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利用细菌毒素转位机制的癌症药物递送系统

Cancer Drug Delivery Systems Using Bacterial Toxin Translocation Mechanisms.

作者信息

Yin Linxiang, Thaker Hatim

机构信息

Department of Urology, Boston Children's Hospital, Boston, MA 02115, USA.

Department of Surgery, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Bioengineering (Basel). 2023 Jul 7;10(7):813. doi: 10.3390/bioengineering10070813.

Abstract

Recent advances in targeted cancer therapy hold great promise for both research and clinical applications and push the boundaries in finding new treatments for various currently incurable cancers. However, these therapies require specific cell-targeting mechanisms for the efficient delivery of drug cargo across the cell membrane to reach intracellular targets and avoid diffusion to unwanted tissues. Traditional drug delivery systems suffer from a limited ability to travel across the barriers posed by cell membranes and, therefore, there is a need for high doses, which are associated with adverse reactions and safety concerns. Bacterial toxins have evolved naturally to specifically target cell subtypes via their receptor binding module, penetrating the cell membrane efficiently through the membrane translocation process and then successfully delivering the toxic cargo into the host cytosol. They have, thus, been harnessed for the delivery of various drugs. In this review, we focus on bacterial toxin translocation mechanisms and recent progress in the targeted delivery systems of cancer therapy drugs that have been inspired by the receptor binding and membrane translocation processes of the anthrax toxin protective antigen, diphtheria toxin, and exotoxin A. We also discuss the challenges and limitations of these studies that should be addressed before bacterial toxin-based drug delivery systems can become a viable new generation of drug delivery approaches in clinical translation.

摘要

靶向癌症治疗的最新进展在研究和临床应用方面都具有巨大潜力,推动了为各种目前无法治愈的癌症寻找新治疗方法的边界。然而,这些疗法需要特定的细胞靶向机制,以便将药物有效递送至细胞膜穿过细胞到达细胞内靶点,并避免扩散到不需要的组织。传统的药物递送系统穿越细胞膜所构成屏障的能力有限,因此需要高剂量药物,而这会带来不良反应和安全问题。细菌毒素通过其受体结合模块自然进化以特异性靶向细胞亚型,通过膜转位过程有效穿透细胞膜,然后成功将有毒物质递送至宿主细胞质中。因此,它们已被用于递送各种药物。在本综述中,我们重点关注细菌毒素转位机制以及受炭疽毒素保护性抗原、白喉毒素和外毒素A的受体结合及膜转位过程启发的癌症治疗药物靶向递送系统的最新进展。我们还讨论了这些研究在基于细菌毒素的药物递送系统成为临床转化中可行的新一代药物递送方法之前应解决的挑战和局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3452/10376142/d4fb2e101099/bioengineering-10-00813-g001.jpg

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