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穿透细胞膜、热靶向与新型抗癌药物:热靶向弹性蛋白样多肽癌症治疗药物的研发

Penetrating the cell membrane, thermal targeting and novel anticancer drugs: the development of thermally targeted, elastin-like polypeptide cancer therapeutics.

作者信息

Ryu Jung Su, Kuna Marija, Raucher Drazen

机构信息

Department of Biochemistry, University of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216, USA.

出版信息

Ther Deliv. 2014 Apr;5(4):429-45. doi: 10.4155/tde.14.14.

Abstract

Therapeutic peptides offer important cancer treatment approaches. Designed to inhibit oncogenes and other oncoproteins, early therapeutic peptides applications were hampered by pharmacokinetic properties now addressed through tumor targeting strategies. Active targeting with environmentally responsive biopolymers or macromolecules enhances therapeutics accumulation at tumor sites; passive targeting with macromolecules, or liposomes, exploits angiogenesis and poor lymphatic drainage to preferentially accumulate therapeutics within tumors. Genetically engineered, thermally-responsive, elastin-like polypeptides use both strategies and cell-penetrating peptides to further intratumoral cell uptake. This review describes the development and application of cell-penetrating peptide-elastin-like polypeptide therapeutics for the thermally targeted delivery of therapeutic peptides.

摘要

治疗性肽提供了重要的癌症治疗方法。早期治疗性肽旨在抑制癌基因和其他癌蛋白,但其应用因药代动力学特性而受到阻碍,如今可通过肿瘤靶向策略来解决这一问题。利用环境响应性生物聚合物或大分子进行主动靶向可增强治疗剂在肿瘤部位的积累;利用大分子或脂质体进行被动靶向则利用肿瘤血管生成和淋巴引流不畅的特点,使治疗剂优先在肿瘤内积累。基因工程改造的、热响应性的、类弹性蛋白多肽同时运用了这两种策略以及细胞穿透肽,以进一步促进肿瘤内细胞摄取。本文综述了细胞穿透肽-类弹性蛋白多肽疗法在热靶向递送治疗性肽方面的发展与应用。

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