Reckzeh Elena S, Waldmann Herbert
Department of Chemical Biology Max Planck Institute of Molecular Physiology Otto-Hahn-Str. 11 44227 Dortmund Germany.
Department Chemistry and Chemical Biology TU Dortmund University Otto-Hahn-Str. 4a 44227 Dortmund Germany.
European J Org Chem. 2020 May 3;2020(16):2321-2329. doi: 10.1002/ejoc.201901353. Epub 2019 Nov 28.
The discovery of novel compound classes endowed with biological activity is at the heart of chemical biology and medicinal chemistry research. This enables novel biological insights and inspires new approaches to the treatment of diseases. Cancer cells frequently exhibit altered glycolysis and glucose metabolism and an increased glucose demand. Thus, targeting glucose uptake and metabolism may open up novel opportunities for the discovery of compounds that differentiate between normal and malignant cells. This review discusses the different chemical approaches to the development of novel inhibitors of glucose uptake through facilitative glucose transporters (GLUTs), and focusses on the most advanced and potent inhibitor classes known to date. GLUT inhibitors may find application not only in the treatment of cancer, but also of other proliferative diseases that exhibit glucose addiction.
发现具有生物活性的新型化合物类别是化学生物学和药物化学研究的核心。这有助于获得新的生物学见解,并激发治疗疾病的新方法。癌细胞经常表现出糖酵解和葡萄糖代谢改变以及葡萄糖需求增加。因此,靶向葡萄糖摄取和代谢可能为发现区分正常细胞和恶性细胞的化合物带来新机会。本综述讨论了通过易化葡萄糖转运蛋白(GLUTs)开发新型葡萄糖摄取抑制剂的不同化学方法,并重点介绍了迄今为止已知的最先进和最有效的抑制剂类别。GLUT抑制剂不仅可能应用于癌症治疗,还可能应用于其他表现出葡萄糖成瘾的增殖性疾病的治疗。