Department of Medical Imaging, Jinling Hospital, School of Medicine, Nanjing University, 210002 Jiangsu, China.
Department of Medical Imaging, Jinling Hospital, School of Medicine, Nanjing University, 210002 Jiangsu, China.
J Colloid Interface Sci. 2021 Dec;603:191-198. doi: 10.1016/j.jcis.2021.06.061. Epub 2021 Jun 12.
In this work, small self-assembled messenger RNA nanospheres (mRNA-NSs) were successfully prepared by rolling circle transcription on a constructed apoptin plasmid. The self-assembled mRNA-NSs have a uniform diameter of approximately 65 nm, good dispersity in solution, and efficient therapeutic apoptin expression ability. In addition, the mRNA-NSs have a high loading capacity of 8.2% for the antitumor drug doxorubicin (Dox), which can effectively deliver the loaded Dox into 4 T1 cells. Cellular experiments show that Dox-loaded self-assembled messenger RNA nanospheres (mRNA-NSs@Dox) can reduce the viability of 4 T1 breast cancer cells by significantly upregulating Bax protein, thereby inducing the activation of Caspase 3 in 4 T1 cells. In vivo experiments show that mRNA-NSs@Dox can effectively increase the necrosis of tumor tissue, reduce the expression of Ki67, and exhibit a synergistic gene-chemotherapy effect in breast cancer-bearing mice. Taken together, this study successfully prepared self-assembled apoptin messenger RNA nanospheres (mRNA-NSs), which can improve the expression of the therapeutic protein apoptin and exhibit excellent synergistic antitumor effects after loading Dox, providing new ideas for the gene treatment and chemotherapy of breast cancer.
在这项工作中,通过在构建的凋亡素质粒上进行滚环转录,成功制备了小的自组装信使 RNA 纳米球 (mRNA-NS)。自组装的 mRNA-NS 具有约 65nm 的均匀直径、良好的溶液分散性和高效的治疗性凋亡素表达能力。此外,mRNA-NS 对阿霉素 (Dox) 等抗肿瘤药物具有 8.2%的高载药量,可有效将负载的 Dox 递送至 4T1 细胞。细胞实验表明,负载 Dox 的自组装信使 RNA 纳米球 (mRNA-NS@Dox) 通过显著上调 Bax 蛋白,降低 4T1 乳腺癌细胞的活力,从而激活 4T1 细胞中的 Caspase 3。体内实验表明,mRNA-NS@Dox 能有效增加肿瘤组织坏死,降低 Ki67 的表达,并在荷瘤小鼠中表现出协同的基因化疗作用。综上所述,本研究成功制备了自组装的凋亡素信使 RNA 纳米球 (mRNA-NS),可提高治疗性蛋白凋亡素的表达,并在负载 Dox 后表现出优异的协同抗肿瘤作用,为乳腺癌的基因治疗和化疗提供了新的思路。