Treating Metastatic Brain Cancers With Stem Cells
Descripción del Articulo
Stem cell therapy may present an effective treatment for metastatic brain cancer and glioblastoma. Here we posit the critical role of a leaky blood-brain barrier (BBB) as a key element for the development of brain metastases, specifically melanoma. By reviewing the immunological and inflammatory res...
Autores: | , , , , , , , , , , , , , , , |
---|---|
Formato: | artículo |
Fecha de Publicación: | 2021 |
Institución: | Universidad Peruana de Ciencias Aplicadas |
Repositorio: | UPC-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/658440 |
Enlace del recurso: | http://hdl.handle.net/10757/658440 |
Nivel de acceso: | acceso abierto |
Materia: | blood brain barrier bone marrow derived mesenchymal stem cell brain metastases endothelial progenitor cell melanoma neuroinflammation stem cell therapy |
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dc.title.es_PE.fl_str_mv |
Treating Metastatic Brain Cancers With Stem Cells |
title |
Treating Metastatic Brain Cancers With Stem Cells |
spellingShingle |
Treating Metastatic Brain Cancers With Stem Cells Sadanandan, Nadia blood brain barrier bone marrow derived mesenchymal stem cell brain metastases endothelial progenitor cell melanoma neuroinflammation stem cell therapy |
title_short |
Treating Metastatic Brain Cancers With Stem Cells |
title_full |
Treating Metastatic Brain Cancers With Stem Cells |
title_fullStr |
Treating Metastatic Brain Cancers With Stem Cells |
title_full_unstemmed |
Treating Metastatic Brain Cancers With Stem Cells |
title_sort |
Treating Metastatic Brain Cancers With Stem Cells |
author |
Sadanandan, Nadia |
author_facet |
Sadanandan, Nadia Shear, Alex Brooks, Beverly Saft, Madeline Cabantan, Dorothy Anne Galang Kingsbury, Chase Zhang, Henry Anthony, Stefan Wang, Zhen Jie Salazar, Felipe Esparza Lezama Toledo, Alma R. Rivera Monroy, Germán Vega Gonzales-Portillo, Joaquin Moscatello, Alexa Lee, Jea Young Borlongan, Cesario V. |
author_role |
author |
author2 |
Shear, Alex Brooks, Beverly Saft, Madeline Cabantan, Dorothy Anne Galang Kingsbury, Chase Zhang, Henry Anthony, Stefan Wang, Zhen Jie Salazar, Felipe Esparza Lezama Toledo, Alma R. Rivera Monroy, Germán Vega Gonzales-Portillo, Joaquin Moscatello, Alexa Lee, Jea Young Borlongan, Cesario V. |
author2_role |
author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Sadanandan, Nadia Shear, Alex Brooks, Beverly Saft, Madeline Cabantan, Dorothy Anne Galang Kingsbury, Chase Zhang, Henry Anthony, Stefan Wang, Zhen Jie Salazar, Felipe Esparza Lezama Toledo, Alma R. Rivera Monroy, Germán Vega Gonzales-Portillo, Joaquin Moscatello, Alexa Lee, Jea Young Borlongan, Cesario V. |
dc.subject.es_PE.fl_str_mv |
blood brain barrier bone marrow derived mesenchymal stem cell brain metastases endothelial progenitor cell melanoma neuroinflammation stem cell therapy |
topic |
blood brain barrier bone marrow derived mesenchymal stem cell brain metastases endothelial progenitor cell melanoma neuroinflammation stem cell therapy |
description |
Stem cell therapy may present an effective treatment for metastatic brain cancer and glioblastoma. Here we posit the critical role of a leaky blood-brain barrier (BBB) as a key element for the development of brain metastases, specifically melanoma. By reviewing the immunological and inflammatory responses associated with BBB damage secondary to tumoral activity, we identify the involvement of this pathological process in the growth and formation of metastatic brain cancers. Likewise, we evaluate the hypothesis of regenerating impaired endothelial cells of the BBB and alleviating the damaged neurovascular unit to attenuate brain metastasis, using the endothelial progenitor cell (EPC) phenotype of bone marrow-derived mesenchymal stem cells. Specifically, there is a need to evaluate the efficacy for stem cell therapy to repair disruptions in the BBB and reduce inflammation in the brain, thereby causing attenuation of metastatic brain cancers. To establish the viability of stem cell therapy for the prevention and treatment of metastatic brain tumors, it is crucial to demonstrate BBB repair through augmentation of vasculogenesis and angiogenesis. BBB disruption is strongly linked to metastatic melanoma, worsens neuroinflammation during metastasis, and negatively influences the prognosis of metastatic brain cancer. Using stem cell therapy to interrupt inflammation secondary to this leaky BBB represents a paradigm-shifting approach for brain cancer treatment. In this review article, we critically assess the advantages and disadvantages of using stem cell therapy for brain metastases and glioblastoma. |
publishDate |
2021 |
dc.date.accessioned.none.fl_str_mv |
2022-01-04T15:36:41Z |
dc.date.available.none.fl_str_mv |
2022-01-04T15:36:41Z |
dc.date.issued.fl_str_mv |
2021-11-24 |
dc.type.es_PE.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
dc.identifier.issn.none.fl_str_mv |
16625099 |
dc.identifier.doi.none.fl_str_mv |
10.3389/fnmol.2021.749716 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10757/658440 |
dc.identifier.journal.es_PE.fl_str_mv |
Frontiers in Molecular Neuroscience |
dc.identifier.eid.none.fl_str_mv |
2-s2.0-85120911475 |
dc.identifier.scopusid.none.fl_str_mv |
SCOPUS_ID:85120911475 |
dc.identifier.isni.none.fl_str_mv |
0000 0001 2196 144X |
identifier_str_mv |
16625099 10.3389/fnmol.2021.749716 Frontiers in Molecular Neuroscience 2-s2.0-85120911475 SCOPUS_ID:85120911475 0000 0001 2196 144X |
url |
http://hdl.handle.net/10757/658440 |
dc.language.iso.es_PE.fl_str_mv |
eng |
language |
eng |
dc.relation.url.es_PE.fl_str_mv |
https://www.frontiersin.org/articles/10.3389/fnmol.2021.749716/full |
dc.rights.es_PE.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.*.fl_str_mv |
Attribution-NonCommercial-ShareAlike 4.0 International |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ |
dc.format.es_PE.fl_str_mv |
application/pdf |
dc.publisher.es_PE.fl_str_mv |
Frontiers Media S.A. |
dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Academico - UPC |
dc.source.none.fl_str_mv |
reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
instname_str |
Universidad Peruana de Ciencias Aplicadas |
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UPC |
institution |
UPC |
reponame_str |
UPC-Institucional |
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UPC-Institucional |
dc.source.journaltitle.none.fl_str_mv |
Frontiers in Molecular Neuroscience |
dc.source.volume.none.fl_str_mv |
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Here we posit the critical role of a leaky blood-brain barrier (BBB) as a key element for the development of brain metastases, specifically melanoma. By reviewing the immunological and inflammatory responses associated with BBB damage secondary to tumoral activity, we identify the involvement of this pathological process in the growth and formation of metastatic brain cancers. Likewise, we evaluate the hypothesis of regenerating impaired endothelial cells of the BBB and alleviating the damaged neurovascular unit to attenuate brain metastasis, using the endothelial progenitor cell (EPC) phenotype of bone marrow-derived mesenchymal stem cells. Specifically, there is a need to evaluate the efficacy for stem cell therapy to repair disruptions in the BBB and reduce inflammation in the brain, thereby causing attenuation of metastatic brain cancers. To establish the viability of stem cell therapy for the prevention and treatment of metastatic brain tumors, it is crucial to demonstrate BBB repair through augmentation of vasculogenesis and angiogenesis. BBB disruption is strongly linked to metastatic melanoma, worsens neuroinflammation during metastasis, and negatively influences the prognosis of metastatic brain cancer. Using stem cell therapy to interrupt inflammation secondary to this leaky BBB represents a paradigm-shifting approach for brain cancer treatment. 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Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).