Source:http://linkedlifedata.com/resource/pubmed/id/12827307
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
|
pubmed:dateCreated |
2003-10-2
|
pubmed:abstractText |
L-ascorbic acid (vitamin C) has been reported to play a role in the treatment and prevention of cancer. However, its specific mechanistic pathways remain obscure. This study was carried out to identify the sodium ascorbate-induced apoptotic pathway in B16F10 murine melanoma cells. Sodium ascorbate was found to induce the apoptosis of B16F10 murine melanoma in a time- and dose-dependent manner, and this was prevented by pretreatment with N-acetyl- L-cysteine (NAC), a well-known antioxidant. In fact, sodium ascorbate-treated B16F10 melanoma cells showed increased intracellular reactive oxygen species generation (ROS) levels. These results indicate that sodium ascorbate induced apoptosis in B16F10 murine melanoma cells by acting as a prooxidant. We examined the involvement of caspase-8 using a specific caspase-8 inhibitor (z-IETD-fmk) on the sodium ascorbate-induced apoptotic pathway. Cell death was found not to be inhibited by z-IETD-fmk treatment, indicating that sodium ascorbate-induced apoptosis is not mediated by caspase-8. In addition, we detected a reduction in the mitochondrial membrane potential during apoptosis and confirmed cytochrome-c release from mitochondria by immunoblotting. Taken together, it appears that the induction of a prooxidant state by sodium ascorbate and a subsequent reduction in mitochondrial membrane potential are involved in the apoptotic pathway of B16F10 murine melanoma cells, and that this occurs in a caspase-8-independent manner.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Casp8 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Casp9 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 8,
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 9,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochromes c,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidants,
http://linkedlifedata.com/resource/pubmed/chemical/Reactive Oxygen Species
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0340-7004
|
pubmed:author |
pubmed-author:BangSaicS,
pubmed-author:ChoDaehoD,
pubmed-author:HahmEunsilE,
pubmed-author:HurDaeyoungD,
pubmed-author:HwangYoung IlYI,
pubmed-author:KangJae SeungJS,
pubmed-author:KimDaejinD,
pubmed-author:KimYoung-InYI,
pubmed-author:LeeWang JaeWJ,
pubmed-author:ParkHyunjeongH,
pubmed-author:YangYoolheeY
|
pubmed:issnType |
Print
|
pubmed:volume |
52
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
693-8
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:12827307-Animals,
pubmed-meshheading:12827307-Apoptosis,
pubmed-meshheading:12827307-Ascorbic Acid,
pubmed-meshheading:12827307-Caspase 8,
pubmed-meshheading:12827307-Caspase 9,
pubmed-meshheading:12827307-Caspases,
pubmed-meshheading:12827307-Cytochromes c,
pubmed-meshheading:12827307-Dose-Response Relationship, Drug,
pubmed-meshheading:12827307-Melanoma, Experimental,
pubmed-meshheading:12827307-Membrane Potentials,
pubmed-meshheading:12827307-Mice,
pubmed-meshheading:12827307-Mitochondria,
pubmed-meshheading:12827307-Oxidants,
pubmed-meshheading:12827307-Reactive Oxygen Species,
pubmed-meshheading:12827307-Tumor Cells, Cultured
|
pubmed:year |
2003
|
pubmed:articleTitle |
L-ascorbic acid (vitamin C) induces the apoptosis of B16 murine melanoma cells via a caspase-8-independent pathway.
|
pubmed:affiliation |
Department of Anatomy and Tumor Immunity Medical Research Center, Seoul National University College of Medicine, 110-799 Seoul, South Korea.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|