Association of three polymorphisms in ARID5B, IKZF1and CEBPE with the risk of childhood acute lymphoblastic leukemia in a Chinese population

IF 2.6 3区 生物学 Q2 GENETICS & HEREDITY Gene Pub Date : 2013-07-25 DOI:10.1016/j.gene.2013.04.028
Yaping Wang , Jing Chen , Jie Li , Jianping Deng , Yaoyao Rui , Qin Lu , Meilin Wang , Na Tong , Zhengdong Zhang , Yongjun Fang
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引用次数: 54

Abstract

Recent genome-wide association studies (GWAS) that focus on childhood acute lymphoblastic leukemia (ALL), the most common malignancy in children younger than 15 years old, have found evidence that single nucleotide polymorphisms (SNPs) in IKZF1 (7p12.2), ARID5B (10q21.2) and CEBPE (14q11.2) are strongly related to the risk of childhood ALL. These polymorphisms may lead to abnormal expression and dysfunction of the corresponding transcription factors and are likely to increase the risk of ALL. To validate the relationship between these SNPs and the risk of childhood ALL in Chinese population, we conducted a case–control study of 570 ALL cases and 673 controls. We determined that the SNP rs10821936 in ARID5B was statistically significantly associated with the risk of childhood ALL (P < 0.0001). The results were also significant for the subgroup analysis of high-risk, medium-risk and low-risk ALL as well as B-lineage ALL. Statistically significant differences were not found in the SNPs for IKZF1 and CEBPE. In conclusion, ARID5B rs10821936 could serve as a potential biomarker for assessing the risk of childhood ALL in Chinese children.

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中国人群中ARID5B、ikzf1和CEBPE三种多态性与儿童急性淋巴细胞白血病风险的关联
最近的全基因组关联研究(GWAS)关注儿童急性淋巴细胞白血病(ALL),这是15岁以下儿童中最常见的恶性肿瘤,已经发现IKZF1 (7p12.2), ARID5B (10q21.2)和CEBPE (14q11.2)的单核苷酸多态性(snp)与儿童ALL的风险密切相关。这些多态性可能导致相应转录因子的异常表达和功能障碍,并可能增加ALL的风险。为了验证这些snp与中国人群儿童期ALL风险之间的关系,我们对570例ALL病例和673例对照进行了病例对照研究。我们确定ARID5B中的SNP rs10821936与儿童ALL的风险有统计学意义(P <0.0001)。该结果对于高危、中危、低危ALL以及b系ALL的亚组分析也具有重要意义。IKZF1和CEBPE的snp差异无统计学意义。综上所述,ARID5B rs10821936可作为评估中国儿童ALL风险的潜在生物标志物。
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来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
期刊最新文献
Population genetic structure of the fibrinogen-related protein 1 (FREP1) in Iranian isolates of Anopheles stephensi as a promising mosquito-based malaria vaccine candidate. Prognostic gene expression profile of colorectal cancer. Editorial Board Human-genetic variants associated with susceptibility to SARS-CoV-2 infection. miR-660: A novel regulator in human cancer pathogenesis and therapeutic implications.
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