Yonsei Med J.  2015 May;56(3):634-640. 10.3349/ymj.2015.56.3.634.

Detection of Plasma BRAF(V600E) Mutation Is Associated with Lung Metastasis in Papillary Thyroid Carcinomas

Affiliations
  • 1Department of Internal Medicine, School of Medicine, Pusan National University, Busan, Korea. injkim@pusan.ac.kr
  • 2Biomedical Research Institute, Busan, Korea.
  • 3Department of Otolaryngology, School of Medicine, Pusan National University, Busan, Korea.
  • 4Department of Laboratory Medicine, School of Medicine, Pusan National University, Busan, Korea.
  • 5Department of Nuclear Medicine, School of Medicine, Pusan National University, Busan, Korea.
  • 6Kim Yong Ki Internal Medicine Clinic, Busan, Korea.

Abstract

PURPOSE
The BRAF(V600E) mutation represents a novel indicator of the progression and aggressiveness of papillary thyroid carcinoma (PTC). The purpose of this study was to determine the clinical significance of free circulating mutant BRAF(V600E) in predicting the advanced disease of PTC.
MATERIALS AND METHODS
Seventy seven matched tumor and plasma samples obtained from patients with both benign and PTC were analyzed for BRAF(V600E) mutation using a peptide nucleic acid (PNA) clamp real-time polymerase chain reaction (PCR).
RESULTS
The BRAF(V600E) mutation was absent in tumor DNA samples obtained from patients with benign follicular adenomas or adenomatous goiter. In contrast, 49 of 72 (68.1%) PTC tumors were positive for the BRAF(V600E) mutation. Among them, 3 (6.1%) patients with PTC were positive for BRAF(V600E) mutation in plasma and tumor. However, all 3 patients (100%) had lateral lymph node and lung metastasis.
CONCLUSION
These findings suggest that the BRAF(V600E) mutation can be detected using a PNA clamp real-time PCR in the blood of PTC patients with lung metastasis. Future studies are warranted to determine clinical significance of serum BRAF(V600E) mutation in large prospective studies.

Keyword

BRAF; papillary thyroid carcinoma; plasma; DNA; biomarker

MeSH Terms

Adenocarcinoma, Papillary/*genetics/secondary
Adult
Aged
Carcinoma/*genetics/pathology
DNA Mutational Analysis
DNA, Neoplasm/*genetics
Female
Humans
Lung Neoplasms/*genetics
Lymph Nodes/pathology
Lymphatic Metastasis
Male
Middle Aged
Mutation
Neoplasm Invasiveness
Neoplasm Staging
*Peptide Nucleic Acids
Prospective Studies
Proto-Oncogene Proteins B-raf/*genetics
Real-Time Polymerase Chain Reaction
Thyroid Neoplasms/*genetics/pathology
DNA, Neoplasm
Peptide Nucleic Acids
Proto-Oncogene Proteins B-raf

Figure

  • Fig. 1 PNA Clamp™ standard curves in tumor DNA samples and plasma DNA sample. The detection signal was obtained by intercalation of SYBR green fluorescent dye of real-time PCR. A PNA/DNA hybrid with a single base-pair mismatch did not suppress annealing of the PCR primer (A) and amplification of mutant alleles (B). PNA, peptide nucleic acid; PCR, polemerase chain reaction; RFU, relative fluorescence units.

  • Fig. 2 Using the direct sequencing of DNA, representative sequence chromatographs from BRAF axon 15 showing wild type (A) and mutation (B) in papillary thyroid carcinomas. Arrows indicate mutations.


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