NT5C3 polymorphisms and outcome of first induction chemotherapy in acute myeloid leukemia.

PHARMACOGENETICS AND GENOMICS(2014)

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摘要
Aims The cytosolic 5'-nucleotidase-III (NT5C3) is involved in the metabolism of the nucleoside analog, cytosine arabinose (AraC), and the expression level of NT5C3 is correlated with sensitivity to AraC in acute myeloid leukemia (AML) patients. The current study examined whether the NT5C3 polymorphisms could affect chemotherapy outcomes in 103 Korean AML patients. Methods Forty-seven single nucleotide polymorphisms in NT5C3 were genotyped using the Illumina GoldenGate genotyping assay. The genetic effects of the polymorphisms on the outcome of chemotherapy were analyzed using chi(2) and logistic regression models. Results Although none of the NT5C3 polymorphisms was associated with a complete remission rate, a common single nucleotide polymorphism, rs3750117, showed a significant association with induction rate after the first course of chemotherapy (P-corr=0.004 and odds ratio = 11.28) in AML patients. In addition, NT5C3 expression levels were significantly increased in patients with risk allele homozygote. Conclusions The data suggest that genotyping the NT5C3 polymorphism may have the potential to identify patients more likely to respond to AraC-based chemotherapy. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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acute myeloid leukemia,chemotherapy,cytosine arabinose,NT5C3,single nucleotide polymorphism
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