Dataset Information

ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five-center case-control study.

ABSTRACT:

Background

Wilms tumor is a frequently diagnosed renal cancer among children with unclear genetic causes. N6-methyladenosine (m⁶ A) modification genes play critical roles in tumorigenesis. However, whether genetic variations of m⁶ A modification genes predispose to Wilms tumor remain unclear. ALKBH5 (AlkB homolog 5), a crucial member of m⁶ A modification genes, encodes a demethylase that functions to reverse m⁶ A RNA methylation.

Methods

Herein, we evaluated the association of single nucleotide polymorphisms (SNPs) in the m⁶ A modification gene ALKBH5 and Wilms tumor susceptibility in a large multi-center case-control study. A total of 414 Wilms tumor cases and 1199 healthy controls were genotyped for ALKBH5 rs1378602 and rs8400 polymorphisms by TaqMan.

Results

No significant association was detected between these two polymorphisms and Wilms tumor risk. Moreover, 1, 2, and 1-2 protective genotypes (rs1378602 AG/AA or rs8400 GG) did not significantly reduce Wilms tumor risk, compared with risk genotypes only. Stratification analysis revealed a significant relationship between rs1378602 AG/AA genotypes and decreased Wilms tumor risk in children in clinical stage I diseases [adjusted odds ratio (OR) = 0.56, 95% confidence interval (CI) = 0.32-0.98, P = .042]. The presence of 1-2 protective genotypes was correlated with decreased Wilms tumor risk in subgroups of age > 18 months, when compared to the absence of protective genotypes (adjusted OR = 0.74, 95% CI = 0.56-0.98, P = .035).

Conclusion

Collectively, our results demonstrate that ALKBH5 SNPs may exert a weak influence on susceptibility to Wilms tumor. This finding increases the understanding of the role of the m⁶ A gene in tumorigenesis of Wilms tumor.

SUBMITTER: Hua RX

PROVIDER: S-EPMC7307367 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Publications

ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five-center case-control study.

Hua Rui-Xi RX Liu Jiabin J Fu Wen W Zhu Jinhong J Zhang Jiao J Cheng Jiwen J Li Suhong S Zhou Haixia H Xia Huimin H He Jing J Zhuo Zhenjian Z

Journal of clinical laboratory analysis 20200224 6

<h4>Background</h4>Wilms tumor is a frequently diagnosed renal cancer among children with unclear genetic causes. N6-methyladenosine (m<sup>6</sup> A) modification genes play critical roles in tumorigenesis. However, whether genetic variations of m<sup>6</sup> A modification genes predispose to Wilms tumor remain unclear. ALKBH5 (AlkB homolog 5), a crucial member of m<sup>6</sup> A modification genes, encodes a demethylase that functions to reverse m<sup>6</sup> A RNA methylation.<h4>Methods</h4 ...[more]

PMID: 32091154

Similar Datasets

Project description:BackgroundWilms tumor is the most common pediatric renal cancer. However, genetic bases behind Wilms tumor remain largely unknown. H19 is a critical maternally imprinted gene. Previous studies indicated that single nucleotide polymorphisms (SNPs) in the H19 can modify the risk of several human malignancies. Epigenetic errors at the H19 locus lead to biallelic silencing in Wilms tumors. Genetic variations in the H19 may be related to Wilms tumor susceptibility.MethodsWe conducted a four-center study to investigate whether H19 SNP was a predisposing factor to Wilms tumor. Three polymorphisms in the H19 (rs2839698 G > A, rs3024270 C > G, rs217727 G > A) were genotyped in 355 cases and 1070 cancer-free controls, using Taqman method. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the strength of the associations.ResultsWe found that all of these three polymorphisms were significantly associated with Wilms tumor risk alterations. The rs2839698 G > A polymorphism (AG vs. GG: adjusted OR = 0.74, 95% CI = 0.57-0.96, p = 0.024; AA vs. GG: adjusted OR = 1.52, 95% CI = 1.05-2.22, p = 0.027), the rs3024270 C > G polymorphism (CG vs. CC: adjusted OR = 0.61, 95% CI = 0.46-0.81, p = 0.0007; and the rs217727 polymorphism (AG vs. GG: adjusted OR = 0.76, 95% CI = 0.58-0.99, p = 0.035). The Carriers of 1, 2, and 1-2 risk genotypes were inclined to develop Wilms tumor compared with those without risk genotype (adjusted OR = 1.36, 95% CI = 1.02-1.80, p = 0.037; adjusted OR = 1.84, 95% CI = 1.27-2.67, p = 0.001; adjusted OR = 1.50, 95% CI = 1.17-1.92, p = 0.002, respectively). The stratified analysis further revealed that rs2839698 AA, rs217727 AA, and 1-2 risk genotypes could strongly increase Wilms tumor risk among children above 18 months of age, males, and with clinical stage I+II disease.ConclusionOur findings indicate that genetic variations in the H19 may confer Wilms tumor risk.

Dataset Information

ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five-center case-control study.

Background

Methods

Results

Conclusion

Publications

ALKBH5 gene polymorphisms and Wilms tumor risk in Chinese children: A five-center case-control study.

Similar Datasets

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