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Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy

Microorganisms, including bacteria, viruses, fungi, and other eukaryotes, play critical roles in human health. An altered microbiome can be associated with complex diseases. Intratumoral microbial components are found in multiple tumor tissues and are closely correlated with cancer initiation and de...

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Autores principales: Yang, Li, Li, Aitian, Wang, Ying, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842669/
https://www.ncbi.nlm.nih.gov/pubmed/36646684
http://dx.doi.org/10.1038/s41392-022-01304-4
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author Yang, Li
Li, Aitian
Wang, Ying
Zhang, Yi
author_facet Yang, Li
Li, Aitian
Wang, Ying
Zhang, Yi
author_sort Yang, Li
collection PubMed
description Microorganisms, including bacteria, viruses, fungi, and other eukaryotes, play critical roles in human health. An altered microbiome can be associated with complex diseases. Intratumoral microbial components are found in multiple tumor tissues and are closely correlated with cancer initiation and development and therapy efficacy. The intratumoral microbiota may contribute to promotion of the initiation and progression of cancers by DNA mutations, activating carcinogenic pathways, promoting chronic inflammation, complement system, and initiating metastasis. Moreover, the intratumoral microbiota may not only enhance antitumor immunity via mechanisms including STING signaling activation, T and NK cell activation, TLS production, and intratumoral microbiota-derived antigen presenting, but also decrease antitumor immune responses and promote cancer progression through pathways including upregulation of ROS, promoting an anti-inflammatory environment, T cell inactivation, and immunosuppression. The effect of intratumoral microbiota on antitumor immunity is dependent on microbiota composition, crosstalk between microbiota and the cancer, and status of cancers. The intratumoral microbiota may regulate cancer cell physiology and the immune response by different signaling pathways, including ROS, β-catenin, TLR, ERK, NF-κB, and STING, among others. These viewpoints may help identify the microbiota as diagnosis or prognosis evaluation of cancers, and as new therapeutic strategy and potential therapeutic targets for cancer therapy.
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spelling pubmed-98426692023-01-18 Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy Yang, Li Li, Aitian Wang, Ying Zhang, Yi Signal Transduct Target Ther Review Article Microorganisms, including bacteria, viruses, fungi, and other eukaryotes, play critical roles in human health. An altered microbiome can be associated with complex diseases. Intratumoral microbial components are found in multiple tumor tissues and are closely correlated with cancer initiation and development and therapy efficacy. The intratumoral microbiota may contribute to promotion of the initiation and progression of cancers by DNA mutations, activating carcinogenic pathways, promoting chronic inflammation, complement system, and initiating metastasis. Moreover, the intratumoral microbiota may not only enhance antitumor immunity via mechanisms including STING signaling activation, T and NK cell activation, TLS production, and intratumoral microbiota-derived antigen presenting, but also decrease antitumor immune responses and promote cancer progression through pathways including upregulation of ROS, promoting an anti-inflammatory environment, T cell inactivation, and immunosuppression. The effect of intratumoral microbiota on antitumor immunity is dependent on microbiota composition, crosstalk between microbiota and the cancer, and status of cancers. The intratumoral microbiota may regulate cancer cell physiology and the immune response by different signaling pathways, including ROS, β-catenin, TLR, ERK, NF-κB, and STING, among others. These viewpoints may help identify the microbiota as diagnosis or prognosis evaluation of cancers, and as new therapeutic strategy and potential therapeutic targets for cancer therapy. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842669/ /pubmed/36646684 http://dx.doi.org/10.1038/s41392-022-01304-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Yang, Li
Li, Aitian
Wang, Ying
Zhang, Yi
Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title_full Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title_fullStr Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title_full_unstemmed Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title_short Intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
title_sort intratumoral microbiota: roles in cancer initiation, development and therapeutic efficacy
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842669/
https://www.ncbi.nlm.nih.gov/pubmed/36646684
http://dx.doi.org/10.1038/s41392-022-01304-4
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