Treating Metastatic Brain Cancers With Stem Cells

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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...

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Detalles Bibliográficos
Autores: 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.
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
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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
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identifier_str_mv 16625099
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Frontiers in Molecular Neuroscience
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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
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eu_rights_str_mv openAccess
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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
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instname_str Universidad Peruana de Ciencias Aplicadas
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institution UPC
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dc.source.journaltitle.none.fl_str_mv Frontiers in Molecular Neuroscience
dc.source.volume.none.fl_str_mv 14
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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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