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双药配对聚前药纳米诊疗剂通过温和的光热鸡尾酒化疗逆转多药耐药癌症。

Dual drug-paired polyprodrug nanotheranostics reverse multidrug resistant cancers via mild photothermal-cocktail chemotherapy.

机构信息

School of Chemistry and Chemical Engineering, Shanghai Key Laboratory of Electrical Insulation and Thermal Aging, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.

Department of Obstetrics and Gynecology, Shanghai Fengxian Central Hospital, Southern Medical University, Shanghai 201499, P. R. China.

出版信息

J Mater Chem B. 2019 Sep 11;7(35):5306-5319. doi: 10.1039/c9tb01368g.

Abstract

Combating multidrug resistance (MDR) of tumors is still challenging for clinical chemotherapy, cocktail chemotherapy (CCT), and currently widely-studied nanodrug-based treatments. Inspired by different MDR-overcoming and antitumor mechanisms of CCT and photothermal therapy (PT), a dual drug-paired polyprodrug nanoparticle (PDCN25-CDDP) was constructed to achieve the combination therapy PT-CCT for reversing MDR and combating multidrug resistant cancers. The PT-CCT treatment can greatly downregulate the P-gp expression level and achieve utmost MDR-reversal and antitumor efficacy by both a cocktail effect of CCT and a synergistic effect of CCT with PT; meanwhile, PT can inhibit the expression of heat shock protein 90 and enhance the thermosensitivity of cancer cells. Upon NIR irradiation, PDCN25-CDDPin vivo produced a selective tumor accumulation effect and relatively deep tumor penetration, as evidenced by fluorescent and photoacoustic imaging and CLSM. The mild PT-CCT treatment completely eradicated MCF-7/ADR and OVCAR-3/DDP tumors without skin damage or tumor recurrence for 30 days, exhibiting synergistic MDR-reversal and superior antitumor efficacy in vivo. Importantly, this work provides an innovative strategy for reversing MDR and combating DOX-resistant breast and CDDP-resistant ovarian cancers.

摘要

针对肿瘤的多药耐药性(MDR)仍然是临床化疗、联合化疗(CCT)以及当前广泛研究的基于纳米药物的治疗方法面临的挑战。受 CCT 和光热疗法(PT)不同的克服 MDR 和抗肿瘤机制的启发,构建了一种双重药物配对的多前药纳米粒子(PDCN25-CDDP),以实现逆转 MDR 和治疗多药耐药性癌症的联合治疗 PT-CCT。PT-CCT 治疗可以通过 CCT 的鸡尾酒效应和 CCT 与 PT 的协同效应,极大地下调 P-糖蛋白表达水平,实现最大程度的 MDR 逆转和抗肿瘤疗效;同时,PT 可以抑制热休克蛋白 90 的表达,增强癌细胞的热敏感性。在近红外光照射下,PDCN25-CDDP 在体内产生了选择性的肿瘤积累效应和相对较深的肿瘤穿透,荧光和光声成像以及 CLSM 均证实了这一点。温和的 PT-CCT 治疗完全根除了 MCF-7/ADR 和 OVCAR-3/DDP 肿瘤,没有皮肤损伤或肿瘤复发,持续 30 天,在体内具有协同的 MDR 逆转和优异的抗肿瘤疗效。重要的是,这项工作为逆转 MDR 和治疗 DOX 耐药性乳腺癌和 CDDP 耐药性卵巢癌提供了一种创新策略。

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