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载 cRGD 靶向肝素纳米粒的双重载药系统用于顺铂耐药卵巢癌细胞的有效治疗

cRGD-targeted heparin nanoparticles for effective dual drug treatment of cisplatin-resistant ovarian cancer.

机构信息

Department of Obstetrics & Gynecology, Zhujiang Hospital; Cancer Research Institute, School of Basic Medical Sciences; Guangdong Provincial Key Laboratory of Immune Regulation and Immunotherapy, Southern Medical University, Guangzhou, Cuangdong, 510515, China.

Department of Obstetrics & Gynecology, Zhujiang Hospital; Cancer Research Institute, School of Basic Medical Sciences; Guangdong Provincial Key Laboratory of Immune Regulation and Immunotherapy, Southern Medical University, Guangzhou, Cuangdong, 510515, China.

出版信息

J Control Release. 2023 Apr;356:691-701. doi: 10.1016/j.jconrel.2023.03.017. Epub 2023 Mar 23.

Abstract

Resistance to the chemotherapeutic agent cisplatin (DDP) is the primary reason for invalid chemotherapy of ovarian cancer. Given the complex mechanisms underlying chemo-resistance, the design of combination therapies based on blocking multiple mechanisms is a rationale to synergistically elevate therapeutic effect for effectively overcoming cancer chemo-resistance. Herein, we demonstrated a multifunctional nanoparticle (DDP-Ola@HR), which could simultaneously co-deliver DDP and Olaparib (Ola, DNA damage repair inhibitor) using targeted ligand cRGD peptide modified with heparin (HR) as nanocarrier, enabling the concurrent tackling of multiple resistance mechanisms to effectively inhibit the growth and metastasis of DDP-resistant ovarian cancer. In combination strategy, heparin could suppress the function of multidrug resistance-associated protein 2 (MRP2) and P-glycoprotein (P-gp) to promote the intracellular accumulation of DDP and Ola by specifically binding with heparanase (HPSE) to down-regulate PI3K/AKT/mTOR signaling pathway, and simultaneously served as a carrier combined with Ola to synergistically enhance the anti-proliferation ability of DDP for resistant ovarian cancer, thus achieving great therapeutic efficacy. Our DDP-Ola@HR could provide a simple and multifunctional combination strategy to trigger an anticipated cascading effect, thus effectively overcoming the chemo-resistance of ovarian cancer.

摘要

对化疗药物顺铂(DDP)的耐药性是卵巢癌化疗无效的主要原因。鉴于耐药性背后的复杂机制,基于阻断多种机制的联合治疗设计是一种合理的方法,可以协同提高治疗效果,有效克服癌症耐药性。在此,我们展示了一种多功能纳米粒子(DDP-Ola@HR),它可以使用肝素(HR)修饰的靶向配体 cRGD 肽作为纳米载体同时共递送 DDP 和奥拉帕利(Ola,DNA 损伤修复抑制剂),从而同时解决多种耐药机制,有效抑制 DDP 耐药卵巢癌的生长和转移。在联合策略中,肝素可以通过特异性结合透明质酸酶(HPSE)抑制多药耐药相关蛋白 2(MRP2)和 P-糖蛋白(P-gp)的功能,促进 DDP 和 Ola 的细胞内积累,下调 PI3K/AKT/mTOR 信号通路,同时作为载体与 Ola 结合,协同增强 DDP 对耐药卵巢癌细胞的增殖抑制能力,从而达到良好的治疗效果。我们的 DDP-Ola@HR 可以提供一种简单的多功能联合策略,引发预期的级联效应,从而有效克服卵巢癌的化疗耐药性。

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