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Tailored Lipoprotein‐Like miRNA Delivery Nanostructure Suppresses Glioma Stemness and Drug Resistance through Receptor‐Stimulated Macropinocytosis

机译:定制的类似脂蛋白的miRNA递送纳米结构通过受体刺激的巨胞吞作用抑制神经胶质瘤的干性和耐药性。

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摘要

Glioma initiating cells (GICs) function as the seed for the propagation and relapse of glioma. Designing a smart and efficient strategy to target the GICs and to suppress the multiple signaling pathways associated with stemness and chemoresistance is essential to achieving a cancer cure. Inspired by the metabolic difference in endocytosis between GICs, differentiated glioma cells, and normal cells, a tailored lipoprotein‐like nanostructure is developed to amplify their internalization into GICs through receptor‐stimulated macropinocytosis. As CXCR4 is highly expressed on GICs and glioma tumor sites, meanwhile, the activation of CXCR4 induces the receptor‐stimulated macropinocytosis pathway in GICs, this CXCR4 receptor‐stimulated lipoprotein‐like nanoparticle (SLNP) achieves efficient accumulation in GICs in vitro and in vivo. By carrying microRNA‐34a in the core, this tailored SLNP reduces sex‐determining region Y‐box 2 and Notch1 expression, powerfully inhibits GICs stemness and chemoresistance, and significantly prolongs the survival of GICs‐bearing mice. Taken together, a tailored lipoprotein‐based nanostructure realizes efficient GICs accumulation and therapeutic effect through receptor‐stimulated macropinocytosis, providing a powerful nanoplatform for RNA interference drugs to combat glioma.
机译:胶质瘤起始细胞(GIC)充当神经胶质瘤的繁殖和复发的种子。设计一种靶向GIC并抑制与干性和化学抗性相关的多种信号传导途径的明智而有效的策略对于实现癌症治愈至关重要。受GIC,分化的神经胶质瘤细胞和正常细胞之间内吞作用代谢差异的启发,开发了定制的脂蛋白样纳米结构,以通过受体刺激的巨胞饮作用放大其内在化的GIC。由于CXCR4在GIC和神经胶质瘤肿瘤位点上高表达,同时CXCR4的激活诱导GIC中受体刺激的巨胞饮途径,这种CXCR4受体刺激的脂蛋白样纳米颗粒(SLNP)在GIC中实现了体内和体外的有效积累。 。通过在核心中携带microRNA-34a,这种定制的SLNP减少了性别决定区域Y-box 2和Notch1的表达,有力地抑制了GIC的干性和化学抗性,并显着延长了带有GIC的小鼠的存活期。结合在一起,量身定制的基于脂蛋白的纳米结构通过受体刺激的巨胞饮作用实现了有效的GIC积累和治疗效果,为RNA干扰药物提供了强大的纳米平台来对抗神经胶质瘤。

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