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. 2021 May;24(5):561–576. doi: 10.22038/ijbms.2021.54735.12277

Table 5.

Application of genetically modified MSCs in other GI cancer therapy

Cancer Transfected gene Source of MSCs Vector Anti-cancer effects ref
OC TRAIL Human
BMSCs
Lentivirus Increased cancer cell apoptosis in vitro and significantly reduce tumor growth and metastasis in vivo. (137)
OC IFN-β Human
GMSCs
Lentivirus Inhibited proliferation of TSCC cells and increased apoptosis. Decreased tumor volume and lowered number of cancer cells in vivo. (139)
OC TRAIL Human
GMSCs
Lentivirus In vitro: increased cell death and apoptosis. In vivo: reduced and inhibited TSCC growth. (138)
ESCC miR-375 Human UCMSCs Plasmid Suppressed ESCC cell proliferation, invasion, migration, tumorsphere formation, and increased apoptosis in vitro, furthermore decreased tumor growth in vivo. (141)
ESCC TRAIL Human
BMSCs
Adenovirus Inhibited proliferation and induced apoptosis in vitro also repressed tumor growth in vivo (140)
GC  CD Human
BMSCs
Plasmid Anticancer activity in cell line and decreased tumor volume in a mouse model (142)
GC TNF-α Human UCMSCs Lentivirus Inhibited gastric cancers growth in vivo (143)
GC LIGHT (TNFSF14) Human UCMSCs Lentivirus Inhibited tumor growth and increased necrosis in vivo. (146)
GC NK4 Human
BMSCs
Lentivirus Migration ability and anti-cancer activity in cell line and gastric cancer xenografts model. (147)

OC: Oral cancer; ESCC: Esophageal squamous cell carcinoma; GC: Gastric cancer; BMSCs: Bone marrow-derived MSCs; UCMSCs: Umbilical cord-derived MSCs; GMSCs: Gingival-derived MSCs; MSCs: Mesenchymal stem cells; GI cancer: Gastrointestinal cancers