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Impact of YTHDF1 gene polymorphisms on Wilms tumor susceptibility: A five-center case-control study
Yanfei Liu1, Huiran Lin2, Rui-Xi Hua3
1Department of Pathology, Xi'an Children's Hospital, The Affiliated Children's Hospital of Xi'an Jiaotong University, Xi'an, China.
Insights
Genetic variants in the YTHDF1 gene were investigated for their role in childhood Wilms tumor risk. While overall risk was not associated, specific YTHDF1 polymorphisms showed age-dependent associations in Wilms tumor development.
Area of Science:
- Genetics
- Pediatric Oncology
- Molecular Biology
Background:
- Wilms tumor is the most common kidney cancer in children.
- YTHDF1 gene involvement is known in various cancers.
- The impact of YTHDF1 genetic variants on Wilms tumor risk remains unclear.
Purpose of the Study:
- To investigate the association between YTHDF1 gene single nucleotide polymorphisms (SNPs) and Wilms tumor risk.
- To analyze the influence of specific YTHDF1 SNPs (rs6011668 and rs6090311) on Wilms tumor susceptibility.
Main Methods:
- A hospital-based case-control study was conducted with 408 Wilms tumor cases and 1198 controls from China.
- Unconditional logistic regression analysis was used to assess the risk associated with YTHDF1 SNPs.
- Odds ratios (OR) and 95% confidence intervals (CI) were calculated for YTHDF1 variants rs6011668 and rs6090311.
Main Results:
- Neither rs6011668 nor rs6090311 individually showed a significant association with overall Wilms tumor risk.
- A negative association was observed for combined protective genotypes.
- Stratification analysis indicated that the rs6011668 CT/TT genotype was linked to increased risk in younger children (≤18 months) but decreased risk in older children (>18 months).
Conclusions:
- YTHDF1 gene polymorphisms may play a role in Wilms tumor risk.
- Age-specific effects of YTHDF1 variants on Wilms tumor susceptibility were identified.
Background:
Wilms tumor is the most frequent renal malignancy in children. YTHDF1 is associated with the development of several kinds of cancers, yet whether common variants of the YTHDF1 gene influence Wilms tumor risk is unknown. We present, here, a hospital-based case-control study specifically designed to investigate the role of YTHDF1 genetic variants on Wilms tumor.
Methods:
We successfully genotyped samples of 408 Wilms tumor cases and 1198 controls which were collected from five hospitals across China. The unconditional logistic regression was adopted to analyze the contributions of YTHDF1 gene single nucleotide polymorphisms (SNPs) to the risk of Wilms tumor. The odds ratio (OR) and 95% confidence interval (CI) were generated to evaluate the conferring risk of YTHDF1 gene SNPs (rs6011668 C>T, rs6090311 A>G).
Results:
Neither of the two SNPs could contribute to the risk of Wilms tumor. A negative association was also detected in the combined effects of protective genotypes on Wilms tumor risk. The stratification analysis revealed that compared with those with CC genotype, rs6011668 CT/TT genotype was associated with increased Wilms tumor risk in those ≤18 months (OR = 1.54, 95% CI = 1.02-2.30, p = 0.038), and with decreased Wilms tumor risk in those >18 months (OR = 0.70, 95% CI = 0.50-0.97, p = 0.034).
Conclusion:
Our present work sheds some light on the potential role of YTHDF1 gene polymorphisms on Wilms tumor risk.
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