Functional characterization of the novel T599I-VKSRdel BRAF mutation in a follicular variant papillary thyroid carcinoma

J Clin Endocrinol Metab. 2008 Nov;93(11):4398-402. doi: 10.1210/jc.2008-0887. Epub 2008 Aug 12.

Abstract

Context: Mutations in BRAF are rare in the follicular variant of papillary thyroid carcinoma (FV-PTC).

Objective: We identified and functionally characterized a novel T599I-VKSR(600-603)del BRAF mutation in a FV-PTC patient. We analyzed in vitro the effects of this novel mutation in comparison with other thyroid cancer-associated mutations.

Design: Expression vectors for the BRAF mutants were generated and their in vitro kinase activity, signaling along the MAPK pathway, and capability of stimulating transcription from an AP1-responsive reporter evaluated.

Results: BRAF kinase and signaling were increased to a similar extent by the T599I-VKSR (600-603)del, V600E, and K601E mutations. Instead, the G474R, a mutation previously found in a FV-PTC, knocked down the BRAF kinase and its intracellular signaling. Some cancer-associated low-activity BRAF mutants stimulate the MAPK cascade via CRAF; however, the G474R protein lacked also this property.

Conclusion: The T599I-VKSR(600-603)del is a novel gain-of-function mutation that targets BRAF in FV-PTC. Moreover, G474R is the first example of a mutation knocking down enzymatic BRAF activity in a FV-PTC. These findings underscore the importance of functional studies to characterize the role of BRAF mutations associated with thyroid cancer.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Amino Acid Substitution
  • Base Sequence
  • Carcinoma, Papillary, Follicular / enzymology
  • Carcinoma, Papillary, Follicular / genetics*
  • Carcinoma, Papillary, Follicular / pathology
  • Cell Line
  • Female
  • Genes, Reporter
  • Genetic Variation*
  • Genetic Vectors
  • Humans
  • Kidney / embryology
  • Molecular Sequence Data
  • Mutation*
  • Polymorphism, Single Nucleotide*
  • Proto-Oncogene Proteins B-raf / genetics*
  • Sequence Deletion*
  • Thyroid Neoplasms / enzymology
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / pathology
  • Transfection

Substances

  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf