Polymorphisms in multidrug resistance-associated protein gene 4 is associated with outcome in childhood acute lymphoblastic leukemia

被引:77
作者
Ansari, Marc [1 ,2 ]
Sauty, Geraldine [1 ]
Labuda, Malgorzata [1 ]
Gagne, Vincent [1 ]
Laverdiere, Caroline [1 ,3 ]
Moghrabi, Albert [1 ,3 ]
Sinnett, Daniel [1 ,3 ]
Krajinovic, Maja [1 ,3 ,4 ]
机构
[1] CHU St Justine, Ctr Rech, Montreal, PQ H3T 1C5, Canada
[2] Univ Hosp Geneva, Dept Pediat, Geneva, Switzerland
[3] Univ Montreal, Dept Pediat, Montreal, PQ H3C 3J7, Canada
[4] Univ Montreal, Dept Pharmacol, Montreal, PQ H3C 3J7, Canada
关键词
PHARMACOGENOMICS; TRANSPORTERS; EXPRESSION; METHOTREXATE; VARIANTS; ABCC4; MRP4;
D O I
10.1182/blood-2008-11-191098
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Methotrexate and 6-mercaptopurine, important components of acute lymphoblastic leukemia treatment, are substrates for multidrug resistance-associated protein MRP4. Eight single nucleotide polymorphisms were analyzed in MRP4 gene, and 4 variants were identified as tagSNPs with frequency more than or equal to 5%. They were investigated for association with treatment responses in 275 children with acute lymphoblastic leukemia. The TC genotype of the regulatory T-1393C polymorphism was associated with better event-free survival (P =.02) and lower methotrexate plasma levels (P = .01). The CA genotype of A934C (Lys304Asn) substitution correlated in contrast with lower event-free survival (P = .02) and higher frequency of high-grade thrombocytopenia (P = .01). Gene reporter assay showed that the promoter haplotype uniquely tagged by the C-1393 allele conferred higher promoter activity compared with remaining haplotypes (P < .001). Further analyses are needed to replicate this pilot study and get closer insight into the functional effect of these polymorphisms. (Blood. 2009;114:1383-1386)
引用
收藏
页码:1383 / 1386
页数:4
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