An immunohistochemical and genetic study of BRAFV600E mutation in Japanese patients with ameloblastoma.

Abstract:

:Ameloblastoma is an odontogenic tumor of the jaw. It most frequently occurs in the mandible, and less often in the maxilla. Mandibular ameloblastoma harbors a BRAF mutation that causes a valine (V) to glutamic acid (E) substitution at codon 600 (BRAFV600E ). We examined specimens from 32 Japanese patients to detect the prevalence of the BRAFV600E mutation, and to evaluate the relationship between immunohistochemical (IHC) expression and genetic results, of BRAFV600E+ ameloblastoma. Among the 32 cases, 22 (69%) were IHC positive for BRAFV600E protein, and 10 (31%) were IHC negative; and polymerase chain reaction showed 16 of 21 tested cases (76%) carried the BRAFV600E mutation. Our findings indicate that that samples that stain IHC positive for BRAFV600E protein are more likely to carry the BRAFV600E mutation. These results support assessments for BRAF mutations, and the use of BRAF inhibitors as targeted therapy for ameloblastoma in Japanese patients.

journal_name

Pathol Int

journal_title

Pathology international

authors

Seki-Soda M,Sano T,Ito K,Yokoo S,Oyama T

doi

10.1111/pin.12899

subject

Has Abstract

pub_date

2020-04-01 00:00:00

pages

224-230

issue

4

eissn

1320-5463

issn

1440-1827

journal_volume

70

pub_type

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