JNCI Journal of the National Cancer Institute · 2003 · 924 citations · 7 references
MedicineGeneticsOncologyCancer GeneticsMolecular OncologyNeoplasiaCancer GenomicsCancer Molecular PathologyMalignant NeoplasmsThyroid CancerBraf V600 MutationsCancer Mutation AnalysisMolecular Mechanisms Of CarcinogenesisMutationPapillary Thyroid Carcinoma PathologyThyroid Cancer GeneticsThyroid Cancer Pathology
The BRAF gene has been found to be activated by mutation in human cancers, predominantly in malignant melanoma. We tested 476 primary tumors, including 214 lung, 126 head and neck, 54 thyroid, 27 bladder, 38 cervical, and 17 prostate cancers, for the BRAF T1796A mutation by polymerase chain reaction (PCR)-restriction enzyme analysis of BRAF exon 15. In 24 (69%) of the 35 papillary thyroid carcinomas examined, we found a missense thymine (T)-->adenine (A) transversion at nucleotide 1796 in the BRAF gene (T1796A). The T1796A mutation was detected in four lung cancers and in six head and neck cancers but not in bladder, cervical, or prostate cancers. Our data suggest that activating BRAF mutations may be an important event in the development of papillary thyroid cancer.
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Mutations of the BRAF gene in human cancer
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RAF/RAS oncogenes and mismatch-repair status
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