Based on transcriptional predictions, the MSC1 cells were proposed to upregulate canonical tumor-suppressive ligands, including TRAIL, TL1A, LIGHT, and BMPs, which drive apoptosis and growth arrest in colorectal and other cancers [31,32,33,34,35,36,37,38,39,40,41]. This evidence concerns the gene TNFSF10 and neoplasm.