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Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC
Triple-negative breast cancer (TNBC) presents significant challenges to female health owing to the lack of therapeutic targets and its poor prognosis. In recent years, in the field of molecular pathology, there has been a growing focus on the role of intra-tumoral microbial communities and metabolic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602718/ https://www.ncbi.nlm.nih.gov/pubmed/37901331 http://dx.doi.org/10.3389/fonc.2023.1143163 |
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author | Wang, Yi Qu, Dingding Zhang, Yali Jin, Yiping Feng, Yu Zhang, He Xia, Qingxin |
author_facet | Wang, Yi Qu, Dingding Zhang, Yali Jin, Yiping Feng, Yu Zhang, He Xia, Qingxin |
author_sort | Wang, Yi |
collection | PubMed |
description | Triple-negative breast cancer (TNBC) presents significant challenges to female health owing to the lack of therapeutic targets and its poor prognosis. In recent years, in the field of molecular pathology, there has been a growing focus on the role of intra-tumoral microbial communities and metabolic alterations in tumor cells. However, the precise mechanism through which microbiota and their metabolites influence TNBC remains unclear and warrants further investigation. In this study, we analyzed the microbial community composition in various subtypes of breast cancer through 16S rRNA MiSeq sequencing of formalin-fixed, paraffin-embedded (FFPE) tissue samples. Notably, Turicibacter, a microbe associated with cancer response, exhibited a significantly higher abundance in TNBC. Similarly, mass spectrometry-based metabolomic analysis revealed substantial differences in specific metabolites, such as nutriacholic, pregnanetriol, and cortol. Furthermore, we observed significant correlations between the intra-tumoral microbiome, clinicopathological characteristics, and human epidermal growth factor receptor-2 expression(HER2). Three microbial taxa (Cytophagaceae, Conexibacteraceae, and Flavobacteriaceae) were associated with tumor-infiltrating lymphocytes(TILs), which are indicative of antitumor immunity. This study creatively utilized FFPE tissue samples to assess intra-tumoral microbial communities and their related metabolic correlations, presenting avenues for the identification of novel diagnostic biomarkers, the development of therapeutic strategies, and the early clinical diagnosis of TNBC. |
format | Online Article Text |
id | pubmed-10602718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106027182023-10-27 Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC Wang, Yi Qu, Dingding Zhang, Yali Jin, Yiping Feng, Yu Zhang, He Xia, Qingxin Front Oncol Oncology Triple-negative breast cancer (TNBC) presents significant challenges to female health owing to the lack of therapeutic targets and its poor prognosis. In recent years, in the field of molecular pathology, there has been a growing focus on the role of intra-tumoral microbial communities and metabolic alterations in tumor cells. However, the precise mechanism through which microbiota and their metabolites influence TNBC remains unclear and warrants further investigation. In this study, we analyzed the microbial community composition in various subtypes of breast cancer through 16S rRNA MiSeq sequencing of formalin-fixed, paraffin-embedded (FFPE) tissue samples. Notably, Turicibacter, a microbe associated with cancer response, exhibited a significantly higher abundance in TNBC. Similarly, mass spectrometry-based metabolomic analysis revealed substantial differences in specific metabolites, such as nutriacholic, pregnanetriol, and cortol. Furthermore, we observed significant correlations between the intra-tumoral microbiome, clinicopathological characteristics, and human epidermal growth factor receptor-2 expression(HER2). Three microbial taxa (Cytophagaceae, Conexibacteraceae, and Flavobacteriaceae) were associated with tumor-infiltrating lymphocytes(TILs), which are indicative of antitumor immunity. This study creatively utilized FFPE tissue samples to assess intra-tumoral microbial communities and their related metabolic correlations, presenting avenues for the identification of novel diagnostic biomarkers, the development of therapeutic strategies, and the early clinical diagnosis of TNBC. Frontiers Media S.A. 2023-10-12 /pmc/articles/PMC10602718/ /pubmed/37901331 http://dx.doi.org/10.3389/fonc.2023.1143163 Text en Copyright © 2023 Wang, Qu, Zhang, Jin, Feng, Zhang and Xia https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Wang, Yi Qu, Dingding Zhang, Yali Jin, Yiping Feng, Yu Zhang, He Xia, Qingxin Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title | Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title_full | Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title_fullStr | Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title_full_unstemmed | Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title_short | Intra-tumoral microbial community profiling and associated metabolites alterations of TNBC |
title_sort | intra-tumoral microbial community profiling and associated metabolites alterations of tnbc |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602718/ https://www.ncbi.nlm.nih.gov/pubmed/37901331 http://dx.doi.org/10.3389/fonc.2023.1143163 |
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