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多功能金纳米棒在低温光热相互作用下用于联合肿瘤饥饿和 RNA 干扰治疗。

Multifunctional gold nanorods in low-temperature photothermal interactions for combined tumor starvation and RNA interference therapy.

机构信息

Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu 610041, PR China; State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu, 610041, PR China.

Department of Immunology, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan 453000, PR China.

出版信息

Acta Biomater. 2023 Mar 15;159:324-337. doi: 10.1016/j.actbio.2023.01.036. Epub 2023 Jan 25.

Abstract

Collateral damage to healthy tissue, uneven heat distribution, inflammatory diseases, and tumor metastasis induction hinder the translation of high-temperature photothermal therapy (PTT) from bench to practical clinical applications. In this report, a multifunctional gold nanorod (GNR)-based nanosystem was designed by attaching siRNA against B7-H3 (B7-H3si), glucose oxidase (GOx), and hyaluronic acid (HA) for efficient low-temperature PTT. Herein, GOx can not only exhaust glucose to induce starvation therapy but also reduce the heat shock protein (HSP), realizing the ablation of tumors without damage to healthy tissues. Evidence shows that B7-H3, a type I transmembrane glycoprotein molecule, plays essential roles in growth, metastasis, and drug resistance. By initiating the downregulation of B7-H3 by siRNA, siRNA-GOx/GNR@HA NPs may promote the effectiveness of treatment. By targeting cluster of differentiation 44 (CD44) and depleting B7-H3 and HSPs sequentially, siRNA-GOx/GNR@HA NPs showed 12.9-fold higher lung distribution than siRNA-GOx/GNR NPs. Furthermore, 50% of A549-bearing mice in the siRNA-GOx/GNR NPs group survived over 50 days. Overall, this low-temperature phototherapeutic nanosystem provides an appropriate strategy for eliminating cancer with high treatment effectiveness and minimal systemic toxicity. STATEMENT OF SIGNIFICANCE: To realize efficient tumor ablation under mild low-temperature (42-45 ℃) and RNA interference simultaneously, here we developed a multifunctional gold nanorod (GNR)-based nanosystem (siRNA-GOx/GNR@HA NPs). This nanoplatform can significantly inhibit tumor cell proliferation and induce cell apoptosis by downregulation of HSP90α, HSP70, B7-H3, p-AKT, and p-ERK and upregulation of cleaved caspase-9 at mild low-temperature due to its superior tumor homing ability and the combined effect of photothermal effect, glucose deprivation-initiated tumor starvation, and B7-H3 gene silence effect. It is believed that this multifunctional low-temperature photothermal nanosystem with efficient and specific anticancer properties, shows a potential application in clinical tumor treatment.

摘要

健康组织的附带损伤、不均匀的热量分布、炎症性疾病和肿瘤转移诱导,阻碍了高温光热疗法(PTT)从实验室向实际临床应用的转化。在本报告中,通过附着针对 B7-H3(B7-H3si)、葡萄糖氧化酶(GOx)和透明质酸(HA)的 siRNA,设计了一种多功能金纳米棒(GNR)基纳米系统,用于高效低温 PTT。在这里,GOx 不仅可以耗尽葡萄糖以诱导饥饿疗法,还可以降低热休克蛋白(HSP),实现肿瘤消融而不损伤健康组织。有证据表明,B7-H3 是一种 I 型跨膜糖蛋白分子,在生长、转移和耐药性方面发挥着重要作用。通过启动 siRNA 下调 B7-H3,siRNA-GOx/GNR@HA NPs 可能会提高治疗效果。通过靶向 CD44 并依次耗尽 B7-H3 和 HSPs,siRNA-GOx/GNR@HA NPs 的肺部分布比 siRNA-GOx/GNR NPs 高 12.9 倍。此外,siRNA-GOx/GNR NPs 组中 50%的荷 A549 小鼠存活超过 50 天。总体而言,这种低温光疗纳米系统为消除癌症提供了一种合适的策略,具有较高的治疗效果和最小的全身毒性。

意义声明

为了实现在温和低温(42-45℃)下高效肿瘤消融和 RNA 干扰的双重效果,我们开发了一种多功能金纳米棒(GNR)基纳米系统(siRNA-GOx/GNR@HA NPs)。由于其优越的肿瘤归巢能力以及光热效应、葡萄糖剥夺诱导的肿瘤饥饿和 B7-H3 基因沉默效应的协同作用,该纳米平台能够在温和低温下通过下调 HSP90α、HSP70、B7-H3、p-AKT 和 p-ERK 以及上调 cleaved caspase-9,显著抑制肿瘤细胞增殖并诱导细胞凋亡。相信这种具有高效和特异性抗癌特性的多功能低温光热纳米系统在临床肿瘤治疗中具有潜在的应用前景。

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