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Genetic variants of AICDA/CASP14 associated with childhood brain tumor

  • S. Jeon
  • , S. Han
  • , K. Lee
  • , J. Choi
  • , S. K. Park
  • , A. K. Park
  • , H. S. Ahn
  • , H. Y. Shin
  • , H. J. Kang
  • , H. H. Koo
  • , J. J. Seo
  • , J. E. Choi
  • , H. Kim
  • , Y. Ahn
  • , D. Kang*
  • *Corresponding author for this work
  • Seoul National University
  • Korea National Open University
  • Sunchon National University
  • Sungkyunkwan University
  • University of Ulsan
  • SMG-SNU Seoul Boramae Medical Center

Research output: Contribution to journalJournal articlepeer-review

Abstract

We conducted a hospital-based case-control study in Korea to investigate whether apoptosis- and cell cycle control-related genes are associated with childhood brain tumor. Incident brain tumor cases (N = 70) and non-cancer controls (N = 140), frequency-matched by age and gender, were selected from 3 teaching hospitals in Seoul between 2003 and 2006. Tag single nucleotide polymorphisms (SNPs) (N = 297) in 30 genes related to apoptosis and cell cycle control were selected using a pairwise linkage-disequilibrium-based algorithm. Five tag SNPs in 2 genes (AICDA and CASP14) remained significant after adjusted multiple tests. The most significant association with childhood brain tumor risk was for IVS1-401G>C in the AICDA gene [odds ratio (OR) = 2.8; 95% confidence interval (95%CI) = 1.25-6.46]; the polymorphism *9276A>C of CASP14 was associated with decreased brain tumor risk (OR = 0.4; 95%CI = 0.19-0.95). We concluded that genetic polymorphisms in AICDA and CASP14 are associated with risk for brain tumor in Korean children.

Original languageEnglish
Pages (from-to)2024-2031
Number of pages8
JournalGenetics and Molecular Research
Volume12
Issue number2
DOIs
StatePublished - 2013

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Cell cycle control
  • Childhood brain tumor
  • Single nucleotide polymorphism

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