Source:http://linkedlifedata.com/resource/pubmed/id/17036199
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2006-11-6
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pubmed:abstractText |
Photodynamic therapy (PDT) is a cancer treatment based on the interaction of a photosensitizer, light and oxygen. PDT with the endogenous photosensitizer, protoporphyrin IX (PpIX) induced by 5-aminolevulinic acid (ALA) or its derivatives is a modification of this treatment modality with successful application in dermatology. However, the mechanism of cell destruction by ALA-PDT has not been elucidated. In this study a human T-cell lymphoma Jurkat cell line was treated with PDT using hexaminolevulinate (HAL, hexylester of ALA). Four hours following treatment nearly 80% of the cells exhibited typical apoptotic features. Mitochondrial pro-apoptotic proteins were evaluated by Western blots in subcellular fractionated samples. PDT caused cytosolic translocation of cytochrome c and nuclear redistribution of apoptosis-inducing factor (AIF), but the release of mitochondrial Smac/DIABLO, Omi/HtrA2 and EndoG was not observed. The release of cytochrome c was followed by the cleavage of caspase-9 and caspase-3 as well as its downstream substrates, together with oligonucleosomal DNA fragmentation. The pan-caspases inhibitor, z-VAD.fmk, prevented oligonucleosomal DNA fragmentation, but failed to inhibit PDT-mediated apoptosis. The apoptotic induction by AIF-mediated caspase-independent pathway was also found after HAL-PDT with large-scale DNA fragmentation in the presence of z-VAD.fmk. These results demonstrate that cytochrome c-mediated caspase-dependent pathway and AIF-induced caspase-independent pathway are simultaneously involved in the apoptotic induction by PDT. When the cytochrome c-induced caspase-dependent pathway is blocked, the cells go into apoptosis via AIF-mediated pathway, clearly demonstrating that the cytochrome c-mediated caspase-dependent pathway is not required for such apoptotic induction. This finding may have an impact on improved PDT effectiveness.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/5-aminolevulinic acid hexyl ester,
http://linkedlifedata.com/resource/pubmed/chemical/AIFM1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Amino Acid Chloromethyl Ketones,
http://linkedlifedata.com/resource/pubmed/chemical/Aminolevulinic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Apoptosis Inducing Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Caspases,
http://linkedlifedata.com/resource/pubmed/chemical/Cytochromes c,
http://linkedlifedata.com/resource/pubmed/chemical/Enzyme Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Protoporphyrins,
http://linkedlifedata.com/resource/pubmed/chemical/benzyloxycarbonylvalyl-alanyl-aspart...,
http://linkedlifedata.com/resource/pubmed/chemical/protoporphyrin IX
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1360-8185
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2031-42
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pubmed:meshHeading |
pubmed-meshheading:17036199-Amino Acid Chloromethyl Ketones,
pubmed-meshheading:17036199-Aminolevulinic Acid,
pubmed-meshheading:17036199-Apoptosis,
pubmed-meshheading:17036199-Apoptosis Inducing Factor,
pubmed-meshheading:17036199-Caspases,
pubmed-meshheading:17036199-Cytochromes c,
pubmed-meshheading:17036199-Enzyme Inhibitors,
pubmed-meshheading:17036199-Humans,
pubmed-meshheading:17036199-Jurkat Cells,
pubmed-meshheading:17036199-Leukemia, T-Cell,
pubmed-meshheading:17036199-Membrane Potential, Mitochondrial,
pubmed-meshheading:17036199-Mitochondria,
pubmed-meshheading:17036199-Photochemotherapy,
pubmed-meshheading:17036199-Protoporphyrins
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pubmed:year |
2006
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pubmed:articleTitle |
Involvement of both caspase-dependent and -independent pathways in apoptotic induction by hexaminolevulinate-mediated photodynamic therapy in human lymphoma cells.
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pubmed:affiliation |
Pathology Clinic, Rikshospitalet-Radiumhospitalet HF Medical Center, Faculty Division Radiumhospitalet, University of Oslo, Norway.
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pubmed:publicationType |
Journal Article
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