Lactobacillus casei condition medium downregulates miR-21 relative expression in HT-29 colorectal cancer cell line

Previous research has demonstrated promising outcomes regarding the advantageous impact of probiotics in both cancer prevention and treatment. Nevertheless, the precise molecular mechanisms underpinning these effects remain elusive. Recent investigations have proposed a potential involvement of micro ribonucleic acids (miRNAs) in mediating the favorable influence of probiotics on cancerous cells. This study was designed to evaluate the effect of Lactobacillus casei condition medium on miR-21 relative expression in HT-29 colorectal cancer cells. Lactobacillus casei condition medium mixed with RPMI in different proportions (1:1, 1:3, and 1:7) and utilized to treat HT-29 cells for 24 and 48 h. Subsequently, percentage of early and late apoptotic cells were identified using a flow cytometry instrument. A real-time polymerase chain reaction was carried out to determine the relative expression of miR-21. Our findings revealed that L. casei condition medium induces apoptosis in a time- and dose-dependent manner in HT-29 cells. Furthermore, we found a significantly downregulated miR-21 after treatment with high doses of L. casei condition medium after 48 h. Overall, our results provide valuable insights into a potential mechanism through which L. casei condition medium mediates its apoptotic effect in colorectal cancer cells through downregulation of miR-21. However, further investigations are required to unravel its therapeutic, diagnostic, and treatment monitoring potential. Lactobacillus casei condition medium downregulates miR-21 relative expression in HT-29 colorectal cancer cell line, which can potentially be related to induction of apoptosis in cancerous cells rather than in healthy cells.

Automated summary

This study investigated the effect of Lactobacillus casei condition medium on miR-21 expression in colorectal cancer cells. The results showed that L. casei condition medium induced apoptosis in HT-29 cells and significantly downregulated miR-21 expression after treatment with high doses of the medium.