Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/18388 |
Resumo: | INTRODUCTION: Astrocytic gliomas are the most common intracranial central nervous system neoplasias, accounting for about 60% of all primary central nervous system tumors. Despite advances in the treatment of gliomas, no effective therapeutic approach is yet available; hence, the search for a more realistic model to generate more effective therapies is essential. OBJECTIVE: To develop an experimental malignant astrocytoma model with the characteristics of the human tumor. METHOD: Primary cells from subcutaneous xenograft tumors produced with malignant astrocytoma U87MG cells were inoculated intracerebrally by stereotaxis into immunosuppressed (athymic) Rowett rats. RESULTS: All four injected animals developed non-infiltrative tumors, although other glioblastoma characteristics, such as necrosis, pseudopalisading cells and intense mitotic activity, were observed. CONCLUSION: A malignant astrocytoma intracerebral xenograft model with poorly invasive behavior was achieved in athymic Rowett rats. Tumor invasiveness in an experimental animal model may depend on a combination of several factors, including the cell line used to induce tumor formation, the rat strains and the status of the animal's immune system. |
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Clinics |
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Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma Brain tumorExperimental modelAthymic Rowett ratsU87MG cells INTRODUCTION: Astrocytic gliomas are the most common intracranial central nervous system neoplasias, accounting for about 60% of all primary central nervous system tumors. Despite advances in the treatment of gliomas, no effective therapeutic approach is yet available; hence, the search for a more realistic model to generate more effective therapies is essential. OBJECTIVE: To develop an experimental malignant astrocytoma model with the characteristics of the human tumor. METHOD: Primary cells from subcutaneous xenograft tumors produced with malignant astrocytoma U87MG cells were inoculated intracerebrally by stereotaxis into immunosuppressed (athymic) Rowett rats. RESULTS: All four injected animals developed non-infiltrative tumors, although other glioblastoma characteristics, such as necrosis, pseudopalisading cells and intense mitotic activity, were observed. CONCLUSION: A malignant astrocytoma intracerebral xenograft model with poorly invasive behavior was achieved in athymic Rowett rats. Tumor invasiveness in an experimental animal model may depend on a combination of several factors, including the cell line used to induce tumor formation, the rat strains and the status of the animal's immune system. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1838810.1590/S1807-59322010000300011Clinics; Vol. 65 No. 3 (2010); 305-309 Clinics; v. 65 n. 3 (2010); 305-309 Clinics; Vol. 65 Núm. 3 (2010); 305-309 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/18388/20451Miura, Flávio KeyAlves, Maria Jose FerreiraRocha, Mussya CisottoSilva, Roseli daOba-Shinjo, Sueli MiekoMarie, Suely Kazue Nagahashiinfo:eu-repo/semantics/openAccess2012-05-23T11:19:25Zoai:revistas.usp.br:article/18388Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T11:19:25Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
title |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
spellingShingle |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma Miura, Flávio Key Brain tumor Experimental model Athymic Rowett rats U87MG cells |
title_short |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
title_full |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
title_fullStr |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
title_full_unstemmed |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
title_sort |
Xenograft transplantation of human malignant astrocytoma cells into immunodeficient rats: an experimental model of glioblastoma |
author |
Miura, Flávio Key |
author_facet |
Miura, Flávio Key Alves, Maria Jose Ferreira Rocha, Mussya Cisotto Silva, Roseli da Oba-Shinjo, Sueli Mieko Marie, Suely Kazue Nagahashi |
author_role |
author |
author2 |
Alves, Maria Jose Ferreira Rocha, Mussya Cisotto Silva, Roseli da Oba-Shinjo, Sueli Mieko Marie, Suely Kazue Nagahashi |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Miura, Flávio Key Alves, Maria Jose Ferreira Rocha, Mussya Cisotto Silva, Roseli da Oba-Shinjo, Sueli Mieko Marie, Suely Kazue Nagahashi |
dc.subject.por.fl_str_mv |
Brain tumor Experimental model Athymic Rowett rats U87MG cells |
topic |
Brain tumor Experimental model Athymic Rowett rats U87MG cells |
description |
INTRODUCTION: Astrocytic gliomas are the most common intracranial central nervous system neoplasias, accounting for about 60% of all primary central nervous system tumors. Despite advances in the treatment of gliomas, no effective therapeutic approach is yet available; hence, the search for a more realistic model to generate more effective therapies is essential. OBJECTIVE: To develop an experimental malignant astrocytoma model with the characteristics of the human tumor. METHOD: Primary cells from subcutaneous xenograft tumors produced with malignant astrocytoma U87MG cells were inoculated intracerebrally by stereotaxis into immunosuppressed (athymic) Rowett rats. RESULTS: All four injected animals developed non-infiltrative tumors, although other glioblastoma characteristics, such as necrosis, pseudopalisading cells and intense mitotic activity, were observed. CONCLUSION: A malignant astrocytoma intracerebral xenograft model with poorly invasive behavior was achieved in athymic Rowett rats. Tumor invasiveness in an experimental animal model may depend on a combination of several factors, including the cell line used to induce tumor formation, the rat strains and the status of the animal's immune system. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/18388 10.1590/S1807-59322010000300011 |
url |
https://www.revistas.usp.br/clinics/article/view/18388 |
identifier_str_mv |
10.1590/S1807-59322010000300011 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/18388/20451 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 65 No. 3 (2010); 305-309 Clinics; v. 65 n. 3 (2010); 305-309 Clinics; Vol. 65 Núm. 3 (2010); 305-309 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222755255222272 |