[No authors listed]
AIMS:Some members of the poly ADP-ribose polymerase protein family have been regarded as targets for the therapeutic inhibition of cancer. Among these genes, poly ADP-ribose polymerase family, member 15 is a candidate gene for cancer development due to its ability to regulate gene transcription and its reported association with apoptosis. The current study investigated the possible association between single-nucleotide polymorphisms and the risk of acute myeloid leukemia (AML). In addition, we analyzed the effects of the Pduanyu3715 polymorphisms on the clinical phenotypes associated with cytosine arabinose (AraC) chemotherapy in AML patients. METHODS:Ten Pduanyu3715 polymorphisms were genotyped via TaqMan assay in a total of 344 Korean subjects, including 103 AML patients and 241 normal controls. The genetic effects of the polymorphisms on the risk of AML and the clinical phenotypes were analyzed using Statistical Analysis System (SAS) software. RESULTS:The results from a Cox regression analysis for overall survival revealed that two polymorphisms were associated with increased overall survival and the signal for rs17208928 was retained after correcting for multiple tests (p(corr) < 0.05). CONCLUSIONS:These results suggest the possibility that the Pduanyu3715 gene may be a potential therapeutic target in AML patients although much larger scale studies are needed for validation.
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