Journal Article

Mutational profiling can identify laryngeal dysplasia at risk of progression to invasive carcinoma

Gaafar, Ayman, Lawrie, Charles Henderson, Santaolalla, Francisco, Zabala, Aitor, López-Duque, Juan Carlos, García-Pedrero, Juana María, Manterola, Lorea, Larrea, Erika, Elorriaga, Kepa, Landa, Mikel, Larruskain, Ekhiñe, Goicoechea, Ibai, Ispizua, Ángel, Armesto, María, Rodrigo, Juan Pablo, Aguirre, Pablo, Fernández-Mercado, Marta, Municio, José Antonio, Zabalza, Ignacio, Arestín, María, Sistiaga, Jon Alexander

2018

Overview

Early diagnosis of laryngeal squamous cell carcinoma (LSCC) at the stage of dysplasia could greatly improve the outcome of affected patients. For the first time we compared the mutational landscape of non-progressing dysplasia (NPD; n = 42) with progressing dysplasia (PD; n = 24), along with patient-matched LSCC biopsies; a total of 90 samples. Using targeted next-generation sequencing identified non-synonymous mutations in six genes ( PIK3CA, FGFR3, TP53 , JAK3, MET, FBXW7 ), and mutations were validated by Sanger sequencing and/or qPCR. Analysis was extended in silico to 530 head and neck (HNSCC) cases using TCGA data. Mutations in PIK3CA and FGFR3 were detected in PD and LSCC cases, as well as other HNSCC cases, but absent in NPD cases. In contrast, mutations in JAK3 , MET and FBXW7 were found in NPD cases but not PD, LSCC or other HNSCC cases. TP53 was the most frequently mutated gene in both PD and NPD cases. With the exception of R248W, mutations were mutually exclusive. Moreover, five of seven PD mutations were located in motif H2 of p53, whereas none of the NPD mutations were. In summary, we propose that the mutational profile of laryngeal dysplasia has utility for the early detection of patients at risk of progression.

• Publisher: Nature Publishing Group UK,Nature Publishing Group
• Subject: 45/22 / 45/23 / 45/77 / 631/208/69 / 692/4028/67/69 / Cdc4 protein / Dysplasia / Fibroblast growth factor receptors / Head and neck / Humanities and Social Sciences / Invasiveness / Laryngeal cancer / multidisciplinary / Mutation / p53 Protein / Science / Science (multidisciplinary) / Squamous cell carcinoma