Bacillus mojavensis postbiotics: transcriptomic and anticancer effects in colon cancer cells.
[UNLABELLED] Probiotics have been shown to exert antiproliferative effects on colon cancer cells.
APA
Trujillo-López MA, Muñoz-Olivos C, et al. (2026). Bacillus mojavensis postbiotics: transcriptomic and anticancer effects in colon cancer cells.. AMB Express, 16(1). https://doi.org/10.1186/s13568-026-02018-4
MLA
Trujillo-López MA, et al.. "Bacillus mojavensis postbiotics: transcriptomic and anticancer effects in colon cancer cells.." AMB Express, vol. 16, no. 1, 2026.
PMID
41779268
Abstract
[UNLABELLED] Probiotics have been shown to exert antiproliferative effects on colon cancer cells. While these effects are often attributed to microbiome regulation, they may also result from bioactive metabolites produced by probiotic bacteria. In the present study, we investigated the impact of a cell-free extract, hereafter referred to as a postbiotic, derived from , a strain isolated from (a traditional Mexican beverage). The antiproliferative activity was evaluated in SW480 human colon cancer cells using MTT and crystal violet assays, while antimigratory effects were assessed through a wound-healing assay. In addition, the ability of the postbiotic to counteract inflammatory proliferation was evaluated in SW480 cells treated with lipopolysaccharide (LPS). Biosafety was tested using peripheral blood mononuclear cells (PBMCs) from healthy donors. Results demonstrated that treatment with 25–50 µg/mL of postbiotic reduced SW480 cell viability by 75.15% and 79.3%, respectively, and significantly inhibited cell migration after 24 h. Moreover, the postbiotic decreased LPS-induced proliferation without exerting any cytotoxic effect on PBMCs, underscoring its selectivity toward malignant cells. To elucidate the underlying mechanisms, transcriptomic profiling was performed, revealing extensive modulation of oncogenes and tumor suppressors, with enrichment of PI3K–Akt, MAPK, apoptosis, and cytokine receptor pathways. In conclusion, postbiotics from isolated from exhibit selective anticancer activity by inhibiting proliferation, migration, and inflammation-induced growth in colorectal cancer cells. Transcriptomic findings further support these effects.
[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s13568-026-02018-4.
[SUPPLEMENTARY INFORMATION] The online version contains supplementary material available at 10.1186/s13568-026-02018-4.