Identification of novel genes by whole-exome sequencing can improve gastric cancer precision oncology

Future Oncol. 2017 Apr;13(10):883-892. doi: 10.2217/fon-2016-0430. Epub 2016 Nov 29.

Abstract

Aim: By identifying cancer driver genes involved in tumorigenesis, whole-exome sequencing (WES) analyses enable the development of robust biomarkers and novel therapeutic targets to reach precision oncology.

Patients & methods: WES analyses were performed in matched gastric cancer-normal gastric tissues from two patients. We compared genes highlighted with those of a database and recent WES/whole-genome sequencing studies.

Results: We identified 32 highlighted gastric cancer genes, two of these (DEFB118 and RNF43) may provide future potential clinical implications.

Conclusion: Definitive evidence on extensive genetic heterogeneity suggests the need for large-scale next-generation sequencing studies to validate gastric cancer driver genes catalog. This list represents the foundation for developing genome-based biomarkers to guide precision gastric cancer treatment.

Keywords: biomarkers; next-generation sequencing analyses; personalized cancer medicine; therapeutic targets; whole-exome sequencing; whole-genome sequencing.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers
  • Computational Biology / methods
  • DNA Copy Number Variations
  • Exome*
  • Female
  • Genetic Association Studies*
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • INDEL Mutation
  • Male
  • Middle Aged
  • Mutation
  • Neoplasm Grading
  • Neoplasm Staging
  • Polymorphism, Single Nucleotide
  • Precision Medicine
  • Prognosis
  • Stomach Neoplasms / diagnosis*
  • Stomach Neoplasms / genetics*

Substances

  • Biomarkers