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

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http://hdl.handle.net/10138/312881

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Kelppe , J , Thoren , H , Ristimäki , A , Haglund , C , Sorsa , T & Hagström , J 2019 , ' BRAF V600E expression in ameloblastomas-A 36-patient cohort from Helsinki University Hospital ' , Oral Diseases , vol. 25 , no. 4 , pp. 1169-1174 . https://doi.org/10.1111/odi.13072

Title: BRAF V600E expression in ameloblastomas-A 36-patient cohort from Helsinki University Hospital
Author: Kelppe, Jetta; Thoren, Hanna; Ristimäki, Ari; Haglund, Caj; Sorsa, Timo; Hagström, Jaana
Contributor organization: Department of Pathology
University of Helsinki
Medicum
Clinicum
HUSLAB
Gastrointestinal tumorigenesis
Genome-Scale Biology (GSB) Research Program
Research Programs Unit
Department of Surgery
II kirurgian klinikka
Department of Oral and Maxillofacial Diseases
Timo Sorsa / Principal Investigator
Suu- ja leukakirurgian yksikkö
HUS Head and Neck Center
HUS Abdominal Center
Date: 2019-05
Language: eng
Number of pages: 6
Belongs to series: Oral Diseases
ISSN: 1354-523X
DOI: https://doi.org/10.1111/odi.13072
URI: http://hdl.handle.net/10138/312881
Abstract: 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. 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. 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. Conclusions An immunohistochemical BRAF marker could be a beneficial tool to predict the outcome of patients with this aggressive, easily recurring tumor.
Subject: ameloblastoma
BRAF
immunohistochemistry
MUTATIONS
313 Dentistry
3126 Surgery, anesthesiology, intensive care, radiology
Peer reviewed: Yes
Usage restriction: openAccess
Self-archived version: acceptedVersion


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