Multifunctional polymer vesicles for cancer stem cells-targeted drug/siRNA therapy

Qiuming Liu, Jianzhong Du
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引用次数: 1

Abstract

Cancer stem cells (CSCs) are responsible for origin, growth, recurrence, and metastasis of tumor, and are closely linked to the failure of chemotherapy due to their self-renewal and multilineage differentiation capability with an innate resistance to cytotoxic agents. We have recently reported a novel EpCAM (epithelial cell adhesion molecule)-monoclonal-antibody-labeled CSCs-targeting, noncytotoxic and pH-sensitive block copolymer vesicle as a nanocarrier of anticancer drug and siRNA (to overcome CSCs drug resistance by silencing the expression of oncogenes). This vesicle shows high delivery efficacy of both doxorubicin hydrochloride (DOX·HCl) and siRNA to the CSCs. Furthermore, the DOX or siRNA loaded CSCs-targeting vesicles exhibited much better CSCs killing and tumor growth inhibition capabilities with much lower toxicity to normal cells (IC 50,DOX decreased by 80%) compared with non-CSCs-targeting vesicles. Overall, these vesicles have significant implications for overcoming CSCs chemo-resistance in cancer chemotherapy.
用于癌症干细胞靶向药物/siRNA治疗的多功能聚合物囊泡
肿瘤干细胞(Cancer stem cells, CSCs)与肿瘤的起源、生长、复发和转移有关,由于其自我更新和多谱系分化能力以及对细胞毒性药物的先天抗性,与化疗的失败密切相关。我们最近报道了一种新的EpCAM(上皮细胞粘附分子)-单克隆抗体标记的CSCs靶向,无细胞毒性和ph敏感的嵌段共聚物囊泡作为抗癌药物和siRNA的纳米载体(通过沉默癌基因的表达来克服CSCs的耐药性)。该囊泡显示盐酸阿霉素(DOX·HCl)和siRNA对CSCs的递送效率高。此外,与非CSCs靶向囊泡相比,负载DOX或siRNA的CSCs靶向囊泡表现出更好的CSCs杀伤和肿瘤生长抑制能力,对正常细胞的毒性低得多(IC 50,DOX降低80%)。总之,这些囊泡对于克服肿瘤化疗中CSCs的化疗耐药具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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