Moores Cancer Center, University of California San Diego, La Jolla, California 92037, United States.
Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555, United States.
Curr Med Chem. 2021;28(19):3683-3712. doi: 10.2174/0929867327666201027152737.
Aldose Reductase (AR) is an enzyme that converts glucose to sorbitol during the polyol pathway of glucose metabolism. AR has been shown to be involved in the development of secondary diabetic complications due to its involvement in causing osmotic as well as oxidative stress. Various AR inhibitors have been tested for their use to treat secondary diabetic complications, such as retinopathy, neuropathy, and nephropathy in clinical studies. Recent studies also suggest the potential role of AR in mediating various inflammatory complications. Therefore, the studies on the development and potential use of AR inhibitors to treat inflammatory complications and cancer besides diabetes are currently on the rise. Further, genetic mutagenesis studies, computer modeling, and molecular dynamics studies have helped design novel and potent AR inhibitors. This review discussed the potential new therapeutic use of AR inhibitors in targeting inflammatory disorders and cancer besides diabetic complications. Further, we summarized studies on how AR inhibitors have been designed and developed for therapeutic purposes in the last few decades.
醛糖还原酶(AR)是一种在葡萄糖代谢的多元醇途径中将葡萄糖转化为山梨醇的酶。由于其参与引起渗透和氧化应激,AR 已被证明与继发性糖尿病并发症的发展有关。在临床研究中,已经测试了各种 AR 抑制剂用于治疗继发性糖尿病并发症,如视网膜病变、神经病和肾病。最近的研究还表明 AR 在介导各种炎症并发症中的潜在作用。因此,目前关于开发和潜在使用 AR 抑制剂治疗炎症并发症和癌症(除糖尿病外)的研究正在增加。此外,遗传诱变研究、计算机建模和分子动力学研究有助于设计新型强效 AR 抑制剂。这篇综述讨论了 AR 抑制剂在除糖尿病并发症以外的靶向炎症性疾病和癌症方面的潜在新治疗用途。此外,我们总结了过去几十年中为治疗目的而设计和开发 AR 抑制剂的研究。