The association of miR34b/c and TP53 gene polymorphisms with Wilms tumor risk in Chinese children

Author:

Wang Juxiang1,Lou Susu1,Huang Xiaokai1,Mo Yixiao1,Wang Zhen1,Zhu Jinhong2,Tian Xiaoqian1,Shi Jiandong1,Zhou Haixia1,He Jing13ORCID,Ruan Jichen1

Affiliation:

1. Department of Hematology, The Second Affiliated Hospital and Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou 325027, Zhejiang, China

2. Department of Clinical Laboratory, Biobank, Harbin Medical University Cancer Hospital, Harbin 150040, Heilongjiang, China

3. Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangdong Provincial Key Laboratory of Research in Structural Birth Defect Disease, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou 510623, Guangdong, China

Abstract

Abstract Wilms tumor is the most common pediatric malignancy in the kidney. The miR34b/c is a downstream target gene of the transcription factor p53. The important role of TP53 mutations, the methylation of miR34b/c, and the interaction between these two molecules in tumorigenesis have been well documented. Due to the biological connection between p53 and miR34b/c, in the present study, we investigated the association between polymorphisms in these two molecules and Wilms tumor susceptibility through genotyping two important functional polymorphisms (miR34b/c rs4938723 T>C and TP53 rs1042522 C>G) in 183 cases and 603 controls. Adjusted odds ratios (ORs) and 95% confidence intervals (CIs) derived from the logistic regression analysis were used to assess the correlation of miR34b/c rs4938723 and TP53 rs1042522 polymorphisms with Wilms tumor risk. Our results indicated that the association of miR34b/c rs4938723 and TP53 rs1042522 polymorphisms with Wilms tumor susceptibility was not statistically significant. Stratified analysis by age, gender, and clinical stage, as well as combined effect analysis were also performed, yet, no significant association was found. In conclusion, our study indicated a lack of association between the two selected polymorphisms and Wilms tumor susceptibility. Our findings need to be verified in studies with larger sample size in the future.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference43 articles.

1. Association of chromosome 1q gain with inferior survival in favorable-histology Wilms tumor: a report from the Children’s Oncology Group;Gratias;J. Clin. Oncol.,2016

2. Re: Risk of adverse health and social outcomes up to 50 years after Wilms tumor: The British Childhood Cancer Survivor Study;Canning;J. Urol.,2018

3. Mutations in the transcriptional repressor REST predispose to Wilms tumor;Mahamdallie;Nat. Genet.,2015

4. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour;Hanks;Nat. Commun.,2014

5. Fine structure analysis of the WT1 gene in sporadic Wilms tumors;Varanasi;Proc. Natl. Acad. Sci. U.S.A.,1994

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