Evidence map›Paper›PMID 40898175›Full record

ArticleBMC complementary medicine and therapies2025

The potential of probiotic derivatives of Bacillus coagulans Hammer on induction of apoptosis in colorectal adenocarcinoma cell line in vitro.

Maryam Mashhoori Vayghan, Parvaneh Saffarian, Maryam Tajabadi Ebrahimi, Hamid Asadzadeh Aghdaei, Abbas Yadegar

Abstract read
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Article in BMC complementary medicine and therapies, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Maryam Mashhoori VayghanDepartment of Biology, SR.C., Islamic Azad University, Tehran, Iran.
Parvaneh SaffarianDepartment of Biology, SR.C., Islamic Azad University, Tehran, Iran.
Maryam Tajabadi EbrahimiDepartment of Biology, CT.C, Islamic Azad University, Tehran, Iran.
Hamid Asadzadeh AghdaeiBasic and Molecular Epidemiology of Gastrointestinal Disorders Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abbas YadegarFoodborne and Waterborne Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran. a.yadegar@sbmu.ac.ir.ORCID http://orcid.org/0000-0002-2135-7581

Funding

Shahid Beheshti University of Medical Sciences RIGLD 1140
6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) remains as one of the leading causes of human morbidity and mortality worldwide. Dysbiosis in the structure of the gut microbiota resulting in increased abundance of harmful bacteria and decreased beneficial bacteria has been frequently associated with CRC development. Recently, probiotics and their derivatives have received great attention as anticancer agents for prevention and treatment of various cancers. This study aimed to assess the potential effects of probiotic Bacillus coagulans Hammer and its derivatives on induction of apoptosis in human colon adenocarcinoma cell lines in vitro.

methodsCell viability of HT-29 and Caco-2 cells was examined by MTT assay after exposure to varying concentrations of pasteurized and UV-killed B. coagulans Hammer, its extracellular vesicles (EVs), and cell-free supernatant (CFS). The apoptotic effects of different B. coagulans Hammer derivatives on HT-29 and Caco-2 cells were determined by analyzing the expression level of apoptosis-related genes (Bad, Bax, Bcl-2, Caspase-3, Caspase-9) using RT-qPCR assay. Annexin V-FITC/PI flow cytometry was performed to assess apoptosis. Protein expression of Bax and Bcl-2 was measured by Western blotting.

resultsHigh concentrations of B. coagulans Hammer derivatives significantly (P < 0.05) reduced viability of HT-29 and Caco-2 cells compared to untreated control. The results of RT-qPCR assay showed significant decrease in the expression level of antiapoptotic gene Bcl-2, and notable increase in the expression level of proapoptotic genes Bax, Bad, Caspase-3, and Caspase-9 in HT-29 and Caco-2 cells by B. coagulans Hammer derivatives. Flow cytometry demonstrated a high percentage of apoptotic HT-29 cells compared to untreated cells after exposure to B. coagulans Hammer derivatives. Western blotting analysis confirmed that treatment with EVs, UV-killed cells, and CFS significantly decreased Bcl-2 expression, and increased Bax expression in HT-29 cells.

conclusionsOur findings suggest that derivatives of probiotic B. coagulans Hammer can exert anticancer activity by induction of apoptosis in colon cancer HT-29 and Caco-2 cells. Further investigations are required to validate the safety and efficacy of B. coagulans Hammer derivatives in CRC prevention and treatment.

Indexed as

AdenocarcinomaApoptosisBacillus coagulansColorectal NeoplasmsProbioticsCaco-2 CellsCell SurvivalHT29 CellsHumansApoptosisBacillus coagulans hammerColon cancer cellsExtracellular vesiclesFlow cytometryProbiotics

Identifiers

PMID40898175
PMCPMC12403276

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