Lee Gil Ya Cancer and Diabetes Institute, Gachon University, Incheon 21999, Republic of Korea.
Nanotechnology. 2017 Nov 17;28(46):465102. doi: 10.1088/1361-6528/aa8c31. Epub 2017 Oct 20.
Although activating apoptosis in cancer cells by targeting the mitochondria is an effective strategy for cancer therapy, insufficient targeting of the mitochondria in cancer cells restricts the availability in clinical treatment. Here, we report on a polyethylene glycol-coated carbon nanotube (CNT)-ABT737 nanodrug that improves the mitochondrial targeting of lung cancer cells. The polyethylene glycol-coated CNT-ABT737 nanodrug internalized into the early endosomes via macropinocytosis and clathrin-mediated endocytosis in advance of early endosomal escape and delivered into the mitochondria. Cytosol release of the nanodrug led to apoptosis of lung cancer cells by abruption of the mitochondrial membrane potential, inducing Bcl-2-mediated apoptosis and generating intracellular reactive oxygen species. As such, this study provides an effective strategy for increasing the anti-lung cancer efficacy by increasing mitochondria accumulation rate of cytosol released anticancer nanodrugs.
虽然通过靶向线粒体在癌细胞中激活细胞凋亡是癌症治疗的有效策略,但癌细胞中线粒体的靶向不足限制了其在临床治疗中的应用。在这里,我们报告了一种聚乙二醇包覆的碳纳米管(CNT)-ABT737 纳米药物,它可以提高肺癌细胞的线粒体靶向性。聚乙二醇包覆的 CNT-ABT737 纳米药物通过巨胞饮作用和网格蛋白介导的内吞作用提前内化到早期内体中,然后逃脱早期内体并递送到线粒体。纳米药物的细胞质释放通过线粒体膜电位的突然中断导致肺癌细胞凋亡,诱导 Bcl-2 介导的凋亡并产生细胞内活性氧。因此,这项研究提供了一种通过增加细胞质释放的抗癌纳米药物的线粒体积累率来提高抗肺癌疗效的有效策略。