Univ Rennes, Inserm, EHESP, Irset (Institut De Recherche En Santé, Environnement Et Travail) - UMR_S 1085, Rennes, France.
Univ Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut De Recherche En Santé, Environnement Et Travail) - UMR_S 1085, Rennes, France.
Expert Opin Drug Metab Toxicol. 2021 Mar;17(3):259-271. doi: 10.1080/17425255.2021.1862084. Epub 2021 Jan 11.
: Janus kinase inhibitors (JAKinibs) constitute an emerging and promising pharmacological class of anti-inflammatory or anti-cancer drugs, used notably for the treatment of rheumatoid arthritis and some myeloproliferative neoplasms.: This review provides an overview of the interactions between marketed JAKinibs and major uptake and efflux drug transporters. Consequences regarding pharmacokinetics, drug-drug interactions and toxicity are summarized.: JAKinibs interact with transporters in various ways, as inhibitors or as substrates of transporters or as regulators of transporter expression. This may theoretically result in drug-drug interactions (DDIs), with JAKinibs acting as perpetrators or as victims, or in toxicity, via impairment of thiamine transport. Clinical significance in terms of DDIs for JAKinib-transporter interactions remains however poorly documented. In this context, the unbound concentration of JAKinibs is likely a key parameter to consider for evaluating the clinical relevance of JAKinibs-mediated transporter inhibition. Additionally, the interplay with drug metabolism as well as possible interactions with transporters of emerging importance and time-dependent inhibition have to be taken into account. The role drug transporters may play in controlling cellular JAKinib concentrations and efficacy in target cells is also an issue of interest.
: 酪氨酸激酶抑制剂(JAKinibs)是一类新兴且有前景的抗炎或抗癌药物,主要用于治疗类风湿关节炎和一些骨髓增殖性肿瘤。 : 本文综述了已上市 JAKinibs 与主要摄取和外排药物转运体之间的相互作用。对药代动力学、药物相互作用和毒性的影响进行了总结。 : JAKinibs 以多种方式与转运体相互作用,作为转运体的抑制剂或底物,或作为转运体表达的调节剂。这可能会导致药物相互作用(DDI),JAKinibs 作为肇事者或受害者,或通过干扰硫胺素转运而导致毒性。然而,JAKinib-转运体相互作用的药物相互作用在临床上的意义记录甚少。在这种情况下,考虑 JAKinib 介导的转运体抑制的临床相关性,JAKinib 的游离浓度可能是一个关键参数。此外,还需要考虑与药物代谢的相互作用以及新兴重要的转运体和时间依赖性抑制的可能相互作用。药物转运体在控制细胞内 JAKinib 浓度和靶细胞功效方面的作用也是一个值得关注的问题。