Title of article :
Vitamin D sensitizes breast cancer cells to the action of H2O2: Mitochondria as a convergence point in the death pathway
Author/Authors :
Gregory E. Weitsman، نويسنده , , Ruth Koren، نويسنده , , Efrat Zuck، نويسنده , , Carmela Rotem، نويسنده , , Uri A. Liberman، نويسنده , , Amiram Ravid، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
13
From page :
266
To page :
278
Abstract :
Calcitriol, the hormonal form of vitamin D3, sensitizes breast cancer cells to reactive oxygen species (ROS)-dependent cytotoxicity induced by various anticancer modalities. This effect could be due to increased generation of ROS and/ or to increased sensitivity of the target cells to ROS. This work examined the effect of calcitriol on the damage inflicted on breast cancer cells by the direct action of ROS represented by H2O2. Treatment of MCF-7 cells with H2O2 resulted in activation of caspase 7 as well as induction of caspase-independent cell death. Both were enhanced by 48–72 h of pretreatment with calcitriol. This effect was not due to modulation of H2O2 degradation or to a specific effect on OH-mediated cytotoxicity. The H2O2-induced drop in mitochondrial membrane potential and release of cytochrome c were enhanced by calcitriol. These findings indicate that calcitriol sensitizes breast cancer cells to ROS-induced death by affecting event(s) common to both caspase-dependent and -independent modes of cell death upstream to mitochondrial damage.
Keywords :
calcitriol , programmed cell death , caspase , mitochondria , Mitochondrial membrane potential , oxidative stress
Journal title :
Free Radical Biology and Medicine
Serial Year :
2005
Journal title :
Free Radical Biology and Medicine
Record number :
520242
Link To Document :
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