BRAF V600E expression in ameloblastomas-A 36-patient cohort from Helsinki University Hospital

dc.contributor.authorJetta Kelppe
dc.contributor.authorHanna Thorén
dc.contributor.authorAri Ristimäki
dc.contributor.authorCaj Haglund
dc.contributor.authorTimo Sorsa
dc.contributor.authorJaana Hagström
dc.contributor.organizationfi=hammaslääketieteen laitos|en=Institute of Dentistry|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.64787032594
dc.converis.publication-id40203941
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/40203941
dc.date.accessioned2025-08-28T03:21:27Z
dc.date.available2025-08-28T03:21:27Z
dc.description.abstract<div>Objectives: We aimed to investigate BRAF V600E percentage immunohistochemically in ameloblastomas of a single institute cohort. We were interested if age, location, histological properties, or tumor recurrence depend on the BRAF status.</div><div><br /></div><div> Subjects, materials and methods: We had 36 formalin-fixed, paraffin-embedded ameloblastoma tissue samples of patients treated at the Helsinki University Hospital between the years 1983-2016. Tissue sections underwent immunohistochemistry by Ventana BenchMark XT immunostainer using Ms Anti-Braf V600E (VE1) MAB. We used R 3.4.2 and RStudio 1.1.383 to conduct statistical analysis for BRAF positivity and earlier onset as well as tumor location. We used chi-squared tests and 2-by-2 table functions to determine connections between BRAF positivity and recurrence, growth pattern, and type. <br /></div><div><br /></div><div>Results: BRAF-positive tumors occurred in younger patients compared to BRAF-negative tumors (p = 0.015) and they located mostly to the mandible (p < 0.001). Growth patterns were limited to two in BRAF-negative tumors when BRAF-positive tumors presented with one to four growth patterns (p = 0.02). None of the maxillary tumors showed BRAF positivity and of these, 72.2% recurred.</div><div><br /></div><div> Conclusions: An immunohistochemical BRAF marker could be a beneficial tool to predict the outcome of patients with this aggressive, easily recurring tumor.</div>
dc.format.pagerange1169
dc.format.pagerange1174
dc.identifier.eissn1601-0825
dc.identifier.jour-issn1354-523X
dc.identifier.olddbid210568
dc.identifier.oldhandle10024/193595
dc.identifier.urihttps://www.utupub.fi/handle/11111/52160
dc.identifier.urnURN:NBN:fi-fe2021042826728
dc.language.isoen
dc.okm.affiliatedauthorThoren, Hanna
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline313 Dentistryen_GB
dc.okm.discipline313 Hammaslääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1111/odi.13072
dc.relation.ispartofjournalOral Diseases
dc.relation.issue4
dc.relation.volume25
dc.source.identifierhttps://www.utupub.fi/handle/10024/193595
dc.titleBRAF V600E expression in ameloblastomas-A 36-patient cohort from Helsinki University Hospital
dc.year.issued2019

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