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Cyclosporin A potentiates the cytotoxic effects of methyl methanesulphonate in HL-60 and K562 cells
Mlejnek P, Frydrych I, Dolezel P.
Jazyk angličtina Země Velká Británie
- MeSH
- apoptóza účinky záření MeSH
- buňky K562 enzymologie patologie účinky léků MeSH
- cyklosporin toxicita MeSH
- DNA nádorová účinky léků MeSH
- financování organizované MeSH
- glutathion metabolismus MeSH
- glutathiondisulfid metabolismus MeSH
- HL-60 buňky enzymologie patologie účinky léků MeSH
- imunosupresiva toxicita MeSH
- kaspasa 3 biosyntéza MeSH
- lidé MeSH
- messenger RNA metabolismus MeSH
- methylmethansulfonát toxicita MeSH
- nekróza chemicky indukované MeSH
- oxidační stres účinky záření MeSH
- P-glykoprotein genetika metabolismus MeSH
- poškození DNA MeSH
- RNA nádorová analýza MeSH
- synergismus léků MeSH
- viabilita buněk účinky léků MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Check Tag
- lidé MeSH
Methyl methanesulphonate (MMS) is a DNA damaging agent, which induces oxidative stress, ATP depletion, and consequently, cell death, in HL-60 and K562 cells. The cell death induced by MMS predominantly exhibited the morphological and biochemical hallmarks of necrosis. A minor population of dying cells exhibited apoptotic hallmarks, especially in K562 cell cultures. Cyclosporin A (CsA) was used to modulate the MMS-induced cell death. Our results indicated that CsA did not prevent cells from dying, but changed the mode of death from necrotic to apoptotic. Surprisingly, CsA enhanced oxidative stress and increased the overall number of dead cells. Based on these results, we conclude that the modulatory effect of CsA on MMS-induced cell death might arise from an interference by CsA with mitochondrial metabolism, rather than from inhibition of the MMS efflux mediated by P-glycoprotein.
Citace poskytuje Crossref.org
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- $a Methyl methanesulphonate (MMS) is a DNA damaging agent, which induces oxidative stress, ATP depletion, and consequently, cell death, in HL-60 and K562 cells. The cell death induced by MMS predominantly exhibited the morphological and biochemical hallmarks of necrosis. A minor population of dying cells exhibited apoptotic hallmarks, especially in K562 cell cultures. Cyclosporin A (CsA) was used to modulate the MMS-induced cell death. Our results indicated that CsA did not prevent cells from dying, but changed the mode of death from necrotic to apoptotic. Surprisingly, CsA enhanced oxidative stress and increased the overall number of dead cells. Based on these results, we conclude that the modulatory effect of CsA on MMS-induced cell death might arise from an interference by CsA with mitochondrial metabolism, rather than from inhibition of the MMS efflux mediated by P-glycoprotein.
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