A Comparison of Ki67, Syndecan-1 (CD138), and Molecular RANK, RANKL, and OPG Triad Expression in Odontogenic Keratocyts, Unicystic Ameloblastoma, and Dentigerous Cysts

• Published in: Disease markers 2018-01, Vol.2018 (2018), p.1-7
• Main Authors: Sánchez-Romero, Celeste, Martinez, Guillermo, Irigoyen-Camacho, María Esther, Bologna-Molina, Ronell, Brito-Mendoza, Luisana, Mosqueda-Taylor, Adalberto
• Format: Article
• Language: English
• Subjects: Ameloblastoma; Ameloblastoma - metabolism; Archives & records; Biomarkers - metabolism; Cell cycle; Cell growth; Cloning; Comparative analysis; Cysts; Cytokines; Dentigerous Cyst - metabolism; Epithelium; Extracellular matrix; Gene Expression Regulation; Homeostasis; Humans; Immunohistochemistry; Jaw Neoplasms - metabolism; Ki-67 Antigen - metabolism; Laboratories; Lesions; Medicine; Odontogenic Cysts - metabolism; Osteoprotegerin; Osteoprotegerin - metabolism; Pathology; Population; Radiology; RANK Ligand - metabolism; Receptor Activator of Nuclear Factor-kappa B - metabolism; Stroma; Surgery; Syndecan; Syndecan-1 - metabolism; TNF inhibitors; TRANCE protein; Tumor necrosis factor-TNF; Tumors
• ISSN: 0278-0240; 1875-8630
• DOI: 10.1155/2018/7048531

Background and Objective. Reduced expression of syndecan-1 (CD138), increased proliferation index, and modifications in the expression of the molecular RANK/RANKL/OPG triad are related to an intensified potential of aggressiveness and invasion of diverse tumors and cysts. The aim was to compare the expression of Ki-67, CD138, and the molecular triad RANK, RANKL, and OPG in odontogenic keratocysts (OKC), unicystic ameloblastomas (UA), and dentigerous cysts (DC). Methods. Immunohistochemistry for Ki-67, CD138, RANK, RANKL, and OPG was performed in 58 odontogenic cystic lesions (22 OKC, 17 DC, and 19 UA). Results. A higher expression of Ki-67 was identified in OKC as compared to UA (p0.0034). RANKL was expressed higher in the epithelium (p=0.0002) and in the stroma (p=0.0004) of UA. DC had a lower expression of these markers. Conclusion. Higher RANKL expression together with the reduction on CD138 expression in UA could be linked to a greater invasive and destructive potential, while the increased proliferation rate observed in OKC could be related to its continuous intrabony growth. The expansion of DC does not seem to be related to such factors, justifying the different therapeutic approaches proposed for each of these entities.