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MiR26a 在骨肿瘤靶向系统中逆转恩杂鲁胺耐药并增强对骨转移性 CRPC 的效应

英文原题:MiR26a reverses enzalutamide resistance in a bone-tumor targeted system with an enhanced effect on bone metastatic CRPC.

PubMed 2024/04/02(内容时间) J Nanobiotechnology Q1 · IF 15(JCR 2025)

研究概要

对雄激素受体(AR)抑制剂(包括恩杂鲁胺(Enz))的耐药以及骨转移,是去势抵抗性前列腺癌(CRPC)治疗面临的主要挑战。

中文摘要

对雄激素受体(AR)抑制剂(包括enzalutamide,Enz)的耐药以及骨转移,是去势抵抗性前列腺癌(CRPC)治疗的主要挑战。本研究发现,miR26a可恢复对Enz的敏感性,并抑制骨转移性CRPC。为最大化miR26a与Enz的联合效果,我们利用骨髓间充质干细胞(BMSC)膜和T140肽开发了肿瘤靶向纳米系统Bm@PT/Enz-miR26a,共递送Enz和miR26a。体内外结果表明,miR26a可逆转Enz耐药,并在皮下和骨转移CRPC小鼠模型中协同抑制肿瘤生长、侵袭和转移(尤其是继发转移)。我们还发现EZH2/SFRP1/WNT5A轴可能参与这一作用。这些发现为治疗骨转移和Enz耐药CRPC开辟了新途径。

展开英文摘要原文

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.

论文信息

作者
Wang Y、Chen J、Gong L、Wang Y、Siltari A、Lou YR、Murtola TJ、Gao S
第一作者单位
School of Pharmacy, Fudan University, Shanghai, 201206, China.China
通讯作者单位
School of Pharmacy, Fudan University, Shanghai, 201206, China. yuan_gao@fudan.edu.cn.China
期刊
Journal of nanobiotechnology2024 Apr 2
原文标识
PubMed 38566211 · DOI 10.1186/s12951-024-02438-z