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Published on: April 1, 2019
TP53 rs1042522 C>G polymorphism and Wilms tumor susceptibility in Chinese children: a four-center case-control study
Peng Liu1, Zhenjian Zhuo2, Wenya Li3
1Department of Pediatric Intensive Care Unit, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan, China.
Insights
The TP53 rs1042522 C>G polymorphism, a variant in a tumor-suppressing gene, was investigated for its role in childhood Wilms tumor risk. This study found no significant association between this specific TP53 gene variant and Wilms tumor development in Chinese children.
Area of Science:
- Genetics
- Pediatric Oncology
- Molecular Biology
Background:
- Wilms tumor is the most frequent kidney cancer in children.
- The TP53 gene acts as a tumor suppressor by regulating cell growth.
- The TP53 rs1042522 C>G (Arg72Pro) polymorphism is studied in various cancers, but its role in Wilms tumor is unclear.
Purpose of the Study:
- To investigate the association between the TP53 rs1042522 C>G polymorphism and the risk of Wilms tumor in Chinese children.
- To determine if this specific genetic variation contributes to the development of Wilms tumor.
Main Methods:
- Genotyping of the TP53 rs1042522 C>G polymorphism in 355 Wilms tumor cases and 1070 controls from four Chinese centers.
- Analysis of the polymorphism's effect on Wilms tumor prevalence using logistic regression models.
- Stratification analysis to explore potential subgroup associations.
Main Results:
- No significant relationship was detected between the TP53 rs1042522 C>G polymorphism and the risk of Wilms tumor.
- Further stratification analyses also failed to reveal any significant associations.
- The study did not find evidence supporting the TP53 rs1042522 C>G polymorphism as a risk factor for Wilms tumor in this cohort.
Conclusions:
- The TP53 rs1042522 C>G polymorphism does not appear to significantly impact the risk of developing Wilms tumor in Chinese children.
- Larger validation studies are needed to definitively establish the role, if any, of this TP53 variant in Wilms tumor susceptibility.
- Current findings suggest this polymorphism may not be a major genetic contributor to Wilms tumor.
Abstract:
Wilms tumor is the most common renal malignancy that occurs in children. TP53 gene is considered as a tumor-suppressing gene through controlling cell growth. TP53 gene rs1042522 C>G (Arg72Pro) polymorphism is widely investigated in various types of cancers. However, it is not established if TP53 rs1042522 C>G polymorphism is a candidate variant for Wilms tumor risk. The aim of the study was to determine whether TP53 rs1042522 C>G polymorphism is responsible for the risk of Wilms tumor in Chinese children. All subjects (355 cases and 1070 controls) from four centers of China were genotyped for rs1042522 C>G polymorphism. The effect of rs1042522 C>G polymorphism on Wilms tumor prevalence was analyzed using logistic regression models. We failed to detect a significant relationship between rs1042522 C>G polymorphism and Wilms tumor risk. Further stratification analysis also could not detect a significant relationship. We conclude that TP53 rs1042522 C>G polymorphism might not have enough impact on the risk of Wilms tumor. More validation study with larger sample size will be required to better define the role of TP53 rs1042522 C>G polymorphism in Wilms tumor risk.
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