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Cited by 312

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

High frequency of BRAFV600E mutations in ameloblastoma

Open access
Kurppa, Kari J, Catón, Javier, Morgan, Peter R, Ristimäki, Ari, Ruhin, Blandine, Kellokoski, Jari, Elenius, Klaus, Heikinheimo, Kristiina·2014·The Journal of Pathology

Abstract

Ameloblastoma is a benign but locally infiltrative odontogenic neoplasm. Although ameloblastomas rarely metastasise, recurrences together with radical surgery often result in facial deformity and significant morbidity. Development of non‐invasive therapies has been precluded by a lack of understanding of the molecular background of ameloblastoma pathogenesis. When addressing the role of ERBB receptors as potential new targets for ameloblastoma, we discovered significant EGFR over‐expression in clinical samples using real‐time RT–PCR, but observed variable sensitivity of novel primary ameloblastoma cells to EGFR‐targeted drugs in vitro. In the quest for mutations downstream of EGFR that could explain this apparent discrepancy, Sanger sequencing revealed an oncogenic BRAF V600E mutation in the cell line resistant to EGFR inhibition. Further analysis of the clinical samples by Sanger sequencing and BRAF V600E‐specific immunohistochemistry demonstrated a high frequency of BRAF V600E mutations (15 of 24 samples, 63%). These data provide novel insight into the poorly understood molecular pathogenesis of ameloblastoma and offer a rationale to test drugs targeting EGFR or mutant BRAF as novel therapies for ameloblastoma. Published by John Wiley & Sons, Ltd. www.pathsoc.org.uk

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Metadata

Authors
Kurppa, K. J., Catón, J., Morgan, P. R., Ristimäki, A., Ruhin, B., Kellokoski, J., Elenius, K., & Heikinheimo, K.
Venue
The Journal of Pathology
Publisher
Wiley
Published
2014-01-31
Volume
232
Issue
5
Pages
492-498
ISSN
  • 0022-3417 (ISSN-L)
  • 1096-9896
OpenAlex
W1524280083
Cited by
312
References
7
FWCI
15.75
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: High frequency of BRAFV600E mutations in ameloblastoma. https://app.cochat.ai/papers/10.1002/path.4317
The paper
Kurppa, K. J., Catón, J., Morgan, P. R., Ristimäki, A., Ruhin, B., Kellokoski, J., Elenius, K., & Heikinheimo, K. (2014). High frequency of BRAFV600E mutations in ameloblastoma. The Journal of Pathology. https://doi.org/10.1002/path.4317

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.