Gézsi A, Lautner-Csorba O, Erdélyi D J, Hullám G, Antal P, Semsei Á F, Kutszegi N, Hegyi M, Csordás K, Kovács G, Szalai C
Department of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
Pharmacogenomics J. 2015 Jun;15(3):241-7. doi: 10.1038/tpj.2014.60. Epub 2014 Sep 30.
CYP3A4 has an important role in the metabolisms of many drugs used in acute lymphoblastic leukemia (ALL) therapy; still, there are practically no publications about the role of CYP3A4 polymorphisms in ALL pharmacogenomics. We genotyped eight common single-nucleotide polymorphisms (SNPs) in the CYP3A4 and CYP3A5 genes in 511 children with ALL and investigated whether they influenced the survival of the patients. We involved additional 127 SNPs in 34 candidate genes and searched for interactions with respect to the survival rates. Significant association between the survival rates and the common rs2246709 SNP in the CYP3A4 gene was observed. The gender of the patients and the rs1076991 in the MTHFD1 gene strongly influenced this effect. We calculated new risk assessments involving the gender-rs2246709 interaction and showed that they significantly outperformed the earlier risk-group assessments at every time point. If this finding is confirmed in other populations, it can have a considerable prognostic significance.
CYP3A4在急性淋巴细胞白血病(ALL)治疗中使用的许多药物的代谢过程中发挥着重要作用;然而,实际上几乎没有关于CYP3A4基因多态性在ALL药物基因组学中作用的出版物。我们对511例ALL患儿的CYP3A4和CYP3A5基因中的8个常见单核苷酸多态性(SNP)进行了基因分型,并研究它们是否影响患者的生存。我们还纳入了34个候选基因中的另外127个SNP,并搜索了与生存率相关的相互作用。观察到生存率与CYP3A4基因中常见的rs2246709 SNP之间存在显著关联。患者的性别和MTHFD1基因中的rs1076991对这种效应有强烈影响。我们计算了涉及性别-rs2246709相互作用的新风险评估,并表明它们在每个时间点都显著优于早期的风险组评估。如果这一发现能在其他人群中得到证实,它可能具有相当大的预后意义。