Affiliation:
1. Istanbul University
2. Istanbul University Istanbul Faculty of Medicine: Istanbul Universitesi Istanbul Tip Fakultesi
3. İstanbul Bakırköy Dr Sadi Konuk Egitim ve Arastirma Hastanesi: Istanbul Bakirkoy Dr Sadi Konuk Egitim ve Arastirma Hastanesi
4. Istanbul University School of Medicine: Istanbul Universitesi Istanbul Tip Fakultesi
Abstract
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. HCT-116 and HT-29 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 ficoll-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 flow 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 significantly higher in 72-hour incubations (p<0.006), whereas the effect of cord blood mesenchymal stem cell in 24-hour 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.
Publisher
Research Square Platform LLC