Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P33527 (
ABCC1
)
1,164
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Even though the BCR-ABL tyrosine kinase inhibitor imatinib significantly improves the prognosis of chronic myelogenous leukaemia (CML) patients, drug resistance is a major obstacle to better management. We examined the interaction of recently defined bone marrow microenvironment factors
CXCL12
and ATP-binding cassette (ABC) transporters in the bone marrow of CML patients in the chronic phase and blast crisis.Expression levels of mRNA extracted from frozen specimens of CML patients were measured by real-time polymerase chain reaction. The expression of the ABC transporters MDR1,
ABCC1
, ABCG2, and
CXCL12
was significantly higher in the bone marrow samples of CML blast crisis than in those of CML chronic phase. Immunohistochemical staining for
CXCL12
revealed that the proportion of
CXCL12
positive reticular cell areas correlated well with the mRNA levels of
CXCL12
in CML bone marrow. Finally, co-culture experiments of K562 CML cells with
CXCL12
expressing mesenchymal cells (OP9 cells or human
CXCL12
transfected 3T3 cells) revealed enhanced mRNA levels for MDR1 in a
CXCL12
rich environment.These results suggest that imatinib treatment restores the bone marrow microenvironment in CML with the presence of
CXCL12
expressing reticular cells but in turn induces the overexpression of MDR1 in haematopoietic cells due to up-regulated expression of
CXCL12
.
...
PMID:Expression of multidrug resistance 1 gene in association with CXCL12 in chronic myelogenous leukaemia. 2539 53