Assessing pathogenic mutations in dental follicles as an attempt to identify early events in odontogenic tumours tumourigenesis

•Odontogenic tumours can originate from dental follicles.•Ameloblastomas show BRAFV600E mutatation, adenomatoid odontogenic show KRASG12R/V.•We assessed in dental follicles BRAF p.V600E and KRAS p.G12R or p.G12V.•None of the dental follicle cases tested positive for the mutations. Driver oncogenic m...

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Veröffentlicht in:Archives of oral biology 2020-05, Vol.113, p.104523-104523, Article 104523
Hauptverfasser: Coura, Bruna Pizziolo, de Resende, Taynara Asevedo Campos, de Menezes, Vinícius César Barbosa, Bernardes, Vanessa Fátima, de Sousa, Silvia Ferreira, Diniz, Marina Gonçalves, Gomez, Ricardo Santiago, Gomes, Carolina Cavalieri
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Sprache:eng
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Zusammenfassung:•Odontogenic tumours can originate from dental follicles.•Ameloblastomas show BRAFV600E mutatation, adenomatoid odontogenic show KRASG12R/V.•We assessed in dental follicles BRAF p.V600E and KRAS p.G12R or p.G12V.•None of the dental follicle cases tested positive for the mutations. Driver oncogenic mutations have been reported in several benign neoplasms. While ameloblastomas show BRAF p.V600E mutations, adenomatoid odontogenic tumours harbour either KRAS p.G12R or p.G12 V. The lack of understanding of the core molecular changes involved in tumour initiation and progression represents a critical barrier to developing new strategies for cancer detection and prevention. Considering the fact that ameloblastoma and adenomatoid odontogenic tumours can originate from dental follicles, we hypothesized that the BRAF and KRAS mutations might be early events in odontogenic tumours tumourigenesis. We aimed to assess BRAF and KRAS mutations in dental follicles associated with asymptomatic impacted teeth. Forty-eight dental follicles containing odontogenic epithelial remnants were included in the study. As ameloblastomas most often occur in the posterior mandible and adenomatoid odontogenic tumours have a predilection for the anterior jaws, we assessed by allele-specific qPCR the presence of BRAF p.V600E in 32 dental follicles associated with impacted 3rd mandibular molar teeth and KRAS p.G12 V and KRAS p.G12R mutations in 16 dental follicle specimens obtained from around impacted anterior teeth. Sanger sequencing was used as an additional method. None of the dental follicle cases tested positive for the mutations. In conclusion, we tried to detect the early genetic events associated with odontogenic tumours development in dental follicles, but we were unable to showcase that BRAF p.V600E and KRAS p.G12R or p.G12 V mutations are the early genetic events associated with odontogenic tumours development.
ISSN:0003-9969
1879-1506
DOI:10.1016/j.archoralbio.2019.104523