Source:http://linkedlifedata.com/resource/pubmed/id/20723297
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2010-8-20
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pubmed:abstractText |
This study was purposed to investigate the relationship between activation of nuclear factor-?B (NF-?B) and multidrug resistance in K562/AO? cells and its mechanism. Human erythroleukemic cell line K562 and its adriamycin-resistant counterpart K562/AO? cells were used in the study. After inhibiting the activation of NF-?B with noncytotoxic concentration of antioxidant pyrrolidine dithiocarbamate (PDTC) in vitro, the multiple of drug resistance of K562/AO? cells was assessed by MTT assay. RT-PCR and flow cytometry method were used to detect the relative expression of mdr-1 mRNA and P-gp, respectively. The results showed that (1) multidrug resistance of K562/AO? cells to ADM was 59 times higher than that of K562 cells. When being pretreated with 0.2 ?mol/L PDTC which is noncytotoxic to cells, the IC?? of ADM in K562/AO? cells was sharply decreased with relative reverse efficiency of 93.03%, which was more higher than that of classic modifying agents Verapamil (Ver); (2) NF-?B activity of K562/AO? cells was significantly higher than that of K562 cells (p < 0.01). When being treated with PDTC, the activation of NF-?B was sharply decreased in K562/AO? cells; with 0.2 ?mol/L PDTC for 24 hours it decreased to the lowest, nearly to the K562 cell level (p > 0.05); (3) the relative expression of both mdr-1 mRNA and P-gp in K562/AO? cells was more higher; the expressions of mdr-1 mRNA and P-gp both were inhibited in K562/AO? cell group treated with PDTC for 48 hours. It is concluded that the PDTC used as an inhibitor of NF-?B activity can partially reverse the multidrug resistance of K562/AO? cells, which mechanism can be associated with the down-regulation of mdr-1 mRNA and P-gp.
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pubmed:language |
chi
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/ABCB1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa B,
http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoprotein,
http://linkedlifedata.com/resource/pubmed/chemical/Protease Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrrolidines,
http://linkedlifedata.com/resource/pubmed/chemical/Thiocarbamates,
http://linkedlifedata.com/resource/pubmed/chemical/pyrrolidine dithiocarbamic acid
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1009-2137
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
903-8
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pubmed:meshHeading |
pubmed-meshheading:20723297-Drug Resistance, Multiple,
pubmed-meshheading:20723297-Drug Resistance, Neoplasm,
pubmed-meshheading:20723297-Humans,
pubmed-meshheading:20723297-K562 Cells,
pubmed-meshheading:20723297-NF-kappa B,
pubmed-meshheading:20723297-P-Glycoprotein,
pubmed-meshheading:20723297-Protease Inhibitors,
pubmed-meshheading:20723297-Pyrrolidines,
pubmed-meshheading:20723297-Thiocarbamates
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pubmed:year |
2010
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pubmed:articleTitle |
[Reversal effect of nuclear factor-?B protease inhibitor PDTC on multidrug resistance of K562/AO? cells and its mechanism].
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pubmed:affiliation |
Department of Pediatrics, Lianyungang Municipal Frist People Hospital, Lianyungang 222002, Jiangsu Province, China.
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pubmed:publicationType |
Journal Article,
English Abstract
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