Colorectal cancers from distinct ancestral populations show variations in BRAF mutation frequency

PLoS One. 2013 Sep 16;8(9):e74950. doi: 10.1371/journal.pone.0074950. eCollection 2013.

Abstract

It has been demonstrated for some cancers that the frequency of somatic oncogenic mutations may vary in ancestral populations. To determine whether key driver alterations might occur at different frequencies in colorectal cancer, we applied a high-throughput genotyping platform (OncoMap) to query 385 mutations across 33 known cancer genes in colorectal cancer DNA from 83 Asian, 149 Black and 195 White patients. We found that Asian patients had fewer canonical oncogenic mutations in the genes tested (60% vs Black 79% (P = 0.011) and White 77% (P = 0.015)), and that BRAF mutations occurred at a higher frequency in White patients (17% vs Asian 4% (P = 0.004) and Black 7% (P = 0.014)). These results suggest that the use of genomic approaches to elucidate the different ancestral determinants harbored by patient populations may help to more precisely and effectively treat colorectal cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Asian People
  • Black People
  • Colorectal Neoplasms / genetics*
  • Female
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Mutation Rate*
  • Proto-Oncogene Proteins B-raf / genetics*
  • White People
  • Young Adult

Substances

  • Proto-Oncogene Proteins B-raf

Grants and funding

This study was supported by the Dana-Farber Cancer Institute, the DF/HCC Pilot Program, and the Leading Foreign Research Institute Recruitment Program through the National Research Foundation of Korea (NRF) funded by the Korean Ministry of Education, Science and Technology (MEST) (2011-0030105). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.