BRAF copy number gains in thyroid tumors detected by fluorescence in situ hybridization

Endocr Pathol. 2005 Summer;16(2):99-105. doi: 10.1385/ep:16:2:099.

Abstract

Point mutation of the BRAF gene is a common genetic event in papillary thyroid carcinomas. More recently, it has been found that BRAF can also participate in chromosomal rearrangement. In this study, we explore yet another possible mechanism of BRAF alteration, which involves copy number gain. Using fluorescence in situ hybridization with BRAF specific and chromosome 7 centromeric probes, we studied 62 follicular thyroid tumors and 32 papillary carcinomas. We found that numerical changes in BRAF copy number were rare in papillary thyroid carcinomas, while they occurred in 16-45% of follicular tumors of conventional and oncocytic (Hürthle cell) types. They were due to amplification of the gene or gain of one or more copies of chromosome 7. Tetrasomy for chromosome 7 was overall the most common finding. The changes in BRAF copy number did not overlap with RAS mutations in follicular tumors. In a group of follicular carcinomas, tumors with BRAF copy number gain were significantly more often widely invasive (67%) compared to tumors with no copy number change (18%). By Western blotting, the tumors carrying four copies of the gene revealed higher expression of BRAF protein, suggesting that copy number gain may represent another mechanism of BRAF activation in thyroid tumors.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenocarcinoma, Follicular / genetics*
  • Adenocarcinoma, Follicular / pathology*
  • Biomarkers, Tumor / analysis
  • Blotting, Western
  • Carcinoma, Papillary / genetics*
  • Carcinoma, Papillary / pathology
  • Chromosomes, Human, Pair 7 / genetics
  • DNA Mutational Analysis
  • Gene Dosage*
  • Genes, ras / genetics
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Proto-Oncogene Proteins B-raf / genetics*
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / pathology

Substances

  • Biomarkers, Tumor
  • Genetic Markers
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf