Laboratory of Molecular Pharmacology, Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan Province, China.
Nanoscale. 2017 Sep 28;9(37):13879-13904. doi: 10.1039/c7nr04959e.
Since its initial identification, tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) has been shown to be capable of selectively inducing apoptosis in cancer cells. However, translation of the encouraging preclinical studies of this cytokine into the clinic has been restricted by its extremely short half-life, the presence of resistant cancer cell populations, and its inefficient in vivo delivery. Recently, there has been exceptional progress in developing novel formulations to increase the circulatory half-life of TRAIL and new combinations to treat cancers that are resistant to TRAIL. In particular, TRAIL-based nanotherapies offer the potential to improve the stability of TRAIL and prolong its half-life in plasma, to specifically deliver TRAIL to a particular target site, and to overcome resistance to TRAIL. The aim of this review is to provide an overview of the state-of-the art drug delivery systems that are currently being tested or developed to improve the biological attributes of TRAIL-based therapies.
自最初发现以来,肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)已被证明能够选择性地诱导癌细胞凋亡。然而,这种细胞因子的令人鼓舞的临床前研究转化为临床应用受到其极短的半衰期、存在耐药癌细胞群体以及其体内递送效率低下的限制。最近,在开发新制剂以增加 TRAIL 的循环半衰期和新组合以治疗对 TRAIL 耐药的癌症方面取得了非凡的进展。特别是,基于 TRAIL 的纳米疗法有可能提高 TRAIL 的稳定性并延长其在血浆中的半衰期,将 TRAIL 特异性递送至特定靶位,并克服对 TRAIL 的耐药性。本文旨在综述目前正在测试或开发中的改善基于 TRAIL 的治疗方法的生物特性的最新药物传递系统。