Institute for Drug Research, School of Pharmacy, The Hebrew University, Jerusalem, 91120, Israel.
J Inorg Biochem. 2019 Feb;191:77-84. doi: 10.1016/j.jinorgbio.2018.11.008. Epub 2018 Nov 15.
Pt(IV) complexes act as prodrugs that are activated inside cancer cells releasing cytotoxic Pt(II) drugs such as cisplatin as well as two axial ligands. These ligands can be used to confer favorable pharmacological properties to the prodrug. They can be innocent spectators, targeting agents or bioactive moieties. When the ligands are bioactive moieties such as enzyme inhibitors or antiproliferative agents, the prodrug attacks several cellular targets at the same time acting as a multi-action prodrug. These compounds are very potent and often overcome resistance to cisplatin. Despite solid rationalization and careful design, often there is no correlation between the ability of the bioactive ligand to inhibit the target enzyme and the cytotoxicity. This might be because most bioactive ligands affect several cellular functions and not only the ones they were designed to inhibit. Thus, even "dual action" prodrugs might in reality be multi-action prodrugs. This class of multi-action Pt(IV) prodrugs seems to have great potential in the attempts to overcome resistance.
Pt(IV) 配合物作为前药,在癌细胞内被激活,释放出细胞毒性的 Pt(II) 药物,如顺铂以及两个轴向配体。这些配体可用于赋予前药有利的药理学性质。它们可以是无辜的旁观者、靶向剂或生物活性部分。当配体是生物活性部分,如酶抑制剂或抗增殖剂时,前药会同时攻击多个细胞靶标,充当多作用前药。这些化合物非常有效,常常克服了对顺铂的耐药性。尽管有合理的推理和精心的设计,但生物活性配体抑制靶酶的能力与细胞毒性之间通常没有相关性。这可能是因为大多数生物活性配体影响多种细胞功能,而不仅仅是它们被设计用来抑制的功能。因此,即使是“双重作用”前药实际上也可能是多作用前药。这类多作用 Pt(IV) 前药在克服耐药性的尝试中似乎具有很大的潜力。