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Identification of Novel SNPs in Glioblastoma Using Targeted Resequencing

Public Library of Science
Publication Date
DOI: 10.1371/journal.pone.0018158
  • Research Article
  • Biology
  • Computational Biology
  • Genomics
  • Genome Analysis Tools
  • Genome-Wide Association Studies
  • Microarrays
  • Genetics
  • Human Genetics
  • Population Genetics
  • Genetic Polymorphism
  • Cancer Genetics
  • Genomic Medicine
  • Medicine
  • Oncology
  • Cancers And Neoplasms
  • Neurological Tumors
  • Glioblastoma Multiforme
  • Biology
  • Medicine


High-throughput sequencing opens avenues to find genetic variations that may be indicative of an increased risk for certain diseases. Linking these genomic data to other “omics” approaches bears the potential to deepen our understanding of pathogenic processes at the molecular level. To detect novel single nucleotide polymorphisms (SNPs) for glioblastoma multiforme (GBM), we used a combination of specific target selection and next generation sequencing (NGS). We generated a microarray covering the exonic regions of 132 GBM associated genes to enrich target sequences in two GBM tissues and corresponding leukocytes of the patients. Enriched target genes were sequenced with Illumina and the resulting reads were mapped to the human genome. With this approach we identified over 6000 SNPs, including over 1300 SNPs located in the targeted genes. Integrating the genome-wide association study (GWAS) catalog and known disease associated SNPs, we found that several of the detected SNPs were previously associated with smoking behavior, body mass index, breast cancer and high-grade glioma. Particularly, the breast cancer associated allele of rs660118 SNP in the gene SART1 showed a near doubled frequency in glioblastoma patients, as verified in an independent control cohort by Sanger sequencing. In addition, we identified SNPs in 20 of 21 GBM associated antigens providing further evidence that genetic variations are significantly associated with the immunogenicity of antigens.

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