Source:http://linkedlifedata.com/resource/pubmed/id/10897619
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
46
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pubmed:dateCreated |
2000-8-22
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pubmed:abstractText |
MDR1 gene encodes for a transmembranous glycoprotein, gp-170, which acts as a drug export pump and is also a cyclosporine(CsA)-binding protein. This study aimed at evaluating MDR1 expression in NS sensitive(S) and resistant(R) to therapy (steroids/S/, cyclophosphamide/C/, CsA) patients. Twenty six boys, 13 girls aged 3-8 years were included to the study. MDR1 was analysed using: 1) evaluation of gp-170 activity according to DiC2/3/ [3,3-Diethyloxa-carbocyanine Iodide] by means of flow cytometry and as 2) mRNA expression of MDR1 determined by RT-PCR. The analysis was performed in the lymphocyte subset CD4/CD45RA presenting suppressor-inducer activity. Negative control, Jurkat-T-cell line, not expressing the MDR1 phenotype, was transfected with viral expression vector containing a full-length cDNA for the human MDR1 gene. We found that: in SR-NS the high expression of MDR1 was associated mainly with the suppressor-inducer T-cells (CD45RA+CD4+) and was subsequently enhanced during an ineffective treatment with C and/or CsA. C-R-NS and CsA-R-NS were partially reversible by S- and R-Verapamil; this was in vitro confirmed by inhibition of export pump activity, gp-170. SS-NS, C-S-NS and CsA-S-NS presented the low expression and activity of MDR1 comparing to R-children (p < 0.001) and healthy controls (p < 0.00001). Resistance to therapy in NS patients seems to be resulted from the enhanced expression of MDR1 gene and subsequent high activity of export pump P-gp-170. Calcium channel blockers may reverse the MRD1-related resistance in the therapy of NS. Analysis of MDR1 may help to detect of suspected therapy resistance in NS.
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pubmed:language |
pol
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1426-9686
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pubmed:author |
pubmed-author:BaldamusC ACA,
pubmed-author:Hyla-KlekotLL,
pubmed-author:MaciejewskiJJ,
pubmed-author:Medy?skaAA,
pubmed-author:Musia?WW,
pubmed-author:PeszkoAA,
pubmed-author:Rogowska-KaliszAA,
pubmed-author:RunowskiDD,
pubmed-author:SieniawskaMM,
pubmed-author:StachowskiJJ,
pubmed-author:SzprygnerKK,
pubmed-author:WeglarskaJJ,
pubmed-author:ZaniewMM,
pubmed-author:ZankerC BCB,
pubmed-author:Zwoli?skaDD
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pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
218-21
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10897619-Anti-Inflammatory Agents,
pubmed-meshheading:10897619-Child,
pubmed-meshheading:10897619-Child, Preschool,
pubmed-meshheading:10897619-Cyclophosphamide,
pubmed-meshheading:10897619-Drug Resistance,
pubmed-meshheading:10897619-Female,
pubmed-meshheading:10897619-Genes, MDR,
pubmed-meshheading:10897619-Humans,
pubmed-meshheading:10897619-Immunosuppressive Agents,
pubmed-meshheading:10897619-Male,
pubmed-meshheading:10897619-Nephrotic Syndrome,
pubmed-meshheading:10897619-Steroids
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pubmed:year |
2000
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pubmed:articleTitle |
[Resistance to therapy in primary nephrotic syndrome: effect of MDR1 gene activity].
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pubmed:affiliation |
Kliniki Chorób Dzieci Akademii Medycznej w Poznaniu.
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pubmed:publicationType |
Journal Article,
English Abstract
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