| Literature DB >> 28552549 |
Maria Currás-Freixes1, Elena Piñeiro-Yañez2, Cristina Montero-Conde1, María Apellániz-Ruiz1, Bruna Calsina1, Veronika Mancikova1, Laura Remacha1, Susan Richter3, Tonino Ercolino4, Natalie Rogowski-Lehmann5, Timo Deutschbein6, María Calatayud7, Sonsoles Guadalix7, Cristina Álvarez-Escolá8, Cristina Lamas9, Javier Aller10, Julia Sastre-Marcos11, Conxi Lázaro12, Juan C Galofré13, Ana Patiño-García14, Amparo Meoro-Avilés15, Judith Balmaña-Gelpi16, Paz De Miguel-Novoa17, Milagros Balbín18, Xavier Matías-Guiu19, Rocío Letón1, Lucía Inglada-Pérez20, Rafael Torres-Pérez1, Juan M Roldán-Romero1, Cristina Rodríguez-Antona20, Stephanie M J Fliedner21, Giuseppe Opocher22, Karel Pacak23, Esther Korpershoek24, Ronald R de Krijger25, Laurent Vroonen26, Massimo Mannelli4, Martin Fassnacht6, Felix Beuschlein5, Graeme Eisenhofer27, Alberto Cascón20, Fátima Al-Shahrour2, Mercedes Robledo28.
Abstract
Genetic diagnosis is recommended for all pheochromocytoma and paraganglioma (PPGL) cases, as driver mutations are identified in approximately 80% of the cases. As the list of related genes expands, genetic diagnosis becomes more time-consuming, and targeted next-generation sequencing (NGS) has emerged as a cost-effective tool. This study aimed to optimize targeted NGS in PPGL genetic diagnostics. A workflow based on two customized targeted NGS assays was validated to study the 18 main PPGL genes in germline and frozen tumor DNA, with one of them specifically directed toward formalin-fixed paraffin-embedded tissue. The series involved 453 unrelated PPGL patients, of whom 30 had known mutations and were used as controls. Partial screening using Sanger had been performed in 275 patients. NGS results were complemented with the study of gross deletions. NGS assay showed a sensitivity ≥99.4%, regardless of DNA source. We identified 45 variants of unknown significance and 89 pathogenic mutations, the latter being germline in 29 (7.2%) and somatic in 58 (31.7%) of the 183 tumors studied. In 37 patients previously studied by Sanger sequencing, the causal mutation could be identified. We demonstrated that both assays are an efficient and accurate alternative to conventional sequencing. Their application facilitates the study of minor PPGL genes, and enables genetic diagnoses in patients with incongruent or missing clinical data, who would otherwise be missed.Entities:
Mesh:
Year: 2017 PMID: 28552549 PMCID: PMC5500830 DOI: 10.1016/j.jmoldx.2017.04.009
Source DB: PubMed Journal: J Mol Diagn ISSN: 1525-1578 Impact factor: 5.568