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Manipulation of Mitophagy by All-in-One nanosensitizer augments sonodynamic glioma therapy

机译:一体化纳米敏化器增强Sonocynamic Glioma治疗的乳化物操纵

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摘要

Limited penetration of chemotherapeutic drugs through the blood brain barrier (BBB), and the increased chemo-resistance of glioma cells due to macroautophagy/autophagy, result in high tumor recurrence and extremely limited survival of glioma patients. Ultrasound-targeted microbubble destruction (UTMD) is a technique of transient and reversible BBB disruption, which greatly facilitates intracerebral drug delivery. In addition, sonodynamic therapy (SDT) based on ultrasound stimulation and a sonosensitizer, can be a safe and noninvasive strategy for treating glioma. We innovatively designed a smart “all-in-one” nanosensitizer platform by incorporating the sonoactive chlorin e6 (Ce6) and an autophagy inhibitor-hydroxychloroquine (HCQ) into angiopep-2 peptide-modified liposomes (designated as ACHL), which integrates multiple diagnostic and therapeutic functions. ACHL selectively accumulated in the brain tumors during the optimal time-window of transient UTMD-mediated BBB opening. The nanosensitizer then responded to a second ultrasonic stimulation, and simultaneously unloaded HCQ and generated ROS in the glioma cells. The sonotherapy triggered apoptosis as well as MAPK/p38-PINK1-PRKN-dependent mitophagy, in which the antioxidant relieved the sonotoxicity and MAPK/p38 activation, while the inhibition of MAPK/p38 attenuated the progression toward mitophagy by compromising redistribution of PRKN. Moreover, HCQ blocking autophagosome degradation, augmented intracellular ROS production and resulted in an oxidative-damage regenerative loop. ACHL-SDT treatment using this construct significantly inhibited the xenograft-tumor growth and prolonged the survival time of tumor-bearing mice, exhibiting an improved therapeutic efficiency. All together, we demonstrated a precision sonotherapy with simultaneous apoptosis induction and mitophagy inhibition, which served as an intelligently strategic sense of working alongside, providing new insights into the theranostics of brain tumors.
机译:化学治疗药物通过血脑屏障(BBB)的有限渗透,以及由于显微育苗/自噬引起的胶质瘤细胞的化学抗性增加,导致肿瘤复发性高,胶质瘤患者的存活率极为有限。超声靶向微泡破坏(UTMD)是一种瞬态和可逆的BBB破坏技术,这极大地促进了脑内药物递送。此外,基于超声刺激和超声溶剂的Sonocynamic Therapy(SDT)可以是治疗胶质瘤的安全和非侵入性的策略。我们通过将SonoactiveLlin E6(CE6)和自噬抑制剂 - 羟氯喹(HCQ)掺入Angiopep-2肽改性的脂质体(称为ACH1)中,创新设计了智能的“一体化”纳米溶剂平台,并将其集成了多种诊断和治疗功能。在瞬时UTMD介导的BBB开口的最佳时间窗口期间,在脑肿瘤中选择性地积累的ACH1。然后纳米溶剂剂响应第二超声刺激,并同时卸载HCQ并在胶质瘤细胞中产生ROS。声疗疗法触发了凋亡以及MAPK / P38-PINK1-PRKN依赖性乳化物,其中抗氧化剂缓解了超毒性和MAPK / P38激活,而MAPK / P38的抑制通过损害PRKN的再分配而衰减了对乳化物的进展。此外,HCQ阻断自噬体降解,增强细胞内ROS产生并导致氧化损伤的再生环。使用该构建体的ACHL-SDT治疗显着抑制异种移植肿瘤的生长,延长了肿瘤小鼠的存活时间,表现出改善的治疗效率。一切都在一起,展示了一种具有同时细胞凋亡诱导和水肿抑制的精密声学,这是一种智能战略的工作感,为脑肿瘤的治疗有新的见解。

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