Genome sequencing analysis of blood cells identifies germline haplotypes strongly associated with drug resistance in osteosarcoma patients

BMC Cancer. 2019 Apr 16;19(1):357. doi: 10.1186/s12885-019-5474-y.

Abstract

Background: Osteosarcoma is the most common malignant bone tumor in children. Survival remains poor among histologically poor responders, and there is a need to identify them at diagnosis to avoid delivering ineffective therapy. Genetic variation contributes to a wide range of response and toxicity related to chemotherapy. The aim of this study is to use sequencing of blood cells to identify germline haplotypes strongly associated with drug resistance in osteosarcoma patients.

Methods: We used sequencing data from two patient datasets, from Inova Hospital and the NCI TARGET. We explored the effect of mutation hotspots, in the form of haplotypes, associated with relapse outcome. We then mapped the single nucleotide polymorphisms (SNPs) in these haplotypes to genes and pathways. We also performed a targeted analysis of mutations in Drug Metabolizing Enzymes and Transporter (DMET) genes associated with tumor necrosis and survival.

Results: We found intronic and intergenic hotspot regions from 26 genes common to both the TARGET and INOVA datasets significantly associated with relapse outcome. Among significant results were mutations in genes belonging to AKR enzyme family, cell-cell adhesion biological process and the PI3K pathways; as well as variants in SLC22 family associated with both tumor necrosis and overall survival. The SNPs from our results were confirmed using Sanger sequencing. Our results included known as well as novel SNPs and haplotypes in genes associated with drug resistance.

Conclusion: We show that combining next generation sequencing data from multiple datasets and defined clinical data can better identify relevant pathway associations and clinically actionable variants, as well as provide insights into drug response mechanisms.

Keywords: Childhood cancers; Drug resistance; Genetics; Osteosarcoma; Pharmacogenomics; Whole genome sequencing.

MeSH terms

  • Alleles
  • Biomarkers, Tumor
  • Blood Cells / metabolism*
  • Bone Neoplasms / genetics*
  • Bone Neoplasms / mortality
  • Drug Resistance, Neoplasm / genetics*
  • Gene Frequency
  • Genomics* / methods
  • Genotype
  • Germ-Line Mutation*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Kaplan-Meier Estimate
  • Osteosarcoma / genetics*
  • Osteosarcoma / mortality
  • Polymorphism, Single Nucleotide
  • Prognosis

Substances

  • Biomarkers, Tumor