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长链非编码 RNA 基因型对儿童白血病风险预测的新贡献

Novel Contribution of Long Non-coding RNA Genotype to Prediction of Childhood Leukemia Risk.

机构信息

Department of Pediatrics, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, Taiwan, R.O.C.

Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, R.O.C.

出版信息

Cancer Genomics Proteomics. 2022 Jan-Feb;19(1):27-34. doi: 10.21873/cgp.20301.

Abstract

BACKGROUND/AIM: Acute lymphoblastic leukemia (ALL) is frequent among children. Few studies have researched the relationship between maternally expressed gene 3 (MEG3) and cancer risk. We hypothesized long non-coding RNA MEG3 polymorphisms might influence the risk of childhood ALL.

MATERIALS AND METHODS

In a total of 266 patients with childhood ALL and 266 healthy controls, genotypes of MEG3 rs7158663, rs3087918, rs11160608 and rs4081134 single nucleotide polymorphisms were investigated for their associations with childhood ALL.

RESULTS

MEG3 rs7158663 AG and AA genotypes were significantly associated with ALL [odds ratio=1.61 (95% confidence interval=1.12-2.31) and 2.21 (1.16-4.22), respectively]. The A allele also exhibited a statistical association with higher risk of ALL (p=0.0015). There was no positive association as for rs3087918, rs11160608 or rs4081134. Interestingly, a significant interaction between MEG3 rs7158663 and age (≥3.5 years) and gender (male) was found.

CONCLUSION

MEG3 rs7158663 AG/AA genotypes were associated with higher susceptibility to childhood ALL. These novel findings should be validated in larger populations and different ethnicities.

摘要

背景/目的:急性淋巴细胞白血病(ALL)在儿童中较为常见。很少有研究探讨母源表达基因 3(MEG3)与癌症风险之间的关系。我们假设长非编码 RNA MEG3 多态性可能影响儿童 ALL 的风险。

材料和方法

在 266 例儿童 ALL 患者和 266 例健康对照者中,研究了 MEG3 rs7158663、rs3087918、rs11160608 和 rs4081134 单核苷酸多态性的基因型与儿童 ALL 之间的关系。

结果

MEG3 rs7158663 AG 和 AA 基因型与 ALL 显著相关[比值比=1.61(95%置信区间=1.12-2.31)和 2.21(1.16-4.22)]。A 等位基因也与 ALL 的发病风险呈统计学相关(p=0.0015)。rs3087918、rs11160608 或 rs4081134 与 ALL 无明显相关性。有趣的是,MEG3 rs7158663 与年龄(≥3.5 岁)和性别(男性)之间存在显著的交互作用。

结论

MEG3 rs7158663 AG/AA 基因型与儿童 ALL 的易感性增加相关。这些新发现应在更大的人群和不同的种族中进行验证。

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