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Pre-operative evaluation of dna methylation profile in oral squamous cell carcinoma can predict tumor aggressive potential

Authors :
Sofia Asioli
Tiziana Balbi
Viscardo Paolo Fabbri
Davide B Gissi
Andrea Gabusi
Lucio Montebugnoli
Jacopo Lenzi
Luca Morandi
Sofia Melotti
Claudio Marchetti
Achille Tarsitano
Gissi D.B.
Fabbri V.P.
Gabusi A.
Lenzi J.
Morandi L.
Melotti S.
Asioli S.
Tarsitano A.
Balbi T.
Marchetti C.
Montebugnoli L.
Source :
International Journal of Molecular Sciences, Volume 21, Issue 18
Publication Year :
2020

Abstract

Background: Prognosis of oral squamous cell carcinoma (OSCC) is difficult to exactly assess on pre-operative biopsies. Since OSCC DNA methylation profile has proved to be a useful pre-operative diagnostic tool, the aim of the present study was to evaluate the prognostic impact of DNA methylation profile to discriminate OSCC with high and low aggressive potential. Methods: 36 OSCC cases underwent neoplastic cells collection by gentle brushing of the lesion, before performing a pre-operative biopsy. The CpG islands methylation status of 13 gene (ZAP70, ITGA4, KIF1A, PARP15, EPHX3, NTM, LRRTM1, FLI1, MiR193, LINC00599, MiR296, TERT, GP1BB) was studied by bisulfite Next Generation Sequencing (NGS). A Cox proportional hazards model via likelihood-based component-wise boosting was used to evaluate the prognostic power of the CpG sites. Results: The boosting estimation identified five CpGs with prognostic significance: EPHX3-24, EPHX3-26, ITGA4-3, ITGA4-4, and MiR193-3. The combination of significant CpGs provided promising results for adverse events prediction (Brier score = 0.080, C-index = 0.802 and AUC = 0.850). ITGA4 had a strong prognostic power in patients with early OSCC. Conclusions: These data confirm that the study of methylation profile provides new insights into the molecular mechanisms of OSCC and can allow a better OSCC prognostic stratification even before surgery.

Details

Language :
English
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences, Volume 21, Issue 18
Accession number :
edsair.doi.dedup.....64479d9624f256eb2746a1915743b757