Assocition between LAPTM4B gene polymorphism and the risk of childhood acute lymphoblastic leukemia

G. Bahari, M. Hashemi, M. Taheri, M. Naderi
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Abstract

Introduction : Evidence suggests that Lysosome associated protein transmembrane 4B (LAPTM4B) contributes to the risk of numerous cancers. The present study aimed to find out the impact of LAPTM4B polymorphism on the risk of childhood acute lymphoblastic leukemia (ALL) in the southeastern Iranian population. Materials and Methods : A total of 230 subjects including 110 children diagnosed with ALL and 120 healthy children enrolled in this case-control study. Genomic DNA was extracted from the whole blood by salting out method. Genotyping of LAPTM4B polymorphism was performed by polymerase chain reaction (PCR). Results: The results showed that LAPTM4B polymorphism significantly increased the risk of ALL in codominant (OR=1.91, 95% CI =1.08-3.40, p=0.025, 1/2 vs 1/1), dominant (OR=2, 95%CI=1.14-3.54, p=0.014 1/2+2/2 vs 1/1), and allele (OR = 1.74, 95% CI = 1.10–2.75, p = 0.017, 2 vs 1) genetic models Conclusion: Conclusively, our findings showed that LAPTM4B polymorphism is the risk factor of childhood ALL in our population. Further studies with larger sample sizes and different ethnicities are needed to confirm our findings.
LAPTM4B基因多态性与儿童急性淋巴细胞白血病风险的关系
有证据表明,溶酶体相关蛋白跨膜4B (LAPTM4B)与许多癌症的风险有关。本研究旨在发现LAPTM4B多态性对伊朗东南部人群儿童急性淋巴细胞白血病(ALL)风险的影响。材料与方法:本病例对照研究共纳入230例受试者,其中诊断为ALL的儿童110例,健康儿童120例。采用盐析法从全血中提取基因组DNA。采用聚合酶链反应(PCR)对LAPTM4B多态性进行基因分型。结果:结果显示,LAPTM4B多态性显著增加了共显性(OR=1.91, 95%CI= 1.08-3.40, p=0.025, 1/2 vs 1/1)、显性(OR=2, 95%CI=1.14-3.54, p=0.014 1/2+2/2 vs 1)和等位基因(OR= 1.74, 95%CI= 1.10-2.75, p= 0.017, 2 vs 1)遗传模型的ALL发病风险。结论:结论:LAPTM4B多态性是我国人群儿童ALL发病的危险因素。进一步的研究需要更大的样本量和不同的种族来证实我们的发现。
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