AD-MSC-EXOs |
Bladder cancer |
miR-138-5p |
Tumor suppressor |
Subcutaneous injections |
This method is an efficient delivery carrier for small molecule medications in vivo, and EXOs-carried miR-138-5p is a hopeful curative factor for BC therapy |
[166] |
BM-MSC-EXOs |
Liver cancer |
miR-205–5p |
Tumor suppressor |
Subcutaneously injected |
This technique has inhibitory efficacy on the development of liver cancer via controlling CDKL3 |
[121] |
hUC-MSC-EXOs |
Hepatoma |
miR-451a |
Tumor suppressor |
– |
HUC-MSC-EXOs miR-451a suppressed ADAM10 to inhibit the chemotherapy resistance, cell cycle transition, proliferation, cancer cell development, and progression, and increase apoptosis of Hepatoma cells |
[167] |
hUC-MSC-EXOs |
Wilms tumor |
miR-15a-5p |
Tumor suppressor |
Subcutaneously injected |
This miRNA delivered via hUC-MSCs-Exo downregulates SEPT2 expression and inhibits WT cell development in vivo and in vitro |
[168] |
AD-MSC-EXOs |
Triple-negative breast cancer (TNBC) |
miR-381-3p |
Tumor suppressor |
– |
EXOs-miR-381 suppressed the growth, migration, and invasion malignancy of breast cancer cells and increased their apoptosis in vitro |
[122] |
BM-MSC-EXOs |
Acute myeloid leukemia (AML) |
miR-7-5p |
Tumor suppressor |
Injected via a tail vein |
Exo-miR-7-5p downregulates OSBPL11 via inhibiting the phosphorylation of the PI3K/AKT/mTOR signaling pathway, thus suppressing AML growth and increasing apoptosis |
[123] |
BM-MSC-EXOs |
Breast cancer |
LNA-anti-miR-142 |
OncomiRs |
Intravenous injection |
BM-MSC-EXOs can successfully transport anti-miR-142-3p to decrease the miR-142-3p and miR-150 rates and enhance the transcription of the regulative target genes (APC and P2X7R) |
[169] |
DP-MSC-EXOs |
Breast carcinoma cells |
miR-34a |
Tumor suppressor |
– |
Genetically altered DP-MSCs were able to discharge of EXOs enriched with curative miRNAs and offered the possibility of use of EXO-based carrier for gene distribution |
[170] |
BM-MSC-EXOs |
Castration-resistant prostate cancer (CRPC) |
miR-let-7c |
Tumor suppressor |
– |
These miRNAs can be effectively loaded into BM-MSC-EXOs. Therapy without carrier or MSC-EXOs-entrapped miR-let-7c led to remarkable decreases in cell proliferation and development in CRPC cells |
[124] |
BM-MSC-EXOs |
Glioma |
miR-146b |
Tumor suppressor |
Intratumoral injection |
Administration of an intratumoral dose of 50 μg miR-146 loaded in BM-MSC-EXOs remarkably decreased glioma xenograft development in rat brains |
[125] |
BM-MSC-EXOs |
Glioblastoma Multiforme |
miR-9 |
OncomiRs |
– |
To inhibit miR-9, techniques were created with Cy5-tagged anti-miR-9. This method leads to enhanced apoptosis and caspase action |
[171] |