An anti-glioblastoma gold(i)-NHC complex distorts mitochondrial morphology and bioenergetics to induce tumor growth inhibition.
Charles E GreifR Tyler MertensGilles BergerSean R ParkinSamuel G AwuahPublished in: RSC chemical biology (2023)
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 in vitro and in vivo . This work benefits from the facile preparation of anti-GBM Au(i)-NHC complexes.
Keyphrases
- reduced graphene oxide
- resting state
- oxidative stress
- white matter
- sensitive detection
- minimally invasive
- functional connectivity
- papillary thyroid
- cerebral ischemia
- quantum dots
- visible light
- squamous cell
- locally advanced
- radiation therapy
- free survival
- combination therapy
- molecularly imprinted
- high resolution
- young adults
- percutaneous coronary intervention