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Immunohistochemical expression of Rho GTPases in ameloblastomas
Author(s) -
Modolo Filipe,
Biz Michelle Tillmann,
de Sousa Suzana Machado,
Fachinelli Rodolfo de Lima,
Crema Virgínia Oliveira
Publication year - 2012
Publication title -
journal of oral pathology and medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.887
H-Index - 83
eISSN - 1600-0714
pISSN - 0904-2512
DOI - 10.1111/j.1600-0714.2011.01108.x
Subject(s) - rhoa , rhob , ameloblastoma , immunohistochemistry , gtpase , pathology , rac1 , cdc42 , biology , cancer research , tissue microarray , microbiology and biotechnology , medicine , anatomy , signal transduction , maxilla
J Oral Pathol Med (2012) 41 : 400–407 Rho GTPases are proteins that regulate cell cycle, shape, polarization, invasion, migration, and apoptosis, which are important characteristics of normal and neoplastic cells. Rho GTPases expression has been reported in normal tooth germ and several pathologies; however, it has not been evaluated in ameloblastomas. The aim of this study was to analyze the expression and distribution of RhoA, RhoB, Rac1, and Cdc42 Rho GTPases in solid and unicystic ameloblastomas. Three‐micrometer sections from paraffin‐embedded specimens were evaluated by using an avidin–biotin immunohistochemical method with antibodies against the proteins mentioned above. RhoA and RhoB staining was observed in a high number of cells ( P < 0.05) and greater intensity in non‐polarized ones. Rac1 was not observed, and Cdc42 did not show any statistical differences between the number of non‐polarized and basal positive cells ( P > 0.05). Upon comparing the studied ameloblastomas, a higher number of positive cells in the unicystic variant was observed than that in the solid one ( P < 0,05). The results obtained suggest that these GTPases could play a role in the ameloblastoma neoplastic epithelial cell phenotype determination (polarized or non‐polarized), as well as in variant (solid or unicystic) and subtype (follicular or plexiform) determination. Furthermore, they could participate in solid ameloblastoma invasion mechanisms.