Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses

Detalhes bibliográficos
Autor(a) principal: Morrot, Alexandre
Data de Publicação: 2018
Outros Autores: Fonseca, Leonardo Marques da, Salustiano, Eduardo J., Gentile, Luciana Boffoni, Conde, Luciana, Filardy, Alessandra Almeida, Franklim, Tatiany Nunes, Costa, Kelly Monteiro da, Lima, Celio Geraldo Freire de, Lima, Leonardo Freire de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/31217
Resumo: Universidade Federal do Rio de Janeiro. Faculdade de Medicina. Rio de Janeiro, RJ, Brasil / Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunoparasitologia. Rio de Janeiro, RJ, Brasil.
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spelling Morrot, AlexandreFonseca, Leonardo Marques daSalustiano, Eduardo J.Gentile, Luciana BoffoniConde, LucianaFilardy, Alessandra AlmeidaFranklim, Tatiany NunesCosta, Kelly Monteiro daLima, Celio Geraldo Freire deLima, Leonardo Freire de2019-01-22T13:37:20Z2019-01-22T13:37:20Z2018MORROT, Alexandre; et al. Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses. Frontiers im Oncology, v.8, Article 81, 10p, Mar. 2018.2234-943Xhttps://www.arca.fiocruz.br/handle/icict/3121710.3389/fonc.2018.00081engFrontiers MediaCâncerMetabolismoCitocinasLactatoEvasão da Resposta ImuneCancerMetabolismLactateImmune evasionCytokinesEvasão da Resposta ImuneMetabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responsesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleUniversidade Federal do Rio de Janeiro. Faculdade de Medicina. Rio de Janeiro, RJ, Brasil / Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunoparasitologia. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Microbiologia. Departamento de Imunologia. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Microbiologia. Departamento de Imunologia. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.Universidade Federal do Rio de Janeiro. Instituto de Biofísica Carlos Chagas Filho. Rio de Janeiro, RJ, Brasil.The tumor microenvironment (TME) is composed by cellular and non-cellular components. Examples include the following: (i) bone marrow-derived inflammatory cells, (ii) fibroblasts, (iii) blood vessels, (iv) immune cells, and (v) extracellular matrix components. In most cases, this combination of components may result in an inhospitable environment, in which a significant retrenchment in nutrients and oxygen considerably disturbs cell metabolism. Cancer cells are characterized by an enhanced uptake and utilization of glucose, a phenomenon described by Otto Warburg over 90 years ago. One of the main products of this reprogrammed cell metabolism is lactate. “Lactagenic” or lactate-producing cancer cells are characterized by their immunomodulatory properties, since lactate, the end product of the aerobic glycolysis, besides acting as an inducer of cellular signaling phenomena to influence cellular fate, might also play a role as an immunosuppressive metabolite. Over the last 10 years, it has been well accepted that in the TME, the lactate secreted by transformed cells is able to compromise the function and/or assembly of an effective immune response against tumors. Herein, we will discuss recent advances regarding the deleterious effect of high concentrations of lactate on the tumor-infiltrating immune cells, which might characterize an innovative way of understanding the tumor-immune privilege.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/31217/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALalexandre_morrot_etal_IOC_2018.pdfalexandre_morrot_etal_IOC_2018.pdfapplication/pdf947912https://www.arca.fiocruz.br/bitstream/icict/31217/2/alexandre_morrot_etal_IOC_2018.pdf30d1bfb802eefd37d84a2ec58eda44d7MD52TEXTalexandre_morrot_etal_IOC_2018.pdf.txtalexandre_morrot_etal_IOC_2018.pdf.txtExtracted 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dc.title.pt_BR.fl_str_mv Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
title Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
spellingShingle Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
Morrot, Alexandre
Câncer
Metabolismo
Citocinas
Lactato
Evasão da Resposta Imune
Cancer
Metabolism
Lactate
Immune evasion
Cytokines
Evasão da Resposta Imune
title_short Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
title_full Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
title_fullStr Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
title_full_unstemmed Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
title_sort Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses
author Morrot, Alexandre
author_facet Morrot, Alexandre
Fonseca, Leonardo Marques da
Salustiano, Eduardo J.
Gentile, Luciana Boffoni
Conde, Luciana
Filardy, Alessandra Almeida
Franklim, Tatiany Nunes
Costa, Kelly Monteiro da
Lima, Celio Geraldo Freire de
Lima, Leonardo Freire de
author_role author
author2 Fonseca, Leonardo Marques da
Salustiano, Eduardo J.
Gentile, Luciana Boffoni
Conde, Luciana
Filardy, Alessandra Almeida
Franklim, Tatiany Nunes
Costa, Kelly Monteiro da
Lima, Celio Geraldo Freire de
Lima, Leonardo Freire de
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Morrot, Alexandre
Fonseca, Leonardo Marques da
Salustiano, Eduardo J.
Gentile, Luciana Boffoni
Conde, Luciana
Filardy, Alessandra Almeida
Franklim, Tatiany Nunes
Costa, Kelly Monteiro da
Lima, Celio Geraldo Freire de
Lima, Leonardo Freire de
dc.subject.other.pt_BR.fl_str_mv Câncer
Metabolismo
Citocinas
Lactato
Evasão da Resposta Imune
topic Câncer
Metabolismo
Citocinas
Lactato
Evasão da Resposta Imune
Cancer
Metabolism
Lactate
Immune evasion
Cytokines
Evasão da Resposta Imune
dc.subject.en.pt_BR.fl_str_mv Cancer
Metabolism
Lactate
Immune evasion
Cytokines
dc.subject.decs.pt_BR.fl_str_mv Evasão da Resposta Imune
description Universidade Federal do Rio de Janeiro. Faculdade de Medicina. Rio de Janeiro, RJ, Brasil / Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunoparasitologia. Rio de Janeiro, RJ, Brasil.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2019-01-22T13:37:20Z
dc.date.available.fl_str_mv 2019-01-22T13:37:20Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv MORROT, Alexandre; et al. Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses. Frontiers im Oncology, v.8, Article 81, 10p, Mar. 2018.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/31217
dc.identifier.issn.pt_BR.fl_str_mv 2234-943X
dc.identifier.doi.none.fl_str_mv 10.3389/fonc.2018.00081
identifier_str_mv MORROT, Alexandre; et al. Metabolic Symbiosis and immunomodulation: How Tumor Cell-Derived Lactate May Disturb innate and Adaptive immune Responses. Frontiers im Oncology, v.8, Article 81, 10p, Mar. 2018.
2234-943X
10.3389/fonc.2018.00081
url https://www.arca.fiocruz.br/handle/icict/31217
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Frontiers Media
publisher.none.fl_str_mv Frontiers Media
dc.source.none.fl_str_mv reponame:Repositório Institucional da FIOCRUZ (ARCA)
instname:Fundação Oswaldo Cruz (FIOCRUZ)
instacron:FIOCRUZ
instname_str Fundação Oswaldo Cruz (FIOCRUZ)
instacron_str FIOCRUZ
institution FIOCRUZ
reponame_str Repositório Institucional da FIOCRUZ (ARCA)
collection Repositório Institucional da FIOCRUZ (ARCA)
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