Department of Medicinal and Biological Chemistry, College of Pharmacy and Pharmaceutical Sciences, The University of Toledo, 2801, W. Bancroft Street, Toledo, Ohio 43606, United States.
Department of Biological Sciences, College of Natural Sciences and Mathematics, The University of Toledo, 2801, W. Bancroft Street, Toledo, Ohio 43606, United States.
J Med Chem. 2024 Sep 26;67(18):16107-16127. doi: 10.1021/acs.jmedchem.3c02084. Epub 2024 Sep 12.
Ferroptosis is a recently discovered cell death mechanism triggered by iron-dependent elevation of reactive oxygen species leading to lipid membrane peroxidation. We previously reported the development of a new class of ferroptosis inducers referred to as CETZOLEs with CC values in the low micromolar range. Structure-activity relationship study of these compounds led to the development of more potent analogs with CC values in the nanomolar range. Cells exposed to these compounds displayed the hallmarks of ferroptosis including cell death through ROS accumulation. Cancer cells were found to be more sensitive to these compounds than normal cells. Proteomic studies using covalent and affinity probes led to the identification of cystathionine β-synthase, peroxiredoxins, ADP/ATP carriers, and glucose dehydrogenase as enriched proteins. The binding of CETZOLEs to these proteins as well as GPX4 was validated by Western blotting. This group of proteins is known to be associated with cellular antioxidant pathways.
铁死亡是一种新发现的细胞死亡机制,由铁依赖性的活性氧(ROS)升高引发脂质膜过氧化。我们之前报道了一类新的铁死亡诱导剂,称为 CETZOLEs,其 CC 值在低微摩尔范围内。这些化合物的构效关系研究导致了 CC 值在纳摩尔范围内的更有效的类似物的发展。暴露于这些化合物的细胞表现出铁死亡的特征,包括通过 ROS 积累导致的细胞死亡。研究发现,癌细胞比正常细胞对这些化合物更为敏感。使用共价和亲和探针的蛋白质组学研究导致鉴定出半胱氨酸β-合酶、过氧化物酶、ADP/ATP 载体和葡萄糖脱氢酶为富集蛋白。CETZOLEs 与这些蛋白以及 GPX4 的结合通过 Western blot 得到了验证。这组蛋白已知与细胞抗氧化途径有关。