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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1987-8-13
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pubmed:abstractText |
Changes in the concentration of intracellular Ca2+ may be an important component of the mechanism of adriamycin toxicity to tumor cells. Adriamycin interacts with the plasma membrane, a phenomenon which may lead to a direct modulation of Ca2+ transport proteins or, since the drug is a quinone, may lead to indirect changes in Ca2+ homeostasis induced by oxidative stress to the cell. The calcium content of L1210 murine leukemia cells treated with adriamycin for up to 6 hr was estimated using the cell-impermeant dye arsenazo-III. Pools of intracellular Ca2+ were released to the extracellular compartment, where they reacted with the dye by sequential treatment of the cells with m-fluorocarbonylcyanidediphenylhydrazone (FCCP) and the Ca2+-ionophore A23187. Pretreatment of L1210 cells with ruthenium red (5 microM) selectively decreased the FCCP-releasable Ca2+ pool, which suggested it was mitochondrial in origin. Continuous exposure of L1210 murine leukemia cells in vitro to 5 or 10 microM adriamycin for 2 hr did not produce any change in the intracellular concentration of releasable Ca2+; at 4 hr, however, the total releasable pool of Ca2+ rose by 29% and 46% for 5 and 10 microM adriamycin respectively. This increase was seen predominantly in the mitochondrial pool. Exposure of L1210 cells to the quinone, menadione, also increased the releasable pools of cellular Ca2+ but like adriamycin, only after an incubation period of 4 hr. These results contrasted with a rapid decrease in mitochondrial Ca2+ concentration produced by a short (5 min) exposure to 500 microM t-butylhydroperoxide, a generator of free radicals. After treatment with 8 mM lidocaine, a membrane fluidizing agent, there was a rapid fall in extramitochondrial Ca2+. These findings suggest that changes in L1210 Ca2+ homeostasis induced by adriamycin and menadione are late, and possibly common, events of quinone toxicity to L1210 cells, adriamycin does not have an immediate effect on Ca2+ ion transport produced by the direct interaction of the antibiotic with the plasma membrane, and oxidative stress induced by redox-active quinones may not be important for the induction of toxicity in neoplastic cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Doxorubicin,
http://linkedlifedata.com/resource/pubmed/chemical/Lidocaine,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases,
http://linkedlifedata.com/resource/pubmed/chemical/Peroxides,
http://linkedlifedata.com/resource/pubmed/chemical/Ruthenium Red,
http://linkedlifedata.com/resource/pubmed/chemical/Vitamin K,
http://linkedlifedata.com/resource/pubmed/chemical/tert-Butylhydroperoxide
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0277-5379
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
23
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
295-302
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2439346-Animals,
pubmed-meshheading:2439346-Calcium,
pubmed-meshheading:2439346-Doxorubicin,
pubmed-meshheading:2439346-Intracellular Fluid,
pubmed-meshheading:2439346-Leukemia L1210,
pubmed-meshheading:2439346-Lidocaine,
pubmed-meshheading:2439346-Mice,
pubmed-meshheading:2439346-Oxidoreductases,
pubmed-meshheading:2439346-Peroxides,
pubmed-meshheading:2439346-Ruthenium Red,
pubmed-meshheading:2439346-Vitamin K,
pubmed-meshheading:2439346-tert-Butylhydroperoxide
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pubmed:year |
1987
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pubmed:articleTitle |
The effects of adriamycin on intracellular calcium concentrations of L1210 murine leukemia cells.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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