MiR26a reverses enzalutamide resistance in a bone-tumor targeted system with an enhanced effect on bone metastatic CRPC
Wang, Yuanyuan; Chen, Jiyuan; Gong, Luyao; Wang, Yunxia; Siltari, Aino; Lou, Yan Ru; Murtola, Teemu J.; Gao, Shen; Gao, Yuan (2024-04)
Wang, Yuanyuan
Chen, Jiyuan
Gong, Luyao
Wang, Yunxia
Siltari, Aino
Lou, Yan Ru
Murtola, Teemu J.
Gao, Shen
Gao, Yuan
04 / 2024
Journal of Nanobiotechnology
145
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202404163611
https://urn.fi/URN:NBN:fi:tuni-202404163611
Kuvaus
Peer reviewed
Tiivistelmä
<p>Resistance to androgen receptor (AR) inhibitors, including enzalutamide (Enz), as well as bone metastasis, are major challenges for castration-resistant prostate cancer (CRPC) treatment. In this study, we identified that miR26a can restore Enz sensitivity and inhibit bone metastatic CRPC. To achieve the highest combination effect of miR26a and Enz, we developed a cancer-targeted nano-system (Bm@PT/Enz-miR26a) using bone marrow mesenchymal stem cell (BMSC) membrane and T140 peptide to co-deliver Enz and miR26a. The in vitro/in vivo results demonstrated that miR26a can reverse Enz resistance and synergistically shrink tumor growth, invasion, and metastasis (especially secondary metastasis) in both subcutaneous and bone metastatic CRPC mouse models. We also found that the EZH2/SFRP1/WNT5A axis may be involved in this role. These findings open new avenues for treating bone metastatic and Enz-resistant CRPC.</p>
Kokoelmat
- TUNICRIS-julkaisut [20724]