Institute for Drug Research, School of Pharmacy, The Hebrew University of Jerusalem, Jerusalem 9112102, Israel.
J Inorg Biochem. 2021 Apr;217:111353. doi: 10.1016/j.jinorgbio.2020.111353. Epub 2021 Jan 7.
Pt(IV) complexes are designed as prodrugs that are intended to overcome resistance. Pt(IV) prodrugs are activated inside cancer cells releasing cytotoxic Pt(II) drugs as well as two axial ligands that can be used to confer favorable pharmacological properties to the prodrug. The ligands can be innocent spectators, cancer targeting agents or bioactive moieties. The choice of axial ligands determines the chemical and pharmacological properties of the prodrugs. Over the years, several approaches were employed in attempts to increase the selectivity of the prodrugs to cancer cells and to utilize multi-action prodrugs to overcome resistance. In this review, we critically examine several of these approaches in order to evaluate the validity of some of the working hypotheses that are driving the current research.
Pt(IV) 配合物被设计为前药,旨在克服耐药性。Pt(IV) 前药在癌细胞内被激活,释放细胞毒性 Pt(II) 药物以及两个轴向配体,这些配体可用于赋予前药有利的药理学性质。配体可以是无辜的旁观者、癌症靶向剂或生物活性部分。轴向配体的选择决定了前药的化学和药理学性质。多年来,人们采用了几种方法来提高前药对癌细胞的选择性,并利用多作用前药来克服耐药性。在这篇综述中,我们批判性地研究了其中的几种方法,以评估当前研究中一些驱动因素的有效性。