Cellular Membrane-Derived Nanovesicles Expressing hCD64 for Targeting Prostate Cancer.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Sehan Kim, Jeonghyeon Lee, Jaesung Park
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引用次数: 0

Abstract

Extracellular vesicles are ideal therapeutic potentiators for various diseases. However, they commonly lack targeting capability and are rapidly cleared by phagocytes. This requires appropriate administration at high doses, which can lead to toxic and adverse reactions. To overcome these limitations, we developed bleb nanovesicles containing human Fcγ receptor I (hCD64), known for their strong affinity to monomeric IgG. In this study, we focused on prostate cancer, which has a specific membrane antigen. We have utilized the hCD64-expressing bleb nanovesicles attaching anti-prostate-specific membrane antigen (PSMA) antibodies and confirmed their targeting ability in PSMA-related cell lines and prostate cancer xenograft models. Our findings underscore the promising potential of nanovesicle Fcγ receptor-IgG as a platform for cancer diagnosis and therapy systems, inspiring further research.

表达 hCD64 的细胞膜衍生纳米颗粒用于前列腺癌靶向治疗
细胞外囊泡是治疗各种疾病的理想增效剂。然而,它们通常缺乏靶向能力,会被吞噬细胞迅速清除。这就需要适当的高剂量给药,而高剂量给药可能会导致毒性和不良反应。为了克服这些局限性,我们开发了含有人 Fcγ 受体 I(hCD64)的蚕豆纳米囊泡,众所周知,人 Fcγ 受体 I 对单体 IgG 有很强的亲和力。在这项研究中,我们将重点放在前列腺癌上,因为前列腺癌具有特异性膜抗原。我们利用表达 hCD64 的吸附抗前列腺特异性膜抗原(PSMA)抗体的吸附纳米囊泡,证实了它们在 PSMA 相关细胞系和前列腺癌异种移植模型中的靶向能力。我们的研究结果凸显了纳米粒子 Fcγ 受体-IgG 作为癌症诊断和治疗系统平台的巨大潜力,激发了进一步研究的兴趣。
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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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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