Vitamin D3 attenuates doxorubicin-induced senescence of human aortic endothelial cells by upregulation of IL-10 via the pAMPKα/Sirt1/Foxo3a signaling pathway
Keyword(s):
The toxicity of doxorubicin to the cardiovascular system often limits its benefits and widespread use as chemotherapy. The mechanisms involved in doxorubicin-induced cardiovascular damage and possible protective interventions are not well-explored. Using human aortic endothelial cells, we show vitamin D3 strongly attenuates doxorubicin-induced senescence and cell cycle arrest. We further show the protective effects of vitamin D3 are mediated by the upregulation of IL-10 and FOXO3a expression through fine modulation of pAMPKα/SIRT1/FOXO3a complex activity. These results have great significance in finding a target for mitigating doxorubicin-induced cardiovascular toxicity.
2014 ◽
Vol 2014
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pp. 1-9
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2015 ◽
Vol 241
(1)
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pp. e6
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Infection with a periodontal pathogen induces procoagulant effects in human aortic endothelial cells
2006 ◽
Vol 4
(10)
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pp. 2256-2261
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2005 ◽
Vol 73
(12)
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pp. 8050-8059
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