Greif Charles E, Mertens R Tyler, Berger Gilles, Parkin Sean, Awuah Samuel G
Department of Chemistry, University of Kentucky Lexington Kentucky 40506 USA
Harvey Cushing Neuro-Oncology Laboratories, Department of Neurosurgery, Brigham and Women's Hospital, Harvard Medical School Boston MA 02115 USA.
RSC Chem Biol. 2023 May 25;4(8):592-599. doi: 10.1039/d3cb00051f. eCollection 2023 Aug 3.
Glioblastoma multiforme (GBM) is the most lethal brain cancer subtype, often advanced by the time of initial diagnosis. Existing treatment modalities including surgery, chemotherapy and radiation have been stymied by recurrence, metastasis, drug resistance and brain targetability. Here, we report a geometrically distinct Au(i) complex ligated by N^N-bidentate ligands and supported by a N-heterocyclic ligand that modulates mitochondrial morphology to inhibit GBM and . This work benefits from the facile preparation of anti-GBM Au(i)-NHC complexes.
多形性胶质母细胞瘤(GBM)是最致命的脑癌亚型,在初次诊断时通常已处于晚期。包括手术、化疗和放疗在内的现有治疗方式一直受到复发、转移、耐药性和脑靶向性的阻碍。在此,我们报告了一种几何结构独特的金(I)配合物,它由N^N双齿配体连接,并由一个N-杂环配体支撑,该配体可调节线粒体形态以抑制GBM 。这项工作得益于抗GBM金(I)-氮杂环卡宾配合物的简便制备。