Enhancing oral squamous cell carcinoma prediction: the prognostic power of the worst pattern of invasion and the limited impact of molecular resection margins
| dc.contributor.author | Hurník, Pavel | |
| dc.contributor.author | Režnarová, Jana | |
| dc.contributor.author | Chyra, Zuzana | |
| dc.contributor.author | Motyka, Oldřich | |
| dc.contributor.author | Moldovan Putnová, Barbora | |
| dc.contributor.author | Čermáková, Zuzana | |
| dc.contributor.author | Blažek, Tomáš | |
| dc.contributor.author | Fománek, Martin | |
| dc.contributor.author | Gaykalova, Daria | |
| dc.contributor.author | Buchtová, Marcela | |
| dc.contributor.author | Ševčíková, Tereza | |
| dc.contributor.author | Štembírek, Jan | |
| dc.date.accessioned | 2024-07-17T08:34:25Z | |
| dc.date.available | 2024-07-17T08:34:25Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Objective: Oral squamous cell carcinoma (OSCC) originates from the mucosal lining of the oral cavity. Almost half of newly diagnosed cases are classified as advanced stage IV disease, which makes resection difficult. In this study, we investigated the pathological features and mutation profiles of tumor margins in OSCC. Methods: We performed hierarchical clustering of principal components to identify distinct patterns of tumor growth and their association with patient prognosis. We also used next-generation sequencing to analyze somatic mutations in tumor and marginal tissue samples. Results: Our analyses uncovered that the grade of worst pattern of invasion (WPOI) is strongly associated with depth of invasion and patient survival in multivariable analysis. Mutations were primarily detected in the DNA isolated from tumors, but several mutations were also identified in marginal tissue. In total, we uncovered 29 mutated genes, mainly tumor suppressor genes involved in DNA repair including BRCA genes; however none of these mutations significantly correlated with a higher chance of relapse in our medium-size cohort. Some resection margins that appeared histologically normal harbored tumorigenic mutations in TP53 and CDKN2A genes. Conclusion: Even histologically normal margins may contain molecular alterations that are not detectable by conventional histopathological methods, but NCCN classification system still outperforms other methods in the prediction of the probability of disease relapse. | cs |
| dc.description.firstpage | art. no. 1287650 | cs |
| dc.description.source | Web of Science | cs |
| dc.description.volume | 13 | cs |
| dc.identifier.citation | Frontiers in Oncology. 2023, vol. 13, art. no. 1287650. | cs |
| dc.identifier.doi | 10.3389/fonc.2023.1287650 | |
| dc.identifier.issn | 2234-943X | |
| dc.identifier.uri | http://hdl.handle.net/10084/154848 | |
| dc.identifier.wos | 001136452500001 | |
| dc.language.iso | en | cs |
| dc.publisher | Frontiers Media S.A. | cs |
| dc.relation.ispartofseries | Frontiers in Oncology | cs |
| dc.relation.uri | https://doi.org/10.3389/fonc.2023.1287650 | cs |
| dc.rights | Copyright © 2023 Hurník, Režnarová, Chyra, Motyka, Putnová, Čermáková, Blažek, Fománek, Gaykalova, Buchtová, Ševčíková and Štembírek. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. | cs |
| dc.rights.access | openAccess | cs |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | cs |
| dc.subject | orofacial oncology | cs |
| dc.subject | squamous cell carcinoma | cs |
| dc.subject | mutation | cs |
| dc.subject | surgical margins | cs |
| dc.subject | biomarkers | cs |
| dc.title | Enhancing oral squamous cell carcinoma prediction: the prognostic power of the worst pattern of invasion and the limited impact of molecular resection margins | cs |
| dc.type | article | cs |
| dc.type.status | Peer-reviewed | cs |
| dc.type.version | publishedVersion | cs |
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