TY - JOUR T1 - A Sensitive Peptide Nucleic Acid Probe Assay for Detection of <em>BRAF</em> V600 Mutations in Melanoma JF - Cancer Genomics - Proteomics JO - Cancer Genomics Proteomics SP - 381 LP - 386 VL - 13 IS - 5 AU - TAI-LONG CHEN AU - JOHN WEN-CHENG CHANG AU - JIA-JUAN HSIEH AU - HSIN-YI CHENG AU - CHIUAN-CHIAN CHIOU Y1 - 2016/09/01 UR - http://cgp.iiarjournals.org/content/13/5/381.abstract N2 - Mutated v-Raf murine sarcoma viral oncogene homolog B (BRAF) is an important biomarker for the prediction of therapeutic efficacy of several anticancer drugs. The detection of BRAF mutation faces two challenges: Firstly, there are multiple types of mutations, and secondly, tumor samples usually contain various amounts of wild-type, normal tissues. Here, we describe a newly established method for sensitive detection of multiple types of BRAF V600 mutations in excess wild-type background. The method introduced a fluorophore-tagged peptide nucleic acid (PNA) to serve as both polymerase chain reaction (PCR) clamp and sensor probe, which inhibited the amplification of wild-type templates during PCR and revealed multiple types of mutant signals during melting analysis. We demonstrated the design and optimization process of the method, and applied it in the detection of BRAF mutations in 49 melanoma samples. This PNA probe assay method detected three types of mutations in 17 samples, and was much more sensitive than conventional PCR plus Sanger sequencing. ER -