Department of Biochemistry, University at Buffalo, Buffalo, New York
J Pharmacol Exp Ther. 2023 Jul;386(1):1-3. doi: 10.1124/jpet.123.001645.
Divalent metal transporter 1 (DMT1) is the major importer of ferrous iron at the apical surface of enterocytes in the duodenum. Multiple groups have tried to design specific inhibitors for DMT1 both to study its contributions to iron (and metal ion) homeostasis and to provide a pharmacological means to treat iron overload disorders like hereditary hemochromatosis and thalassemias. This task faces challenges because many tissues express DMT1 and DMT1 transports other metals adding to standard risks in making specific inhibitors. Xenon Pharmaceuticals have published several papers on their efforts. Their latest paper in this issue of the journal culminates their efforts with compounds named XEN601 and XEN602 but implies that these very effective inhibitors have sufficient toxicity for them to halt development. This Viewpoint evaluates their efforts and briefly considers alternative routes to the goal. SIGNIFICANCE STATEMENT: This Viewpoint briefly reviews the paper on inhibitors of DMT1 that appears in this issue of the journal and commends the effort and research utility of those developed by Xenon. The inhibitors have proven to be valuable research tools for studying metal ion homeostasis particularly for iron. If Xenon is ceasing to try to develop them for treatment of iron overload disorders, then new alternatives need to come to the fore.
二价金属转运蛋白 1(DMT1)是十二指肠肠上皮细胞顶端表面亚铁离子的主要摄取体。许多研究团队尝试设计 DMT1 的特异性抑制剂,既用于研究其对铁(和金属离子)稳态的贡献,也用于提供治疗铁过载疾病(如遗传性血色素沉着症和地中海贫血症)的药理学手段。这项任务面临挑战,因为许多组织都表达 DMT1,而且 DMT1 还转运其他金属,这增加了设计特异性抑制剂的标准风险。 Xenon Pharmaceuticals 已经在他们的期刊上发表了几篇关于他们努力的论文。他们在本期期刊上的最新论文总结了他们用名为 XEN601 和 XEN602 的化合物的努力,但暗示这些非常有效的抑制剂毒性太大,以至于他们停止了开发。本观点评估了他们的努力,并简要考虑了实现目标的替代途径。意义陈述:本观点简要回顾了本期期刊上关于 DMT1 抑制剂的论文,并赞扬了 Xenon 开发的抑制剂的努力和研究效用。这些抑制剂已被证明是研究金属离子稳态的有价值的研究工具,特别是对铁。如果 Xenon 停止尝试用它们来治疗铁过载疾病,那么就需要新的替代品出现。