Literature DB >> 19679296

Methylation frequencies of cell-cycle associated genes in epithelial odontogenic tumours.

Paula Rocha Moreira1, Mariana Moreira Guimarães, Carolina Cavaliéri Gomes, Marina Gonçalves Diniz, João Artur Ricieri Brito, Wagner Henriques de Castro, Ricardo Santiago Gomez.   

Abstract

OBJECTIVE: The benign epithelial odontogenic tumours constitute a group of lesions derived from epithelial elements of the tooth-forming apparatus. This group includes lesions of different biological behaviour, such as ameloblastoma, calcifying cystic odontogenic tumour (CCOT) and adenomatoid odontogenic tumour (AOT). The pathogenesis of these neoplasms remains uncertain and the occurrence of methylation in cell-cycle related genes may be involved in their development. The aim of this study was to investigate the methylation status of P16, P21, P27, P53 and RB1 genes in epithelial odontogenic tumours.
DESIGN: Methylation-specific polymerase chain reaction (MSP) was used to evaluate the presence of methylation in 13 samples of ameloblastoma, six samples of CCOT, three samples of AOT and 14 samples of dental follicles, included as control.
RESULTS: Our results showed a distinct methylation profile in each group. In ameloblastoma, the highest methylated genes were P16 and P21, while in CCOT the P21 and RB1 genes were the most commonly methylated genes. Only the P16 and P21 genes were methylated in the AOT samples. In the dental follicle samples, P16, P27 and RB1 genes were commonly methylated. A high percentage of the odontogenic tumours analysed showed methylation of the P21 gene, in contrast to dental follicles.
CONCLUSIONS: Epithelial odontogenic tumours show a distinct methylation profile in cell-cycle associated genes. In addition to this, the current findings show that epigenetic alterations are common events in epithelial odontogenic tumours.

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Year:  2009        PMID: 19679296     DOI: 10.1016/j.archoralbio.2009.07.006

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  8 in total

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Journal:  J Clin Exp Dent       Date:  2021-03-01

3.  A comparative immunohistochemical study of Ki-67 and Bcl-2 expression in solid ameloblastoma and adenomatoid odontogenic tumor.

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4.  Bioinformatics Analysis Reveals Genes Involved in the Pathogenesis of Ameloblastoma and Keratocystic Odontogenic Tumor.

Authors:  Eliane Macedo Sobrinho Santos; Hércules Otacílio Santos; Ivoneth Dos Santos Dias; Sérgio Henrique Santos; Alfredo Maurício Batista de Paula; John David Feltenberger; André Luiz Sena Guimarães; Lucyana Conceição Farias
Journal:  Int J Mol Cell Med       Date:  2016-12-06

5.  Multidisciplinary oral rehabilitation of an adolescent suffering from juvenile Gorlin-Goltz syndrome - a case report.

Authors:  Manfred Nilius; Jürgen Kohlhase; Johann Lorenzen; Günter Lauer; Matthias C Schulz
Journal:  Head Face Med       Date:  2019-02-08       Impact factor: 2.151

6.  Epigenetic regulation of matrix metalloproteinase expression in ameloblastoma.

Authors:  Lucyana Conceição Farias; Carolina Cavaliéri Gomes; Marcela Carolina Rodrigues; Wagner Henriques de Castro; Júlio César Tanos Lacerda; Efigênia Ferreira E Ferreira; Ricardo Santiago Gomez
Journal:  BMC Clin Pathol       Date:  2012-08-06

7.  IKKβ overexpression together with a lack of tumour suppressor genes causes ameloblastic odontomas in mice.

Authors:  Angustias Page; Ana Bravo; Cristian Suarez-Cabrera; Raquel Sanchez-Baltasar; Marta Oteo; Miguel Angel Morcillo; M Llanos Casanova; Jose C Segovia; Manuel Navarro; Angel Ramirez
Journal:  Int J Oral Sci       Date:  2020-01-02       Impact factor: 6.344

8.  Expression of DNMTs and H3K9ac in Ameloblastoma and Ameloblastic Carcinoma.

Authors:  Gleyson Kleber do Amaral-Silva; Thayná Melo de Lima Morais; Vivian Petersen Wagner; Manoela Domingues Martins; Eduardo Rodrigues Fregnani; Fernando Augusto Soares; André Caroli Rocha; Helder Rabelo Pontes; Alan Roger Santos-Silva; Pablo Agustin Vargas
Journal:  Front Oral Health       Date:  2021-10-26
  8 in total

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