Mesenchymal stem cells desensitize castration-resistant prostate cancer to docetaxel chemotherapy via inducing TGF-[beta]1-mediated cell autophagy

• Published in: Cell & bioscience Vol. 11; no. 1
• Main Authors: Yu, Yang, Yang, Fu-han, Zhang, Wen-tao, Guo, Ya-dong, Ye, Lin, Yao, Xu-dong
• Format: Journal Article
• Language: English
• Published: BioMed Central Ltd 07.01.2021
• Subjects: Antimitotic agents; Antineoplastic agents; Apoptosis; Bone morphogenetic proteins; Cancer; Chemotherapy; Cholecystokinin; Enzyme-linked immunosorbent assay; Enzymes; Prostate cancer; RNA; Stem cells; Transforming growth factors
• ISSN: 2045-3701; 2045-3701
• DOI: 10.1186/s13578-020-00494-0

Mesenchymal stem cells (MSCs) have been proved to drive castration resistant prostate cancer (CRPC). In this study, we aim to investigate the contribution of MSCs to the development of docetaxel resistance in CRPC cells and its potential mechanisms. The effect of MSCs on CRPC cells resistance to docetaxel was determined using in vivo and in vitro approaches. CCK8 and PI/Annexin V-FITC assay were used to examined the cell viability and apoptosis. The concentration of transforming growth factor-[beta]1 was measured by enzyme-linked immunosorbent assay and small interfering RNA was used for functional analyses. MSCs significantly reduced the sensitivity of CRPC cells to docetaxel-induced proliferation inhibition and apoptosis promotion in vivo and in vitro. CRPC cells cocultured with MSCs under docetaxel administration have an increased autophagy activation, while autophagy inhibitor could effectively reversed MSCs-induced resistance to docetaxel. Additionally, MSCs-induced CRPC cell autophagy increase under docetaxel administration depends on MSCs secreting TGF-[beta]1 and inhibition of TGF-[beta]1 secretion in MSCs could consequently increase the sensitivity of CRPC cells to docetaxel. These results suggest that docetaxel administrated CRPC cells may elicit MSCs secreting TGF-[beta]1 increase, which desensitizes CRPC to docetaxel chemotherapy accelerating chemoresistance occurrence via inducing cell autophagy.