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Targeted Delivery of siRNA Lipoplexes to Cancer Cells Using Macrophage Transient Horizontal Gene Transfer

机译:使用巨噬细胞瞬时水平基因转移靶向递送siRNA脂质体至癌细胞

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摘要

Delivery of nucleic acids into solid tumor environments remains a pressing challenge. This study examines the ability of macrophages to horizontally transfer small interfering RNA (siRNA) lipoplexes to cancer cells. Macrophages are a natural candidate for a drug carrier because of their ability to accumulate at high densities into many cancer types, including, breast, prostate, brain, and colon cancer. Here, it is demonstrated that macrophages can horizontally transfer siRNA to cancer cells during in vitro coculture. The amount of transfer can be dosed depending on the amount of siRNA loaded and total number of macrophages delivered. Macrophages loaded with calcium integrin binding protein‐1 (CIB1)‐siRNA result in decreased tumorsphere growth and decreased mRNA expression of CIB1 and KI67 in MDA‐MB‐468 human breast cancer cells. Adoptive transfer of macrophages transfected with CIB1‐siRNA localizes to the orthotopic MDA‐MB‐468 tumor. Furthermore, it is reported that macrophage activation can modulate this transfer process as well as intracellular trafficking protein . As macrophages are heavily involved in tumor progression, understanding how to use macrophages for drug delivery can substantially benefit the treatment of tumors.
机译:将核酸递送到实体瘤环境中仍然是紧迫的挑战。这项研究检查了巨噬细胞将小干扰RNA(siRNA)脂质复合物水平转移到癌细胞的能力。巨噬细胞是药物载体的天然候选物,因为它们具有高密度积聚成多种癌症类型的能力,包括乳腺癌,前列腺癌,脑癌和结肠癌。在此,证明了巨噬细胞可以在体外共培养过程中将siRNA水平转移到癌细胞中。可以根据转移的siRNA的量和所递送的巨噬细胞的总数确定转移的剂量。载有钙整合蛋白结合蛋白-1(CIB1)-siRNA的巨噬细胞可导致MDA-MB-468人乳腺癌细胞中肿瘤球的生长减少以及CIB1和KI67的mRNA表达下降。用CIB1-siRNA转染的巨噬细胞的过继转移定位于原位MDA-MB-468肿瘤。此外,据报道巨噬细胞活化可以调节该转移过程以及细胞内运输蛋白。由于巨噬细胞大量参与肿瘤的进展,因此了解如何使用巨噬细胞进行药物递送可以大大有益于肿瘤的治疗。

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