The in vitro treatment of mesenchymal stem cells for colorectal cancer cells

Abstract

Colorectal cancer is the most common tumor of the gastrointestinal system. The conventional treatment options of colorectal cancer are troublesome for both patients and clinicians. Recently, mesenchymal stem cells (MSCs) have been the novel focus for cell therapy due to its migration to tumor sites. In this study, the apoptotic effect of MSCs on colorectal cancer cell lines has been aimed. were selected as the colorectal cancer cell lines. Human umbilical cord blood and Wharton's jelly were used as mesenchymal stem cell sources. To discriminate against the apoptotic effect of MSC on cancer, we also used peripheral blood mononuclear cells (PBMC) as a healthy control group. Cord blood-MSC and PBMC were obtained by coll-paque density gradient, and Wharton's jelly-MSC by explant method.Transwell co-culture systems were used as cancer cells or PBMC/MSCs at ratios of 1/5 and 1/10, incubation times of 24 hours and 72 hours. The Annexin V/PI-FITC based apoptosis assay was performed by ow cytometry. Caspase-3 and HTRA2/Omi proteins were measured by ELISA. For both ratios in both cancer cells, it was found that the apoptotic effect of Wharton's jelly-MSC was signi cantly higher in 72-hour incubations (p<0.006), whereas the effect of cord blood mesenchymal stem cell in 24hour incubations were higher (p<0.007). In this study, we showed that human cord blood and tissue derived MSCs treatment led colorectal cancers to apoptosis. We anticipate that further in vivo studies may shed light on the apoptotic effect of MSC. *For PBMC and MSCs treatment comparison, Wilcoxon test were used. The signi cance value was determined as p<0.05.Table 2 The comparison of HTRA2/Omi related to change of MSC sources