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纳米药物在癌症治疗中的内吞作用和细胞器靶向。

Endocytosis and Organelle Targeting of Nanomedicines in Cancer Therapy.

机构信息

Institute of Medicinal Biotechnology, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, People's Republic of China.

出版信息

Int J Nanomedicine. 2020 Nov 25;15:9447-9467. doi: 10.2147/IJN.S274289. eCollection 2020.

DOI:10.2147/IJN.S274289
PMID:33268987
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7701161/
Abstract

Nanomedicines (NMs) have played an increasing role in cancer therapy as carriers to efficiently deliver therapeutics into tumor cells. For this application, the uptake of NMs by tumor cells is usually a prerequisite to deliver the cargo to intracellular locations, which mainly relies on endocytosis. NMs can enter cells through a variety of endocytosis pathways. Different endocytosis pathways exhibit different intracellular trafficking routes and diverse subcellular localizations. Therefore, a comprehensive understanding of endocytosis mechanisms is necessary for increasing cellular entry efficiency and to trace the fate of NMs after internalization. This review focuses on endocytosis pathways of NMs in tumor cells, mainly including clathrin- and caveolae-mediated endocytosis pathways, involving effector molecules, expression difference of those molecules between normal and tumor cells, as well as the intracellular trafficking route of corresponding endocytosis vesicles. Then, the latest strategies for NMs to actively employ endocytosis are described, including improving tumor cellular uptake of NMs by receptor-mediated endocytosis, transporter-mediated endocytosis and enabling drug activity by changing intracellular routes. Finally, active targeting strategies towards intracellular organelles are also mentioned. This review will be helpful not only in explicating endocytosis and the trafficking process of NMs and elucidating anti-tumor mechanisms inside the cell but also in rendering new ideas for the design of highly efficacious and cancer-targeted NMs.

摘要

纳米药物(NMs)作为将治疗剂有效递送至肿瘤细胞的载体,在癌症治疗中发挥着越来越重要的作用。对于这种应用,NMs 被肿瘤细胞摄取通常是将 cargo 递送至细胞内位置的前提,这主要依赖于内吞作用。NMs 可以通过多种内吞作用途径进入细胞。不同的内吞作用途径表现出不同的细胞内运输途径和不同的亚细胞定位。因此,全面了解内吞作用机制对于提高细胞进入效率和追踪内化后 NMs 的命运是必要的。

本综述重点介绍了 NMs 在肿瘤细胞中的内吞作用途径,主要包括网格蛋白和小窝蛋白介导的内吞作用途径,涉及效应分子、这些分子在正常和肿瘤细胞之间的表达差异,以及相应内吞小泡的细胞内运输途径。然后,描述了 NMs 主动利用内吞作用的最新策略,包括通过受体介导的内吞作用、转运体介导的内吞作用提高 NMs 的肿瘤细胞摄取,以及通过改变细胞内途径使药物活性化。最后,还提到了针对细胞内细胞器的主动靶向策略。

本综述不仅有助于阐明 NMs 的内吞作用和运输过程,阐明细胞内的抗肿瘤机制,而且为设计高效、靶向癌症的 NMs 提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/4e804f077b23/IJN-15-9447-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/5b56ccd0a4a8/IJN-15-9447-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/a485a44971f7/IJN-15-9447-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/4e804f077b23/IJN-15-9447-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/5b56ccd0a4a8/IJN-15-9447-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/a485a44971f7/IJN-15-9447-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/442f/7701161/4e804f077b23/IJN-15-9447-g0003.jpg

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