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Homeobox gene amplification and methylation in oral squamous cell carcinoma.
Rodrigues, Maria Fernanda Setúbal Destro; Xavier, Flávia Caló Aquino; Esteves, Carina Duarte; Nascimento, Rebeca Barros; Nobile, Juliana Stephan; Severino, Patrícia; de Cicco, Rafael; Toporcov, Tatiana Natasha; Tajara, Eloiza Helena; Nunes, Fábio Daumas.
Afiliação
  • Rodrigues MFSD; Postgraduate Program in Biophotonics Applied to Health Sciences, Nove De Julho University (UNINOVE), São Paulo, SP, Brazil.
  • Xavier FCA; Laboratory of Oral Surgical Pathology, School of Dentistry, Federal University of Bahia, Salvador, Brazil.
  • Esteves CD; Department of Oral Pathology, School of Dentistry, University of São Paulo, São Paulo, Brazil.
  • Nascimento RB; Laboratory of Oral Surgical Pathology, School of Dentistry, Federal University of Bahia, Salvador, Brazil.
  • Nobile JS; Postgraduate Program in Biophotonics Applied to Health Sciences, Nove De Julho University (UNINOVE), São Paulo, SP, Brazil.
  • Severino P; Center for Experimental Research, Albert Einstein Research and Education Institute, Hospital Israelita Albert Einstein, Sao Paulo, Brazil.
  • de Cicco R; Arnaldo Vieira de Carvalho Cancer Institute, Brazil.
  • Toporcov TN; Departament de Epidemiology, Health Public School, University of São Paulo, São Paulo, Brazil.
  • Tajara EH; Department of Molecular Biology, School of Medicine of São José do Rio Preto/FAMERP, São José do Rio Preto, SP, Brazil.
  • Nunes FD; Department of Oral Pathology, School of Dentistry, University of São Paulo, São Paulo, Brazil. Electronic address: fadnunes@usp.br.
Arch Oral Biol ; 129: 105195, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34126417
ABSTRACT

OBJECTIVES:

Investigate the DNA copy number and the methylation profile of the homeobox genes HOXA5, HOXA7, HOXA9, HOXB5, HOXB13, HOXC12, HOXC13, HOXD10, HOXD11, IRX4 and ZHX1, and correlate them with clinicopathological parameters and overall survival. MATERIAL AND

METHODS:

DNA from OSCC samples and surgical margins were submitted to DNA amplification by qPCR and to DNA methylation analysis using a DNA Methylation PCR Array System.

RESULTS:

HOXA5, HOXB5 and HOXD10 were amplified in surgical margins while HOXA9, HOXB13 and IRX4 were amplified in OSCC. HOXD10 demonstrated hypermethylation in half of the tumor while ZHX1 did not show hypermethylation. No correlation of DNA copy number or methylation with clinicopathological parameters or survival was observed.

CONCLUSION:

HOXA9, HOXB13 and IRX4 genes appears to be regulated by amplification and HOXD10 by methylation in OSCC. Further studies are needed to determine the role of these events in OSCC development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Bucais / Carcinoma de Células Escamosas / Neoplasias de Cabeça e Pescoço Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article