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Pulsed-wave Ultrasound Hyperthermia Enhanced Nanodrug Delivery Combined with Chloroquine Exerts Effective Antitumor Response and Postpones Recurrence

机译:脉冲波超声热疗增强型纳米树脂递送联合氯喹施加有效的抗肿瘤反应和推迟复发

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Autophagy is found to serve as a surviving mechanism for cancer cells. Inhibiting autophagy has been considered as an adjuvant anti-cancer strategy. In this study, we investigated the anti-tumor effect of combining pulsed-wave ultrasound hyperthermia (pUH) enhanced PEGylated liposomal doxorubicin (PLD) delivery with an autophagy inhibitor chloroquine (CQ). BALB/c mice bearing subcutaneous 4T1 tumor received intravenous injection of PLD (10?mg/kg) plus 15-minute on-tumor pUH on Day 5 after tumor implantation and were then fed with CQ (50?mg/kg daily) thereafter. Prolonged suppression of tumor growth was attained with PLD?+?pUH?+?CQ treatment, whereas in PLD?+?pUH group tumors quickly recurred after an initial inhibition. Treatment with CQ monotherapy had no benefit compared to the control group. Immunohistochemical staining and Western blotting showed that autophagy of cancer cells was blocked for the mice receiving CQ. It indicates that PLD?+?pUH?+?CQ is a promising strategy to treat cancer for a long-term inhibition.
机译:发现自噬是癌细胞的存活机制。抑制自噬被认为是佐剂抗癌策略。在这项研究中,我们研究了将脉冲波超声热疗(PUH)增强的聚乙二醇化脂质体DOXORUBICIN(PLD)递送的抗肿瘤作用用自噬抑制剂氯喹(CQ)。 BALB / C小鼠携带皮下4T1肿瘤,在肿瘤植入后第5天接受静脉注射PLD(10?Mg / kg)加15分钟的肿瘤PUH,然后将其后用CQ(50×mg / kg每日)加入。延长抑制肿瘤生长肿瘤α+?+ + +?CQ治疗,而在PLD?+ +瘤肿瘤中急于抑制后迅速重复。与对照组相比,用CQ单疗法的治疗无益。免疫组织化学染色和蛋白质印迹显示,接受CQ的小鼠抑制癌细胞的自噬。它表明PLD?+?苏·+?CQ是治疗长期抑制的有希望的策略。

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