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Clinical Oral Investigations

, Volume 23, Issue 2, pp 779–784 | Cite as

Immunohistochemical analysis of BRAF V600E mutation in ameloblastomas

  • Alan Motta do Canto
  • Barbara Michaela Reis da Silva Marcelino
  • Juliana Lucena Schussel
  • Bruna F. Wastner
  • Laurindo Moacir Sassi
  • Luciana Corrêa
  • Ronaldo Rodrigues de Freitas
  • Bengt Hasséus
  • Göran Kjeller
  • Celso Augusto Lemos Junior
  • Paulo Henrique Braz-SilvaEmail author
Original Article
  • 158 Downloads

Abstract

Objective

This study aimed to investigate the presence of BRAF V600E mutation in mandible ameloblastomas by correlating clinical and imaging data on the cases studied.

Methods

Eighty-four cases diagnosed as mandibular ameloblastoma were selected for analysis. The specimens were submitted to immunohistochemistry for detection of BRAF V600E mutated protein. Clinical-pathological data such as age, gender, tumour size, mandibular location, radiographic aspects, histological type and sub-type, and tumour status were collected. The clinical-pathological parameters were categorised and analysed according to BRAF V600E detection.

Results

Of the 84 patients, 78.6% (66 cases) demonstrated positivity for anti-BRAF V600E antibody, whereas 18 were negative (21.4%). The correlation between BRAF expression and variables showed statistical significances for mandibular location (P = 0.0353) and tumour size (P = 0.008), whereas no statistical significance was observed for gender, age, radiographic aspect, histological pattern, histological sub-type and tumour status. Multivariate logistic regression revealed a significant risk for BRAF positivity in tumours with posterior mandibular location (OR = 7.23, P = 0.0451) and size > 4 cm (OR = 7.29, P = 0.0150).

Conclusion

BRAF V600E mutation is common in mandibular ameloblastomas, especially in cases of tumours larger than 4 cm and in the posterior region of the mandible. In addition, this mutation can occur regardless of histological type of the tumour, age, gender, radiographic aspect and tumour status.

Clinical significance

The association between clinical-pathologic features and BRAF V600E mutation in ameloblastomas may provide directions for the treatment of this neoplasia. The use of BRAF inhibitors for targeted therapy could lead to an establishment of an alternative compared to the resective surgery.

Keywords

Ameloblastoma Odontogenic tumours Jaw Immunohistochemistry BRAFV600E mutation 

Notes

Funding

This study was supported by the Government of Brazil through the National Council for Technological Development (CNPq) according to protocol number 443004/2014-5 and São Paulo State Research Support Foundation (FAPESP) according to protocol number 2015/07727-9.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflicts of interest.

Ethical approval

All the procedures performed in our study were in accordance with the ethical standards for human research set by institutional and/or national research committees and with the 1964 Helsinki declaration, including its later amendments or comparable ethical standards. This study was approved by the Research Ethics Committee for Analysis of Research Project under protocol number (1.664.742).

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Alan Motta do Canto
    • 1
    • 2
  • Barbara Michaela Reis da Silva Marcelino
    • 1
  • Juliana Lucena Schussel
    • 3
    • 4
  • Bruna F. Wastner
    • 4
  • Laurindo Moacir Sassi
    • 4
  • Luciana Corrêa
    • 1
  • Ronaldo Rodrigues de Freitas
    • 2
  • Bengt Hasséus
    • 5
  • Göran Kjeller
    • 6
  • Celso Augusto Lemos Junior
    • 7
  • Paulo Henrique Braz-Silva
    • 1
    • 8
    Email author
  1. 1.Department of Stomatology, Division of General Pathology, School of DentistryUniversity of São PauloSão PauloBrazil
  2. 2.Unit of Oral and Maxillofacial Surgery, School of Medical SciencesIrmandade Santa Casa de São PauloSão PauloBrazil
  3. 3.Department of StomatologyFederal University of ParanáCuritibaBrazil
  4. 4.Department of Oral and Maxillofacial SurgeryErasto Gaertner HospitalCuritibaBrazil
  5. 5.Department of Oral Medicine and Pathology, Institute of Odontology, The Sahlgrenska AcademyUniversity of GothenburgGothenburgSweden
  6. 6.Department of Oral and Maxillofacial Surgery, Institute of Odontology, The Sahlgrenska AcademyUniversity of GothenburgGothenburgSweden
  7. 7.Department of Stomatology, Division of Clinical Stomatology, School of DentistryUniversity of São PauloSão PauloBrazil
  8. 8.Laboratory of Virology, Institute of Tropical Medicine of São PauloUniversity of São PauloSão PauloBrazil

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