722015-04-16 Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? Sun, Jian-jun Wang, Zhen-yu Li, Ling-song Yu, Hai-yan Xu, Yong-sheng Wu, Hai-bo Luo, Yi Liu, Bin Zheng, Mei Mao, Jin-long Lou, Xiao-hui Neural Regen Res Research Article This study was designed to investigate whether the Notch pathway is involved in the development of diffuse spinal cord astrocytomas. BALB/c nude mice received injections of CD133(+) and CD133(−) cell suspensions prepared using human recurrent diffuse spinal cord astrocytoma tissue through administration into the right parietal lobe. After 7–11 weeks, magnetic resonance imaging was performed weekly. Xenografts were observed on the surfaces of the brains of mice receiving the CD133(+) cell suspension, and Notch-immunopositive expression was observed in the xenografts. By contrast, no xenografts appeared in the identical position on the surfaces of the brains of mice receiving the CD133(−) cell suspension, and Notch-immunopositive expression was hardly detected either. Hematoxylin-eosin staining and immunohistochemical staining revealed xenografts on the convex surfaces of the brains of mice that underwent CD133(+) astrocytoma transplantation. Some sporadic astroglioma cells showed pseudopodium-like structures, which extended into the cerebral white matter. However, it should be emphasized that the subcortex xenograft with Notch-immunopositive expression was found in the fourth mouse received injection of CD133(−) astrocytoma cells. However, these findings suggest that the Notch pathway plays an important role in the formation of astrocytomas, and can be considered a novel treatment target for diffuse spinal cord astrocytoma. Medknow Publications & Media Pvt Ltd 2015-02 /pmc/articles/PMC4392672/ /pubmed/25883623 http://dx.doi.org/10.4103/1673-5374.152378 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sun, Jian-jun Wang, Zhen-yu Li, Ling-song Yu, Hai-yan Xu, Yong-sheng Wu, Hai-bo Luo, Yi Liu, Bin Zheng, Mei Mao, Jin-long Lou, Xiao-hui Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title | Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title_full | Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title_fullStr | Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title_full_unstemmed | Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title_short | Prevention against diffuse spinal cord astrocytoma: can the Notch pathway be a novel treatment target? |
title_sort | prevention against diffuse spinal cord astrocytoma: can the notch pathway be a novel treatment target? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392672/ https://www.ncbi.nlm.nih.gov/pubmed/25883623 http://dx.doi.org/10.4103/1673-5374.152378 |
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