Browse wiki

Jump to: navigation, search
Bastos Sant'Anna Silva 2018 Life Sciences Meeting 2018 Innsbruck AT
Coupling states ROUTINE  +
Diseases Cancer  +
Enzyme Complex II;succinate dehydrogenase  +
Event Oral  +
Has abstract Succinate is a substrate mainly metabolize
Succinate is a substrate mainly metabolized to fumarate in mitochondria by succinate dehydrogenase (SDH) or Complex II. SDH is located at the inner mitochondrial membrane, coupling the oxidation of succinate to fumarate in the tricarboxylic acid cycle (TCA) with electron transfer to ubiquinone. Inhibition or downregulation of SDH leads to an impairment of TCA cycle and respiratory activity, and consequently to accumulation of succinate. This, in turn, transmits an oncogenic signal from mitochondria to the cytosol. Cytosolic succinate inhibits the hypoxia inducible factor 1α (HIF1α) prolyl hydroxylase (PHD) leading to HIF1α stabilization. In this “pseudohypoxic” state angiogenesis and anaerobic metabolism are enhanced, ultimately leading to tumour progression. While succinate has essential implications on prostate cancer development, it is difficult to control intracellular succinate concentrations in intact cells due to the low permeability of plasma membranes to the compound. To overcome this limitation, we applied novel plasma membrane-permeable succinate (NV118) and malonate (inhibitor of SDH, NV161) prodrugs in high-resolution respirometry (Oroboros O2k-FluoRespirometer). Mitochondrial respiration was assessed in three cell lines: RWPE-1 (prostate; noncancerous), LNCaP (prostate; cancer), and HEK293T (embryonic kidney; control). NV118 (250 µM) stimulated ROUTINE respiration in LNCaP cancer cells by 18% as compared to vehicle (DMSO), while respiration remained unchanged in RWPE-1 (4% increase) and HEK 293T cells, even at higher concentrations of the prodrug. NV161 (66 µM) had no effect on ROUTINE respiration of HEK 293T cells. Our results indicate enhanced utilization of external, plasma membrane-permeable succinate in mitochondrial respiration in LNCaP prostate cancer cells but not in control cell lines. The cell-permeable prodrugs offer promising research tools to elucidate the roles of succinate and inhibition of SDH in metabolic reprograming towards a malignant phenotype.
eprograming towards a malignant phenotype.  +
Has editor [[Sant'Anna-Silva ACB]]  + , [[Kandolf G]]  +
Has publicationkeywords mitochondrial respiration  + , intact cells  + , cell-permeable succinate  +
Has title Effect of cell-permeable succinate and malonate prodrugs on mitochondrial respiration in prostate cancer cells.  +
Instrument and method Oxygraph-2k  +
MiP area Respiration  + , Pharmacology;toxicology  +
Preparation Permeabilized cells  + , Intact cells  +
Respiration and regulation Calcium  + , Substrate  +
Tissue and cell Kidney  + , Other cell lines  + , HEK  +
Was published by MiPNetLab AT Innsbruck Gnaiger E + , AT Innsbruck Oroboros + , SE Lund Elmer E +
Was submitted in year 2018  +
Was submitted to event Life Sciences Meeting 2018 Innsbruck AT +
Was written by Bastos Sant'Anna Silva AC + , Elmer E + , Meszaros A + , Gnaiger E +
Categories Abstracts
Modification date
"Modification date" is a predefined property that corresponds to the date of the last modification of a subject and is provided by Semantic MediaWiki.
13:40:21, 27 March 2019  +
hide properties that link here 
Sant'Anna-Silva 2018 Life Sciences Meeting 2018 Innsbruck AT + redirect page
 
Enter the name of the page to start browsing from.