Suppression of viability and migration in a human colorectal cancer cell line, HT-29, by 7SK long non-coding RNA

Background and Aim: 7SK is a long non-coding RNA that interacts with various proteins to regulate gene transcription. This study aimed to assess the impact of exosomal delivery of 7SK on viability, expression of apoptosis-related genes, and migration in the human colorectal cancer cell line HT-29. Methods: In this experimental study, HT-29 cells were treated with exosomes derived from human umbilical cord mesenchymal stem cells loaded with 7SK (Exo-7SK). Control groups included cells treated with unloaded exosomes and untreated cells. The levels of 7SK in the cells, and expression of apoptosis-related genes were measured by real-time PCR, cell viability assessed by the MTT assay, and cell migration evaluated using the transwell assay. Results: Treatment of HT-29 cells with Exo-7SK resulted in increased levels of 7SK, reduced viability, downregulation of the anti-apoptotic gene BCL-2, upregulation of the apoptosis-inducing gene BAX, and decreased migration. Conclusion: Exosomal delivery of 7SK can effectively decrease the viability and migration of colorectal cancer cells. Further research is warranted to explore the therapeutic potential of this approach in colorectal cancer.