CICS-UBI-Health Sciences Research Centre, University of Beira Interior, Av. Infante D. Henrique. 6200-506, Covilhã, Portugal.
UDI-IPG-Unidade de Investigação Para o Desenvolvimento Do Interior, Instituto Politécnico da Guarda, Guarda, Portugal.
J Physiol Biochem. 2023 Aug;79(3):467-487. doi: 10.1007/s13105-023-00957-1. Epub 2023 Mar 30.
Drug efficacy is dependent on the pharmacokinetics and pharmacodynamics of therapeutic agents. Tight junctions, detoxification enzymes, and drug transporters, due to their localization on epithelial barriers, modulate the absorption, distribution, and the elimination of a drug. The epithelial barriers which control the pharmacokinetic processes are sex steroid hormone targets, and in this way, sex hormones may also control the drug transport across these barriers. Thus, sex steroids contribute to sex differences in drug resistance and have a relevant impact on the sex-related efficacy of many therapeutic drugs. As a consequence, for the further development and optimization of therapeutic strategies, the sex of the individuals must be taken into consideration. Here, we gather and discuss the evidence about the regulation of ATP-binding cassette transporters by sex steroids, and we also describe the signaling pathways by which sex steroids modulate ATP-binding cassette transporters expression, with a focus in the most important ATP-binding cassette transporters involved in multidrug resistance.
药物疗效取决于治疗药物的药代动力学和药效学。紧密连接、解毒酶和药物转运体由于其在上皮屏障上的定位,调节药物的吸收、分布和消除。控制药代动力学过程的上皮屏障是性激素激素的靶标,因此性激素也可以控制药物穿过这些屏障的转运。因此,性激素导致药物耐药性的性别差异,并对许多治疗药物的性别相关疗效有相关影响。因此,为了进一步开发和优化治疗策略,必须考虑个体的性别。在这里,我们收集并讨论了关于性激素对 ABC 转运蛋白调节的证据,还描述了性激素调节 ABC 转运蛋白表达的信号通路,重点是涉及多药耐药的最重要的 ABC 转运蛋白。