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DNA 甲基转移酶 3B 基因多态性与中国汉族人群急性髓系白血病易感性的关联。

Association between DNA methyltransferases 3B gene polymorphisms and the susceptibility to acute myeloid leukemia in Chinese Han population.

机构信息

Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, China.

出版信息

PLoS One. 2013 Sep 17;8(9):e74626. doi: 10.1371/journal.pone.0074626. eCollection 2013.

Abstract

DNMT3B plays a crucial role in the generation of aberrant methylation during carcinogenesis. Polymorphisms in the DNMT3B gene may influence the DNA methylation enzymatic activity of DNMT3B, thereby modulating the susceptibility to AML. Thus, we investigated the association between SNPs in the DNMT3Bgene and their haplotypes with the risk of AML in the Chinese Han population. The DNMT3B genotype was determined by HRM in 317 de novo AML patients and 406 healthy control subjects matched for age and gender. Among the 5 SNPs investigated in this study, rs2424913 demonstrated no polymorphisms in the Chinese Han populations, rs1569686 and rs2424908 were significantly associated with AML risk. The GG genotype of rs1569686 was associated with increased AML risk (OR: 5.76; 95%CI: 2.60-12.73; P<0.01) compared with the TT genotype, and individuals with a G allele had a significantly increased risk (OR: 1.89; 95%CI: 1.41-2.52; P<0.01) for AML compared with those harboring a C allele, this polymorphism can predict the risk of AML in a minority of patients. While the CC genotype of rs2424908 appeared to reduce the AML risk (OR: 0.57; 95%CI: 0.36-0.91; P=0.01) compared with the TT genotype, individuals with a C allele were associated with a lower risk (OR: 0.79, 95%CI: 0.64-0.97, P=0.03) for developing AML compared with those harboring a T allele. The other 2 SNPs, rs6087990 and rs6119954, had no significant association with AML risk in the study population. The CGGT, CTAT, TGAT, and CGAT haplotypes of rs6087990, rs1569686, rs6119954, and rs2424908 appeared to significantly increase the AML risk, and the TTGC haplotype appeared to significantly reduce the risk. These results suggest that DNMT3B polymorphisms may contribute to the genetic susceptibility to AML; in particular, the G allele of rs1569686 serves as a risk factor for AML, whereas the C allele of rs2424908 represents a potential protective factor.

摘要

DNMT3B 在致癌过程中产生异常甲基化方面发挥着关键作用。DNMT3B 基因中的多态性可能会影响 DNMT3B 的 DNA 甲基化酶活性,从而调节 AML 的易感性。因此,我们研究了中国汉族人群中 DNMT3B 基因中的 SNPs 及其单倍型与 AML 风险之间的关联。在 317 例初诊 AML 患者和 406 例年龄和性别匹配的健康对照中,通过 HRM 确定了 DNMT3B 基因型。在本研究中研究的 5 个 SNP 中,rs2424913 在汉族人群中没有多态性,rs1569686 和 rs2424908 与 AML 风险显著相关。与 TT 基因型相比,rs1569686 的 GG 基因型与 AML 风险增加相关(OR:5.76;95%CI:2.60-12.73;P<0.01),与携带 C 等位基因的个体相比,携带 G 等位基因的个体患 AML 的风险显著增加(OR:1.89;95%CI:1.41-2.52;P<0.01),该多态性可预测少数患者的 AML 风险。与 TT 基因型相比,rs2424908 的 CC 基因型似乎降低了 AML 风险(OR:0.57;95%CI:0.36-0.91;P=0.01),与携带 C 等位基因的个体相比,携带 C 等位基因的个体患 AML 的风险较低(OR:0.79,95%CI:0.64-0.97,P=0.03)。该研究人群中,另外 2 个 SNP,rs6087990 和 rs6119954,与 AML 风险无显著关联。rs6087990、rs1569686、rs6119954 和 rs2424908 的 CGGT、CTAT、TGAT 和 CGAT 单倍型似乎显著增加 AML 风险,而 TTGC 单倍型似乎显著降低风险。这些结果表明,DNMT3B 多态性可能导致 AML 的遗传易感性;特别是 rs1569686 的 G 等位基因是 AML 的危险因素,而 rs2424908 的 C 等位基因则是潜在的保护因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc5/3775800/bdfda1030f54/pone.0074626.g001.jpg

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