Differential protein expression of osteoclastogenic factors in odontogenic cysts and tumors

• Autor(a) principal: Almeida Junior,Vildeman Rodrigues de
• Data de Publicação: 2022
• Outros Autores: Leite,Eder Gerardo Santos, Almeida,Marcus Vinicius, Castro,Jurema Freire Lisboa de, Freitas,Roseana de Almeida, Xavier,Flávia Caló Aquino, Figueiredo,Andreia Leal, Santos,Jean Nunes, Henriques,Águida Cristina Gomes
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Brazilian Oral Research
• Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242022000100263
• topic: Bone Resorption; Bone Cysts; Ameloblastoma; Biomarkers; Immunohistochemistry

Abstract: The osteolytic activity of odontogenic cysts and tumors is directly associated with their growth and aggressiveness. The influence of proteins expressed by epithelial and mesenchymal cells on this biological event differs between indolent cystic lesions, aggressive cystic lesions, and odontogenic tumors. The objective of this study was to compare the immunohistochemical expression of factors that stimulate (receptor activator of nuclear factor kappa-Β ligand – RANKL, cathepsin K – CatK and matrix metallopeptidase 8 – MMP-8) and inhibit (osteoprotegerin – OPG) osteoclastogenesis between dentigerous cyst (DC), glandular odontogenic cyst (GOC), odontogenic keratocyst (OKC), and ameloblastoma (AB). Paraffin-embedded sections of nine DCs, nine GOCs, 20 OKCs, 21 ABs, and four dental follicles (DFs) were subjected to immunohistochemistry. Immunoreactivity was analyzed semiquantitatively and quantitatively in epithelium and connective tissue, respectively. The proteins were immunoexpressed in epithelial and mesenchymal cells of all lesions studied. The expression of RANKL and CatK was higher in OKC, AB, and GOC (p<0.005). Higher expression of OPG was found in DF and DC compared to the other markers (p<0.005). MMP-8 expression was high in GOC and OKC. This study demonstrated the differential expression of factors that inhibit and stimulate bone resorption during the development of DC, GOC, OKC, and AB. Higher expression of RANKL and CatK was observed in more aggressive lesions. OPG appears to be one of the molecules responsible for the slower growth of DC.