1. Identification of a rare 3 bp BRAF gene deletion in a thyroid nodule by mutant enrichment with 3'-modified oligonucleotides polymerase chain reaction.
- Author
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Jang MA, Lee ST, Oh YL, Kim SW, Chung JH, Ki CS, and Kim JW
- Subjects
- Alleles, Base Sequence, Carcinoma, Carcinoma, Papillary, Female, Humans, Lymphatic Metastasis, Middle Aged, Oligonucleotides genetics, Proto-Oncogene Proteins B-raf metabolism, Sequence Deletion, Thyroid Cancer, Papillary, Thyroid Neoplasms genetics, Thyroid Neoplasms pathology, Thyroid Nodule metabolism, Polymerase Chain Reaction methods, Proto-Oncogene Proteins B-raf genetics
- Abstract
Papillary thyroid carcinoma (PTC) is the most common malignant thyroid tumor, and 36-69% of PTC cases are caused by mutations in the BRAF gene. The substitution of a valine for a glutamic acid (V600E) comprises up to 95-100% of BRAF mutations; therefore, most diagnostic methods, including allele-specific PCR and real-time PCR, are designed to detect this mutation. Nevertheless, other mutations can also comprise the genetic background of PTC. Recently, a novel and sensitive technique called mutant enrichment with 3'-modified oligonucleotides (MEMO) PCR has been introduced. When we applied allelespecific PCR and MEMO-PCR for the detection of the BRAF V600E mutation, we found an unusual 3' bp deletion mutation (c.1799_1801delTGA) only when using MEMO-PCR. This deletion results in the introduction of a glutamic acid into the B-Raf activation segment (p.V600_K601delinsE), leading to an elevated basal kinase activity of BRAF. This is the first report of a rare 3 bp BRAF deletion in a PTC patient that could not be detected by allele-specific PCR.
- Published
- 2012
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