Cargando…

Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells

The gut microbiota undergoes metabolic processes to produce by-products (gut metabolites), which play a vital role in the overall maintenance of health and prevention of disease within the body. However, the use of gut metabolites as anticancer agents and their molecular mechanisms of action are lar...

Descripción completa

Detalles Bibliográficos
Autores principales: Jaye, Kayla, Alsherbiny, Muhammad A., Chang, Dennis, Li, Chun-Guang, Bhuyan, Deep Jyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606851/
https://www.ncbi.nlm.nih.gov/pubmed/37894734
http://dx.doi.org/10.3390/ijms242015053
_version_ 1785127413713207296
author Jaye, Kayla
Alsherbiny, Muhammad A.
Chang, Dennis
Li, Chun-Guang
Bhuyan, Deep Jyoti
author_facet Jaye, Kayla
Alsherbiny, Muhammad A.
Chang, Dennis
Li, Chun-Guang
Bhuyan, Deep Jyoti
author_sort Jaye, Kayla
collection PubMed
description The gut microbiota undergoes metabolic processes to produce by-products (gut metabolites), which play a vital role in the overall maintenance of health and prevention of disease within the body. However, the use of gut metabolites as anticancer agents and their molecular mechanisms of action are largely unknown. Therefore, this study evaluated the anti-proliferative effects of three key gut microbial metabolites—sodium butyrate, inosine, and nisin, against MCF7 and MDA-MB-231 breast adenocarcinoma cell lines. To determine the potential mechanistic action of these gut metabolites, flow cytometric assessments of apoptotic potential, reactive oxygen species (ROS) production measurements and proteomics analyses were performed. Sodium butyrate exhibited promising cytotoxicity, with IC(50) values of 5.23 mM and 5.06 mM against MCF7 and MDA-MB-231 cells, respectively. All three metabolites were found to induce apoptotic cell death and inhibit the production of ROS in both cell lines. Nisin and inosine indicated a potential activation of cell cycle processes. Sodium butyrate indicated the possible initiation of signal transduction processes and cellular responses to stimuli. Further investigations are necessary to ascertain the effective therapeutic dose of these metabolites, and future research on patient-derived tumour spheroids will provide insights into the potential use of these gut metabolites in cancer therapy.
format Online
Article
Text
id pubmed-10606851
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-106068512023-10-28 Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells Jaye, Kayla Alsherbiny, Muhammad A. Chang, Dennis Li, Chun-Guang Bhuyan, Deep Jyoti Int J Mol Sci Article The gut microbiota undergoes metabolic processes to produce by-products (gut metabolites), which play a vital role in the overall maintenance of health and prevention of disease within the body. However, the use of gut metabolites as anticancer agents and their molecular mechanisms of action are largely unknown. Therefore, this study evaluated the anti-proliferative effects of three key gut microbial metabolites—sodium butyrate, inosine, and nisin, against MCF7 and MDA-MB-231 breast adenocarcinoma cell lines. To determine the potential mechanistic action of these gut metabolites, flow cytometric assessments of apoptotic potential, reactive oxygen species (ROS) production measurements and proteomics analyses were performed. Sodium butyrate exhibited promising cytotoxicity, with IC(50) values of 5.23 mM and 5.06 mM against MCF7 and MDA-MB-231 cells, respectively. All three metabolites were found to induce apoptotic cell death and inhibit the production of ROS in both cell lines. Nisin and inosine indicated a potential activation of cell cycle processes. Sodium butyrate indicated the possible initiation of signal transduction processes and cellular responses to stimuli. Further investigations are necessary to ascertain the effective therapeutic dose of these metabolites, and future research on patient-derived tumour spheroids will provide insights into the potential use of these gut metabolites in cancer therapy. MDPI 2023-10-10 /pmc/articles/PMC10606851/ /pubmed/37894734 http://dx.doi.org/10.3390/ijms242015053 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jaye, Kayla
Alsherbiny, Muhammad A.
Chang, Dennis
Li, Chun-Guang
Bhuyan, Deep Jyoti
Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title_full Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title_fullStr Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title_full_unstemmed Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title_short Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
title_sort mechanistic insights into the anti-proliferative action of gut microbial metabolites against breast adenocarcinoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10606851/
https://www.ncbi.nlm.nih.gov/pubmed/37894734
http://dx.doi.org/10.3390/ijms242015053
work_keys_str_mv AT jayekayla mechanisticinsightsintotheantiproliferativeactionofgutmicrobialmetabolitesagainstbreastadenocarcinomacells
AT alsherbinymuhammada mechanisticinsightsintotheantiproliferativeactionofgutmicrobialmetabolitesagainstbreastadenocarcinomacells
AT changdennis mechanisticinsightsintotheantiproliferativeactionofgutmicrobialmetabolitesagainstbreastadenocarcinomacells
AT lichunguang mechanisticinsightsintotheantiproliferativeactionofgutmicrobialmetabolitesagainstbreastadenocarcinomacells
AT bhuyandeepjyoti mechanisticinsightsintotheantiproliferativeactionofgutmicrobialmetabolitesagainstbreastadenocarcinomacells