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首页> 外文期刊>Leukemia and lymphoma >Investigation and analysis of single nucleotide polymorphisms in Janus kinase/signal transducer and activator of transcription genes with leukemia
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Investigation and analysis of single nucleotide polymorphisms in Janus kinase/signal transducer and activator of transcription genes with leukemia

机译:白血病Janus激酶/信号转导子和转录基因激活子中单核苷酸多态性的调查与分析

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摘要

Aberrant activation of the Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway may predispose to leukemia due to deregulation of proliferation, differentiation or apoptosis. This study was conducted to investigate whether any association exists between genetic polymorphisms in the JAK2, STAT3 and STAT5 genes and individual susceptibility to leukemia. A casecontrol study was carried out using a Chinese sample set with 344 cases of leukemia and 346 controls matched by age and ethnicity. Genomic DNA was assayed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF) on 13 single nucleotide polymorphisms (SNPs). Genotype analyses showed that two SNPs, namely rs17886724 and rs2293157 located in STAT3 and STAT5, respectively, were significantly associated with leukemia (p < 0.05 for all). Interaction analyses of SNPs (rs17886724rs2293157; rs11079041 rs2293157) showed that there were inferior associations in chronic lymphocytic leukemia (CLL) and acute myeloid leukemia (AML) compared to the control group (0.1 > p > 0.05). Linkage disequilibrium existed between rs11079041 and rs2293157 in both leukemia and control groups (r 0.7). The haplotypes displayed significant association between rs11079041 and rs2293157 in both leukemia and control groups (p < 0.05). The accuracy rate of the support vector machine (SVM) classification model in making a prediction of leukemia was 97%. The results indicated that STAT3 and STAT5 gene SNPs may be prognostic of leukemia.
机译:Janus激酶/信号转导子和转录激活子(JAK / STAT)途径的异常激活可能是由于增殖,分化或细胞凋亡的失控导致的白血病。进行该研究以调查JAK2,STAT3和STAT5基因的遗传多态性与个体对白血病的易感性之间是否存在任何关联。使用中国样本集进行了一项病例对照研究,该样本集包含344例白血病和346例年龄和种族相匹配的对照。基因组DNA通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF)对13个单核苷酸多态性(SNP)进行分析。基因型分析表明,两个SNP,分别位于STAT3和STAT5的rs17886724和rs2293157与白血病显着相关(所有p均<0.05)。 SNP(rs17886724rs2293157; rs11079041 rs2293157)的相互作用分析表明,与对照组相比,慢性淋巴细胞性白血病(CLL)和急性髓细胞性白血病(AML)的关联性较差(0.1> p> 0.05)。在白血病组和对照组中,rs11079041和rs2293157之间存在连锁不平衡(r 0.7)。在白血病组和对照组中,单倍型均显示出rs11079041和rs2293157之间的显着相关性(p <0.05)。支持向量机(SVM)分类模型在预测白血病中的准确率为97%。结果表明STAT3和STAT5基因的SNPs可能对白血病有预后。

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