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Mechanistic Insights into the Anti-Proliferative Action of Gut Microbial Metabolites against Breast Adenocarcinoma Cells
被引:5
|作者:
Jaye, Kayla
[1
]
Alsherbiny, Muhammad A.
[1
,2
,3
]
Chang, Dennis
[1
]
Li, Chun-Guang
[1
]
Bhuyan, Deep Jyoti
[1
,4
]
机构:
[1] Western Sydney Univ, NICM Hlth Res Inst, Penrith, NSW 2751, Australia
[2] Cairo Univ, Fac Pharm, Pharmacognosy Dept, Cairo 11562, Egypt
[3] Victor Chang Cardiac Res Inst, Innovat Ctr, Sydney, NSW 2010, Australia
[4] Western Sydney Univ, Sch Sci, Penrith, NSW 2751, Australia
关键词:
gut microbial metabolites;
postbiotics;
breast cancer;
gut microbiome;
sodium butyrate;
inosine;
nisin;
NON-HDM2-MEDIATED PEPTIDE INHIBITOR;
BUTYRATE-INDUCED APOPTOSIS;
SODIUM-BUTYRATE;
P53;
UBIQUITINATION;
ESTROGEN-RECEPTOR;
CANCER CELLS;
PROLIFERATION;
PROTEIN;
LINES;
DIFFERENTIATION;
D O I:
10.3390/ijms242015053
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 IC50 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.
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