| Literature DB >> 31654752 |
Sonia A Allen1, Sandipan Datta2, Jose Sandoval3, Alexey Tomilov4, Thomas Sears5, Kevin Woolard6, James M Angelastro7, Gino A Cortopassi8.
Abstract
AMP-activated protein kinase (AMPK) is a eukaryotic energy sensor and protector from mitochondrial/energetic stress that is also a therapeutic target for cancer and metabolic disease. Metformin is an AMPK inducer that has been used in cancer therapeutic trials. Through screening we isolated cetylpyridinium chloride (CPC), a drug known to dose-dependently inhibit mitochondrial complex 1, as a potent and dose-dependent AMPK stimulator. Mitochondrial biogenesis and bioenergetics changes have also been implicated in glioblastoma, which is the most aggressive form of brain tumors. Cetylpyridinium chloride has been administered in humans as a safe drug-disinfectant for several decades, and we report here that under in vitro conditions, cetylpyridinium chloride kills glioblastoma cells in a dose dependent manner at a higher efficacy compared to current standard of care drug, temozolomide.Entities:
Keywords: AMP-activated protein kinase; AMPK; Cancer; Cetylpyridinium chloride; Mitochondrial inhibitor; Quaternary ammonium salt
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Year: 2019 PMID: 31654752 DOI: 10.1016/j.mito.2019.09.009
Source DB: PubMed Journal: Mitochondrion ISSN: 1567-7249 Impact factor: 4.160