pubmed-article:10955805 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C0080103 | lld:lifeskim |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C0023467 | lld:lifeskim |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C0242643 | lld:lifeskim |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C0069906 | lld:lifeskim |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C0085415 | lld:lifeskim |
pubmed-article:10955805 | lifeskim:mentions | umls-concept:C1537044 | lld:lifeskim |
pubmed-article:10955805 | pubmed:issue | 8 | lld:pubmed |
pubmed-article:10955805 | pubmed:dateCreated | 2000-11-27 | lld:pubmed |
pubmed-article:10955805 | pubmed:abstractText | Despite treatment with intensive chemotherapy, a considerable number of patients with acute myeloid leukemia (AML) die from their disease due to the occurrence of resistance. Overexpression of the transporter proteins P-glycoprotein (P-gp) and multidrug resistance protein (MRP) 1 has been identified as a major cause of cross-resistance to functionally and structurally unrelated drugs. In the present study, the functional activity of P-gp and MRP was determined in 104 de novo AML patients with a flow cytometric assay using rhodamine 123 (Rh123) in combination with PSC833 and carboxyfluorescein (CF) in combination with MK-571. The results were compared with clinical outcome and with known prognostic factors. The functional activity of P-gp and MRP, expressed as Rh123 efflux blocking by PSC833 and CF efflux blocking by MK-571, demonstrated a great variability in the AML patients. A strong negative correlation was observed between Rh123 efflux blocking by PSC833 and Rh123 accumulation (r(s) = -0.69, P < 0.001) and between CF efflux blocking by MK-571 and CF accumulation (r(s) = -0.59, P < 0.001). A low Rh123 accumulation and a high Rh123 efflux blocking by PSC833 were associated with a low complete remission (CR) rate after the first cycle of chemotherapy (P = 0.008 and P = 0.01, respectively). Patients with both low Rh123 and CF accumulation (n = 16) had the lowest CR rate (6%), whereas patients with both high Rh123 and CF accumulation (n = 11) had a CR rate of 73%. AML patients with French-American-British classification M1 or M2 showed a lower Rh123 accumulation than patients with French-American-British classification M4 or M5 (P = 0.02). No association was observed between the multidrug resistance parameters and overall survival of the AML patients. Risk group was the only predictive parameter for overall survival (P = 0.003). | lld:pubmed |
pubmed-article:10955805 | pubmed:language | eng | lld:pubmed |
pubmed-article:10955805 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:10955805 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:10955805 | pubmed:month | Aug | lld:pubmed |
pubmed-article:10955805 | pubmed:issn | 1078-0432 | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:VellengaEE | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:VerhoefG EGE | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:OssenkoppeleG... | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:de VriesE GEG | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:VerdonckL FLF | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:van PuttenW... | lld:pubmed |
pubmed-article:10955805 | pubmed:author | pubmed-author:van der... | lld:pubmed |
pubmed-article:10955805 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:10955805 | pubmed:volume | 6 | lld:pubmed |
pubmed-article:10955805 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:10955805 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:10955805 | pubmed:pagination | 3205-14 | lld:pubmed |
pubmed-article:10955805 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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pubmed-article:10955805 | pubmed:year | 2000 | lld:pubmed |
pubmed-article:10955805 | pubmed:articleTitle | P-glycoprotein and multidrug resistance protein activities in relation to treatment outcome in acute myeloid leukemia. | lld:pubmed |
pubmed-article:10955805 | pubmed:affiliation | Department of Hematology, University Hospital Groningen, the Netherlands. | lld:pubmed |
pubmed-article:10955805 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10955805 | lld:pubmed |