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Deep sequencing of human papillomavirus positive loco-regionally advanced oropharyngeal squamous cell carcinomas reveals novel mutational signature

Authors :
Tina Klitmøller Agander
Katalin Kiss
Estrid Høgdall
Finn Cilius Nielsen
Christian Grønhøj
David Hebbelstrup Jensen
Lena Specht
Christian von Buchwald
Frederik Otzen Bagger
Source :
BMC Cancer, Vol 18, Iss 1, Pp 1-10 (2018), Grønhøj, C, Jensen, D H, Agander, T, Kiss, K, Høgdall, E, Specht, L, Bagger, F O, Nielsen, F C & von Buchwald, C 2018, ' Deep sequencing of human papillomavirus positive loco-regionally advanced oropharyngeal squamous cell carcinomas reveals novel mutational signature ', BMC Cancer, vol. 18, no. 1, 640, pp. 1-10 . https://doi.org/10.1186/s12885-018-4567-3
Publication Year :
2017

Abstract

BACKGROUND: The genetic profile for human papilloma virus positive (HPV+) oropharyngeal squamous cell carcinomas (OPSCC) remains largely unknown. The purpose of this study was to sequence tissue material from a large cohort of locoregionally-advanced HPV+ OPSCCs.METHODS: We performed targeted deep sequencing of 395 cancer-associated genes in 114 matched tumor/normal loco-regionally advanced HPV+ OPSCCs. Mutations and copy number aberrations were determined.RESULTS: We identified a total of 3459 mutations with an average of 10 mutations per megabase and a median of 28 variants per sample. The most frequently mutated genes were KALRN (28%), SPTBN1 (32%), KMT2A (31%), ZNRF3 (9%), BNC2 (12%), NOTCH2 (25%), FGFR2 (12%), SMAD2 (6%), and AR (13%). Our findings were dominated by COSMIC signature 5 and 12, represented in other head and neck cancers and in hepatocellular carcinomas, respectively.CONCLUSIONS: We have identified multiple genetic aberrations in HPV+ OPSCCs, and the COSMIC signature 12 as most prevalent. The mutations harbour both therapeutic and prognostic potential.

Details

ISSN :
14712407
Volume :
18
Issue :
1
Database :
OpenAIRE
Journal :
BMC cancer
Accession number :
edsair.doi.dedup.....0353d6149db851bd3113af020c2d8c5f
Full Text :
https://doi.org/10.1186/s12885-018-4567-3