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ABSTRACT: Background
The mechanism behind poor survival of acute myeloid leukemia (AML) patients with 1-barabinofuranosylcytosine (Ara-C) based treatment remains unclear. This study aimed to assess the pharmacogenomic effects of Ara-C metabolic pathway in patients with AML.Methods
The genotypes of 19 single nucleotide polymorphisms (SNPs) of DCK, CDA and SLC29A1from 100 AML patients treated with Ara-C were examined. All the SNPs were screened with ligase detection reaction assay. The transcription analysis of genes was examined by quantitative real time polymerase chain reaction. The association between clinical outcome and gene variants was evaluated by Kaplan-Meier method.Results
Genotypes of rs9394992 and rs324148 for SLC29A1 in remission patients were significantly differ
SUBMITTER: Wan H
PROVIDER: S-EPMC4234887 | biostudies-literature | 2014 Nov
REPOSITORIES: biostudies-literature