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An Oligopeptide Ligand-Mediated Therapeutic Gene Nanocomplex for Liver Cancer-Targeted Therapy

机译:寡肽配体介导的肝癌靶向治疗基因纳米复合物

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The epidermal growth factor receptor (EGFR) is over-expressed in a wide variety of epithelial-derived cancer cells. In this study, EGFR-targeted gene carriers were designed to complex AChE gene for effective treatment of EGFR-positive liver cancers. Different amounts of target ligand YC21 (an oligopeptide composed of 21 amino acid units) were coupled with the PEI_(600)-CD (PC) vectors composed of β-cyclodextrin (β-CD) and low-molecular-weight polyethylenimine (PEI, Mw 600) to form the EGFR-targeted gene vectors (termed as YPCs). The YPC vector possessed the highly efficient gene delivery ability to the EGFR-positive liver cancer cells. YPCs could effectively promote AChE gene expression. By investigating anticancer efficacy via EGFR-positive liver cancer cells, it was found that the YPC/AChE complexes produced excellent gene transfection abilities and effectively promoted the inhibition of tumor growth in vivo. Such target peptide-mediated therapeutic gene complexes should have great potential applications in cancer therapy.
机译:表皮生长因子受体(EGFR)在多种上皮来源的癌细胞中过表达。在这项研究中,针对EGFR的基因载体被设计为复合AChE基因,以有效治疗EGFR阳性肝癌。将不同数量的目标配体YC21(由21个氨基酸单元组成的寡肽)与PEI_(600)-CD(PC)载体偶联,该载体由β-环糊精(β-CD)和低分子量聚乙烯亚胺(PEI, Mw 600)形成EGFR靶向的基因载体(称为YPC)。 YPC载体具有向EGFR阳性肝癌细胞的高效基因传递能力。 YPCs可以有效地促进AChE基因表达。通过研究EGFR阳性肝癌细胞的抗癌功效,发现YPC / AChE复合物产生了出色的基因转染能力,并有效地促进了体内肿瘤生长的抑制。这种靶肽介导的治疗基因复合物在癌症治疗中应具有巨大的潜在应用。

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