Exome sequencing reveals candidate mutations implicated in sinonasal carcinoma and malignant transformation of sinonasal inverted papilloma.
Exome sequencing
FGFR3
Genetic mutation
Head and neck cancer
Head and neck squamous cell carcinoma
Inverted papilloma
Sinonasal papilloma
Somatic variant analysis
Journal
Oral oncology
ISSN: 1879-0593
Titre abrégé: Oral Oncol
Pays: England
ID NLM: 9709118
Informations de publication
Date de publication:
01 2022
01 2022
Historique:
received:
24
06
2021
revised:
19
11
2021
accepted:
01
12
2021
pubmed:
17
12
2021
medline:
12
4
2022
entrez:
16
12
2021
Statut:
ppublish
Résumé
We explored somatic mutations in dysplastic sinonasal inverted papilloma (SNIP), SNIP with concomitant sinonasal squamous cell carcinoma (SNSCC), and SNSCC without preceding SNIP. Ten SNIP and SNSCC samples were analyzed with exome sequencing and tested for human papillomavirus. The identified mutations were compared to the most frequently mutated genes in head and neck squamous cell carcinoma (HNSCC) in the COSMIC database. Exome sequencing data were also analyzed for mutations not previously linked to SNSCC. Seven of the most commonly mutated genes in HNSCC and SNSCC in COSMIC harbored mutations in our data. In addition, we identified mutations in 23 genes that are likely to contribute to SNIP and SNSCC oncogenesis.
Identifiants
pubmed: 34915258
pii: S1368-8375(21)00770-3
doi: 10.1016/j.oraloncology.2021.105663
pii:
doi:
Types de publication
Letter
Langues
eng
Sous-ensembles de citation
IM
Pagination
105663Informations de copyright
Copyright © 2021. Published by Elsevier Ltd.