From: Progress of mesenchymal stem cell-derived exosomes in targeted delivery of antitumor drugs
Drug | Source of exosomes | In vivo model | Tumor type | Loading method | Therapeutic effect | Reference |
---|---|---|---|---|---|---|
miR-145-5p | Human Umbilical cord | PDAC mice | Pancreatic | Transfection | Increased tumor cell apoptosis and significantly inhibited tumor growth | [110] |
miR-381 | Bone marrow | None | Breast cancer | Electroporation | migratory and invasive capacity and promotes apoptosis | [111] |
miR-499 | Bone marrow | BALB/c nude mice | Endometrial cancer | Electroporation | Significantly inhibited endometrial cancer cell proliferation, endothelial cell tube formation, and inhibited tumor growth and angiogenesis | [112] |
LNA anti-miR-142-3p | Bone marrow | SCID mice | Breast cancer | Electroporation | Reduced tumorigenicity of breast cancer stem cells in vivo | [113] |
miR-124 | Bone marrow | BALB/c nude mice | Pancreatic | Transfection | Inhibited cell proliferation, metastasis and epithelial mesenchymal transition and enhanced chemosensitivity to 5-fluorouracil in vitro and in vivo | [114] |
Tumor Necrosis Factor α | Bone marrow | BALB/c nude mice | Melanoma | Electroporation | Good targeting properties, better anti-tumor activity and lower toxicity | [115] |