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Leptin receptor polymorphism Gln223Arg (rs1137101) in oral squamous cell carcinoma and potentially malignant oral lesions

The purpose of this study was to assess the LEPR gene Gln223Arg polymorphism (rs1137101) in oral squamous cell carcinoma (OSCC) and in potentially malignant oral lesions (PMOL) in comparison to normal oral mucosa in a Brazilian population. Smokers (n = 89) were selected from a representative sample...

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Detalles Bibliográficos
Autores principales: Domingos, Patrícia Luciana Batista, Farias, Lucyana Conceição, Pereira, Camila Santos, das Graças Pena, Geórgia, Reis, Tatiana Carvalho, Silva, Rosângela Ramos Veloso, Fraga, Carlos Alberto de Carvalho, de Souza, Marcela Gonçalves, Soares, Mariana Batista, Jones, Kimberly Marie, Menezes, Elytania Veiga, Nobre, Sérgio Avelino Mota, Rodrigues Neto, João Felício, de Paula, Alfredo Maurício Batista, Velásquez-Meléndez, Jorge Gustavo, Sena Guimarães, André Luiz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447719/
https://www.ncbi.nlm.nih.gov/pubmed/26034683
http://dx.doi.org/10.1186/2193-1801-3-683
Descripción
Sumario:The purpose of this study was to assess the LEPR gene Gln223Arg polymorphism (rs1137101) in oral squamous cell carcinoma (OSCC) and in potentially malignant oral lesions (PMOL) in comparison to normal oral mucosa in a Brazilian population. Smokers (n = 89) were selected from a representative sample of 471 individuals from the general population of Montes Claros, Brazil. Participants were age and gender matched to patients with OSCC (n = 25) and oral epithelial dysplasia (n = 25). We investigated the LEPR Gln223Arg polymorphism (A>G; rs1137101) in these groups. Genotype variants were assessed by RFLP-PCR, using MspI (HPAII) restriction endonuclease. The institutional review board of the Universidade Estadual de Montes Claros approved the study (process number 2667/2011). Written informed consent for this study was obtained from all participants. The GG genotype (Arg223Arg) appears to be the more relevant polymorphic variant in OSCC. It occurred, approximately, twice as frequently in OSCC patients than in the general population. In contrast, the A allele in its homozygosis form (Gln223Gln) is significantly associated with the development of PMOL; 80% of the samples from the PMOL group exhibit AA genotype. Our findings suggest new insights regarding LEPR gene variations in the development of OSCC and PMOL.