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Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells

OBJECTIVE: The new glioma cell line SHG-139 was established and its phenotype, tumorigenicity, pathological characteristics, derived stem cells SHG139S were studied. METHODS: Immunohistochemistry was used to assess expressions in the patient and mouse tumor tissues, SHG-139 and SHG-139S. Primary SHG...

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Autores principales: Li, Yanyan, Wang, Hangzhou, Sun, Ting, Chen, Jinming, Guo, Lingchuan, Shen, Haitao, Du, Ziwei, Zhou, Youxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392480/
https://www.ncbi.nlm.nih.gov/pubmed/25879429
http://dx.doi.org/10.1186/s12943-015-0343-z
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author Li, Yanyan
Wang, Hangzhou
Sun, Ting
Chen, Jinming
Guo, Lingchuan
Shen, Haitao
Du, Ziwei
Zhou, Youxin
author_facet Li, Yanyan
Wang, Hangzhou
Sun, Ting
Chen, Jinming
Guo, Lingchuan
Shen, Haitao
Du, Ziwei
Zhou, Youxin
author_sort Li, Yanyan
collection PubMed
description OBJECTIVE: The new glioma cell line SHG-139 was established and its phenotype, tumorigenicity, pathological characteristics, derived stem cells SHG139S were studied. METHODS: Immunohistochemistry was used to assess expressions in the patient and mouse tumor tissues, SHG-139 and SHG-139S. Primary SHG-139 culture was performed, cell proliferation, cell cycle and genetic characteristics were assessed. MiRNA (Micro RNA) and LncRNA (Long non-coding RNA) microarray was performed. RESULTS: We found that the glioma tissue was positive for A2B5 (Glial precursors ganglioside), GFAP (Glial fibrillary acidic protein), S-100 (Acid calcium bingding protein), VEGF (Vascular endothelial growth factor), VEGFR (Vascular endothelial growth factor receptor) and negative for Ki-67 (Nuclcar- associated antigen). SHG-139 proliferated significantly within 24h; its total number of chromosomes was 68; ratios of SHG-139 and SHG-139S cells in G1 phase were highest. SHG-139 cells were positive for A2B5, GalC (Galactocerebrosides), GFAP, S-100 and Vimentin, while SHG-139S cells were positive for A2B5, Nestin, and NG2 (Neuron-glia antigen2), and negative for Vimentin and IDHR132H (Isocitrate dehydrogenase); cells rarely stained for CD133 (Cluster of differentiation133). SHG-139 intracranial xenografts expressed GFAP, but no overt oligodendroglioma was observed. In SHG-139S xenografts, GFAP and S-100 were expressed, while CD133 was not detected; a few A2B5(+) cells were found at tumor edges, and typical oligodendroglioma were obtained. In addition, SHG-139S xenograft tumors were more aggressive than those of SHG-139. Anti-mouse CD31 (Cluster of differentiation31) staining revealed murine vessels at the border between xenograft tumor and normal brain tissue; Anti-human CD34 (Cluster of differentiation34) staining was negative. Biochip technology of SHG139S showed several miRNA and lncRNA were differently expressed in SHG139 and SHG139S. CONCLUSIONS: SHG-139 was an astroglioma cell line which yielded stem cells SHG-139S. SHG-139S cells constituted an A2B5(+)/CD133(−) GSC subgroup. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-015-0343-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-43924802015-04-11 Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells Li, Yanyan Wang, Hangzhou Sun, Ting Chen, Jinming Guo, Lingchuan Shen, Haitao Du, Ziwei Zhou, Youxin Mol Cancer Research OBJECTIVE: The new glioma cell line SHG-139 was established and its phenotype, tumorigenicity, pathological characteristics, derived stem cells SHG139S were studied. METHODS: Immunohistochemistry was used to assess expressions in the patient and mouse tumor tissues, SHG-139 and SHG-139S. Primary SHG-139 culture was performed, cell proliferation, cell cycle and genetic characteristics were assessed. MiRNA (Micro RNA) and LncRNA (Long non-coding RNA) microarray was performed. RESULTS: We found that the glioma tissue was positive for A2B5 (Glial precursors ganglioside), GFAP (Glial fibrillary acidic protein), S-100 (Acid calcium bingding protein), VEGF (Vascular endothelial growth factor), VEGFR (Vascular endothelial growth factor receptor) and negative for Ki-67 (Nuclcar- associated antigen). SHG-139 proliferated significantly within 24h; its total number of chromosomes was 68; ratios of SHG-139 and SHG-139S cells in G1 phase were highest. SHG-139 cells were positive for A2B5, GalC (Galactocerebrosides), GFAP, S-100 and Vimentin, while SHG-139S cells were positive for A2B5, Nestin, and NG2 (Neuron-glia antigen2), and negative for Vimentin and IDHR132H (Isocitrate dehydrogenase); cells rarely stained for CD133 (Cluster of differentiation133). SHG-139 intracranial xenografts expressed GFAP, but no overt oligodendroglioma was observed. In SHG-139S xenografts, GFAP and S-100 were expressed, while CD133 was not detected; a few A2B5(+) cells were found at tumor edges, and typical oligodendroglioma were obtained. In addition, SHG-139S xenograft tumors were more aggressive than those of SHG-139. Anti-mouse CD31 (Cluster of differentiation31) staining revealed murine vessels at the border between xenograft tumor and normal brain tissue; Anti-human CD34 (Cluster of differentiation34) staining was negative. Biochip technology of SHG139S showed several miRNA and lncRNA were differently expressed in SHG139 and SHG139S. CONCLUSIONS: SHG-139 was an astroglioma cell line which yielded stem cells SHG-139S. SHG-139S cells constituted an A2B5(+)/CD133(−) GSC subgroup. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12943-015-0343-z) contains supplementary material, which is available to authorized users. BioMed Central 2015-04-02 /pmc/articles/PMC4392480/ /pubmed/25879429 http://dx.doi.org/10.1186/s12943-015-0343-z Text en © Li et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Yanyan
Wang, Hangzhou
Sun, Ting
Chen, Jinming
Guo, Lingchuan
Shen, Haitao
Du, Ziwei
Zhou, Youxin
Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title_full Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title_fullStr Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title_full_unstemmed Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title_short Biological characteristics of a new human glioma cell line transformed into A2B5(+) stem cells
title_sort biological characteristics of a new human glioma cell line transformed into a2b5(+) stem cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392480/
https://www.ncbi.nlm.nih.gov/pubmed/25879429
http://dx.doi.org/10.1186/s12943-015-0343-z
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