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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >ABCB1 genetic variation and P-glycoprotein expression/activity in a cohort of Brazilian acute myeloid leukemia patients.
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ABCB1 genetic variation and P-glycoprotein expression/activity in a cohort of Brazilian acute myeloid leukemia patients.

机译:巴西急性髓细胞性白血病患者队列中的ABCB1遗传变异和P-糖蛋白表达/活性。

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摘要

Polymorphisms in the ABCB1 gene may influence P-glycoprotein (Pgp) expression and/or activity. Because the population in Brazil is markedly heterogeneous, we analyzed the relationship between ABCB1 polymorphisms and Pgp expression/activity in Brazilian acute myeloid leukemia (AML) patients.Acute myeloid leukemia samples from 109 patients were studied. ABCB1 gene variants rs1128503 (C1236T) and rs1045643 (C3435T) were analyzed by PCR-RFLP assay. Pgp expression and Pgp activity were analyzed by flow cytometry.There was a similar distribution of Pgp expression and activity on polymorphisms C1236T, C1236C, and T1236T for exon 12, and C3435T, C3435C, and T3435T for exon 26. An exception was observed in the lowest ratio of mean fluorescence intensity (MFI) median for Pgp expression in the TT genotype for both studied exons, and its correspondence to a low MFI median for Pgp activity. Pgp expression did not show impact on the response to remission induction therapy, but the MFI median of Pgp expression in the remission failure group was higher than that of the complete remission (CR) group of patients (p = 0.04). Overall survival (OS) was significantly influenced by CR (p = 0.0001). Better 5-year OS and 5-year event-free survival rates (p = 0.04 and p = 0.007, respectively) were achieved in patients presenting the genetic variant CC in exon 12 followed by those presenting the variant CT in exon 26 (p = 0.001).Polymorphisms in the ABCB1 gene and the levels of Pgp expression could be useful to identify prognostic in AML patients.
机译:ABCB1基因中的多态性可能会影响P-糖蛋白(Pgp)的表达和/或活性。由于巴西人口明显异质,我们分析了巴西急性髓细胞性白血病(AML)患者的ABCB1多态性与Pgp表达/活性之间的关系。研究了109例急性髓性白血病患者的样本。通过PCR-RFLP分析分析了ABCB1基因变体rs1128503(C1236T)和rs1045643(C3435T)。通过流式细胞术分析Pgp表达和Pgp活性。外显子12的C1236T,C1236C和T1236T多态性以及外显子26的C3435T,C3435C和T3435T多态性的Pgp表达和活性分布相似。对于两个研究的外显子,TT基因型中Pgp表达的平均荧光强度(MFI)中位数的最低比率,与低PFI活动的MFI中位数相对应。 Pgp表达未显示对缓解诱导疗法的反应有影响,但是缓解失败组中Pgp表达的MFI中位数高于完全缓解(CR)组的患者(p = 0.04)。 CR显着影响了总生存期(p = 0.0001)。在外显子12中出现遗传变异CC的患者,在外显子26中出现变异CT的患者,获得了更好的5年OS和5年无事件生存率(分别为p = 0.04和p = 0.007)(p = 0.001).ABCB1基因的多态性和Pgp表达水平可能有助于确定AML患者的预后。

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