Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments

Detalhes bibliográficos
Autor(a) principal: Vitorino, M
Data de Publicação: 2022
Outros Autores: Baptista de Almeida, S, Alpuim Costa, D, Faria, A, Calhau, C, Azambuja Braga, S
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.26/41551
Resumo: Breast cancer (BC) is the most common malignancy and the second cause of cancer-specific death in women from high-income countries. Infectious agents are the third most important risk factor for cancer incidence after tobacco and obesity. Dysbiosis emerged as a key player that may influence cancer development, treatment, and prognosis through diverse biological processes. Metastatic BC has a highly variable clinical course, and more recently, immune checkpoint inhibitors (ICIs) have become an emerging therapy in BC. Even with standardised treatment protocols, patients do not respond similarly, reflecting each individual´s heterogeneity, unique BC features, and tumour microenvironment. However, there is insufficient data regarding predictive factors of response to available treatments for BC. The microbiota could be a crucial piece of the puzzle to anticipate better individual BC risk and prognosis, pharmacokinetics, pharmacodynamics, and clinical efficacy. In recent years, it has been shown that gut microbiota may modulate cancer treatments' efficacy and adverse effects, and it is also apparent that both cancer itself and anticancer therapies interact with gut microbiota bidirectionally. Moreover, it has been proposed that certain gut microbes may protect the host against inappropriate inflammation and modulate the immune response. Future clinical research will determine if microbiota may be a prognostic and predictive factor of response to ICI and/or its side effects. Also, modulation of microbiota can be used to improve outcomes in BC patients. In this review, we discuss the potential implications of metabolomics and pharmacomicrobiomics that might impact BC immunotherapy treatment.
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spelling Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent DevelopmentsNeoplasias da MamaMicrobiotaBreast NeoplasmsBreast cancer (BC) is the most common malignancy and the second cause of cancer-specific death in women from high-income countries. Infectious agents are the third most important risk factor for cancer incidence after tobacco and obesity. Dysbiosis emerged as a key player that may influence cancer development, treatment, and prognosis through diverse biological processes. Metastatic BC has a highly variable clinical course, and more recently, immune checkpoint inhibitors (ICIs) have become an emerging therapy in BC. Even with standardised treatment protocols, patients do not respond similarly, reflecting each individual´s heterogeneity, unique BC features, and tumour microenvironment. However, there is insufficient data regarding predictive factors of response to available treatments for BC. The microbiota could be a crucial piece of the puzzle to anticipate better individual BC risk and prognosis, pharmacokinetics, pharmacodynamics, and clinical efficacy. In recent years, it has been shown that gut microbiota may modulate cancer treatments' efficacy and adverse effects, and it is also apparent that both cancer itself and anticancer therapies interact with gut microbiota bidirectionally. Moreover, it has been proposed that certain gut microbes may protect the host against inappropriate inflammation and modulate the immune response. Future clinical research will determine if microbiota may be a prognostic and predictive factor of response to ICI and/or its side effects. Also, modulation of microbiota can be used to improve outcomes in BC patients. In this review, we discuss the potential implications of metabolomics and pharmacomicrobiomics that might impact BC immunotherapy treatment.Repositório ComumVitorino, MBaptista de Almeida, SAlpuim Costa, DFaria, ACalhau, CAzambuja Braga, S2022-08-07T21:08:21Z20222022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.26/41551engFront Oncol . 2022 Jan 28;11:815772.10.3389/fonc.2021.815772info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-12-20T14:25:29Zoai:comum.rcaap.pt:10400.26/41551Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:23:00.035433Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
title Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
spellingShingle Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
Vitorino, M
Neoplasias da Mama
Microbiota
Breast Neoplasms
title_short Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
title_full Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
title_fullStr Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
title_full_unstemmed Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
title_sort Human Microbiota and Immunotherapy in Breast Cancer - A Review of Recent Developments
author Vitorino, M
author_facet Vitorino, M
Baptista de Almeida, S
Alpuim Costa, D
Faria, A
Calhau, C
Azambuja Braga, S
author_role author
author2 Baptista de Almeida, S
Alpuim Costa, D
Faria, A
Calhau, C
Azambuja Braga, S
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Comum
dc.contributor.author.fl_str_mv Vitorino, M
Baptista de Almeida, S
Alpuim Costa, D
Faria, A
Calhau, C
Azambuja Braga, S
dc.subject.por.fl_str_mv Neoplasias da Mama
Microbiota
Breast Neoplasms
topic Neoplasias da Mama
Microbiota
Breast Neoplasms
description Breast cancer (BC) is the most common malignancy and the second cause of cancer-specific death in women from high-income countries. Infectious agents are the third most important risk factor for cancer incidence after tobacco and obesity. Dysbiosis emerged as a key player that may influence cancer development, treatment, and prognosis through diverse biological processes. Metastatic BC has a highly variable clinical course, and more recently, immune checkpoint inhibitors (ICIs) have become an emerging therapy in BC. Even with standardised treatment protocols, patients do not respond similarly, reflecting each individual´s heterogeneity, unique BC features, and tumour microenvironment. However, there is insufficient data regarding predictive factors of response to available treatments for BC. The microbiota could be a crucial piece of the puzzle to anticipate better individual BC risk and prognosis, pharmacokinetics, pharmacodynamics, and clinical efficacy. In recent years, it has been shown that gut microbiota may modulate cancer treatments' efficacy and adverse effects, and it is also apparent that both cancer itself and anticancer therapies interact with gut microbiota bidirectionally. Moreover, it has been proposed that certain gut microbes may protect the host against inappropriate inflammation and modulate the immune response. Future clinical research will determine if microbiota may be a prognostic and predictive factor of response to ICI and/or its side effects. Also, modulation of microbiota can be used to improve outcomes in BC patients. In this review, we discuss the potential implications of metabolomics and pharmacomicrobiomics that might impact BC immunotherapy treatment.
publishDate 2022
dc.date.none.fl_str_mv 2022-08-07T21:08:21Z
2022
2022-01-01T00:00:00Z
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dc.relation.none.fl_str_mv Front Oncol . 2022 Jan 28;11:815772.
10.3389/fonc.2021.815772
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