The expression of OSBPL10 in platinum-resistant HRD-positive ovarian cancer patients were significantly higher than that in platinum-sensitive patients. Inhibiting OSBPL10 enhanced the sensitivity to cisplatin and Niraparib of ovarian cancer cells. Apolipoprotein E (APOE), as a target gene of OSBPL10, was involved in lipid transport and lipoprotein metabolism.
Exo-miR-7-5p derived from BMSCs negatively regulates OSBPL11 by suppressing the phosphorylation of the PI3K/AKT/mTOR signaling pathway, thereby inhibiting AML proliferation and promoting apoptosis. The data will inform the development of AML therapies based on BMSC-derived exosomes.