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dc.contributor.authorWentzel, Johannes F.
dc.contributor.authorLewies, Angelique
dc.contributor.authorBronkhorst, Abel J.
dc.contributor.authorVan Dyk, Etresia
dc.contributor.authorDu Plessis, Lissinda H.
dc.contributor.authorPretorius, Piet J.
dc.date.accessioned2017-03-15T13:52:28Z
dc.date.available2017-03-15T13:52:28Z
dc.date.issued2017
dc.identifier.citationWentzel, J.F. et al. 2017. Exposure to high levels of fumarate and succinate leads to apoptotic cytotoxicity and altered global DNA methylation profiles in vitro. Biochimie, 135:28-34. [https://doi.org/10.1016/j.biochi.2017.01.004]en_US
dc.identifier.issn0300-9084
dc.identifier.issn1638-6183 (Online)
dc.identifier.urihttp://hdl.handle.net/10394/20841
dc.identifier.urihttps://doi.org/10.1016/j.biochi.2017.01.004
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0300908417300111
dc.description.abstractIn the Krebs cycle, succinate is oxidized to fumarate by succinate dehydrogenase (SDH), followed by the conversion of fumarate to malate by fumarate hydratase (FH). In cells with defective SDH and FH, the Krebs cycle is congested, respiration impaired and fumarate and succinate accumulates. Several studies have indicated that the accumulation of these substrates are associated with cytotoxicity and oncogenesis. High levels of succinate and fumarate induce hypoxia inducible factor (HIF1A) hydroxylases, leading to the activation of oncogenic HIF pathways. However, the role of HIF as primary inducer of oncogenic change has been questioned, as other non-enzymatic mechanisms have been shown to interfere with cellular metabolism, cell signalling as well as disrupting protein function. Owing to the essential roles that SDH and FH play in cellular energy metabolism, and their associated tumor suppressor capacity, it is vital to understand the biochemical effects resulting from the accumulation of their associated metabolites. Therefore, in this study, we investigated the effect of high concentrations of succinate and fumarate exposure on cell viability, genome integrity and global DNA methylation using a human hepatocellular carcinoma (HepG2) cell culture model. It was found that relatively high concentrations of succinate and fumarate cause a loss of cell viability, which seems to be orchestrated through an apoptotic pathway. Cells exposed to high levels of succinate also presented with elevated caspase 3 and/or caspase 7 levels. In addition, elevated levels of fumarate lead to extensive DNA fragmentation, which may contribute pathophysiologically by inducing chromosomal instability, while succinate demonstrated lower genotoxicity. Furthermore, both succinate and fumarate altered the global DNA methylation patterns via significant DNA hypermethylation. Since numerous studies have reported correlations between aberrant DNA methylation and oncogenesis, hypermethylation may contribute to the oncogenesis observed in cells exposed to high concentrations of these metabolitesen_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectSuccinateen_US
dc.subjectFumarateen_US
dc.subjectApoptosisen_US
dc.subjectDNA methylationen_US
dc.subjectMethylation sensitive comet assayen_US
dc.subjectCanceren_US
dc.titleExposure to high levels of fumarate and succinate leads to apoptotic cytotoxicity and altered global DNA methylation profiles in vitroen_US
dc.typeArticleen_US
dc.contributor.researchID20577966 - Lewies, Angelique
dc.contributor.researchID22195289 - Bronkhorst, Abel Jacobus
dc.contributor.researchID12126497 - Van Dyk, Etresia
dc.contributor.researchID11948388 - Du Plessis, Lissinda Hester
dc.contributor.researchID10176705 - Pretorius, Petrus Jacobus
dc.contributor.researchID20134045 - Wentzel, Johannes Frederik


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