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超声敏感靶向脂质体作为协同治疗肝细胞癌的基因传递系统。

Ultrasound-Sensitive Targeted Liposomes as a Gene Delivery System for the Synergistic Treatment of Hepatocellular Carcinoma.

机构信息

Faculty of Chemistry, Northeast Normal University, Changchun, 130024, P. R. China.

出版信息

Small. 2024 Nov;20(47):e2406182. doi: 10.1002/smll.202406182. Epub 2024 Aug 27.

Abstract

Gene therapy and sonodynamic therapy, as emerging treatment methods, have great potential in cancer treatment. However, there are significant challenges in the in vivo delivery of genes and sonosensitizers during the treatment process, which ultimately affects the therapeutic outcome. In this study, an ultrasound-sensitive targeted liposome nanoparticle system (MLip) is developed to deliver the sonosensitizers and siRNA for the synergistic treatment of hepatocellular carcinoma. Generation of reactive oxygen species (ROS) by MLip can be initiated through ultrasound stimulation, leading to liposome rupture and release of the sonosensitizer and small interfering RNA (siRNA). Furthermore, ROS can disrupt lysosomal membranes, facilitating gene release for downregulating overexpressed antiapoptotic protein levels in cancer cells. Experimental results from in vitro and in vivo studies demonstrated the efficacy of synergistic treatment on hepatocellular carcinoma cells and the high biocompatibility of MLip under ultrasound stimulation. The advancement of this ultrasound-sensitive targeted gene delivery system shows potential as a versatile therapeutic platform that is easily operable, presenting a prospect for a synergistic treatment approach across various cancer types.

摘要

基因治疗和声动力学治疗作为新兴的治疗方法,在癌症治疗方面具有巨大的潜力。然而,在治疗过程中,基因和声敏剂的体内传递存在重大挑战,最终会影响治疗效果。在这项研究中,开发了一种超声敏感靶向脂质体纳米颗粒系统(MLip),用于递送声敏剂和 siRNA,以协同治疗肝细胞癌。MLip 通过超声刺激产生的活性氧(ROS)可以引发脂质体破裂,释放声敏剂和小干扰 RNA(siRNA)。此外,ROS 可以破坏溶酶体膜,促进基因释放,下调癌细胞中超表达的抗凋亡蛋白水平。体外和体内研究的实验结果表明,协同治疗对肝癌细胞的疗效以及 MLip 在超声刺激下的高生物相容性。这种超声敏感靶向基因传递系统的进步为多功能治疗平台提供了潜力,该平台易于操作,为各种癌症类型的协同治疗方法提供了前景。

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