Matches in SemOpenAlex for { <https://semopenalex.org/work/W2908265365> ?p ?o ?g. }
- W2908265365 endingPage "51" @default.
- W2908265365 startingPage "43" @default.
- W2908265365 abstract "Objectives The aim of this study was to analyze and compare the immunoexpressions of Regγ, Wnt-1, and β-catenin in ameloblastomas, adenomatoid odontogenic tumors (AOTs), and odontogenic keratocysts (OKCs). Study Design Thirty solid ameloblastomas, 20 AOTs, and 30 OKCs were selected for analysis of the immunoexpression of Regγ, Wnt-1, and β-catenin. Each case was semiquantitatively evaluated in the epithelial component and in their different cellular compartments (membrane, cytoplasm, and nucleus). Results Ameloblastomas displayed higher cytoplasmic and nuclear Regγ expression compared with AOTs and OKCs, as well as higher membrane and cytoplasmic Wnt-1 expression (P < .05). β-catenin membrane expression was higher in OKCs compared with ameloblastomas and AOTs (P < .05). Nuclear β-catenin expression was higher in ameloblastomas and AOTs than in OKCs (P < .05). Cytoplasmic and nuclear Regγ expression in AOTs were positively correlated with nuclear β-catenin expression (P < .05). Conclusions The marked expressions of Regγ, Wnt-1, and β-catenin suggest the participation of these proteins in the pathogenesis of the studied lesions. The greater expressions of Regγ, Wnt-1, and nuclear β-catenin in ameloblastomas may be related to their more aggressive behavior. Pro-tumor effects of nuclear β-catenin may be counterbalanced by inhibitory pathways in AOTs, justifying their low aggressiveness. The aim of this study was to analyze and compare the immunoexpressions of Regγ, Wnt-1, and β-catenin in ameloblastomas, adenomatoid odontogenic tumors (AOTs), and odontogenic keratocysts (OKCs). Thirty solid ameloblastomas, 20 AOTs, and 30 OKCs were selected for analysis of the immunoexpression of Regγ, Wnt-1, and β-catenin. Each case was semiquantitatively evaluated in the epithelial component and in their different cellular compartments (membrane, cytoplasm, and nucleus). Ameloblastomas displayed higher cytoplasmic and nuclear Regγ expression compared with AOTs and OKCs, as well as higher membrane and cytoplasmic Wnt-1 expression (P < .05). β-catenin membrane expression was higher in OKCs compared with ameloblastomas and AOTs (P < .05). Nuclear β-catenin expression was higher in ameloblastomas and AOTs than in OKCs (P < .05). Cytoplasmic and nuclear Regγ expression in AOTs were positively correlated with nuclear β-catenin expression (P < .05). The marked expressions of Regγ, Wnt-1, and β-catenin suggest the participation of these proteins in the pathogenesis of the studied lesions. The greater expressions of Regγ, Wnt-1, and nuclear β-catenin in ameloblastomas may be related to their more aggressive behavior. Pro-tumor effects of nuclear β-catenin may be counterbalanced by inhibitory pathways in AOTs, justifying their low aggressiveness." @default.
- W2908265365 created "2019-01-11" @default.
- W2908265365 creator A5033494457 @default.
- W2908265365 creator A5037360545 @default.
- W2908265365 creator A5040570737 @default.
- W2908265365 creator A5042897430 @default.
- W2908265365 creator A5072108675 @default.
- W2908265365 creator A5079993707 @default.
- W2908265365 date "2019-07-01" @default.
- W2908265365 modified "2023-09-23" @default.
- W2908265365 title "Regulation of Wnt/β-catenin pathway may be related to Regγ in benign epithelial odontogenic lesions" @default.
- W2908265365 cites W1525435128 @default.
- W2908265365 cites W1932663550 @default.
- W2908265365 cites W1950700206 @default.
- W2908265365 cites W1980046787 @default.
- W2908265365 cites W1988021064 @default.
- W2908265365 cites W1993525179 @default.
- W2908265365 cites W1997368786 @default.
- W2908265365 cites W2002318753 @default.
- W2908265365 cites W2019231840 @default.
- W2908265365 cites W2037288942 @default.
- W2908265365 cites W2042173734 @default.
- W2908265365 cites W2042293329 @default.
- W2908265365 cites W2055011545 @default.
- W2908265365 cites W2064543034 @default.
- W2908265365 cites W2074466442 @default.
- W2908265365 cites W2117692326 @default.
- W2908265365 cites W2125793868 @default.
- W2908265365 cites W2129946268 @default.
- W2908265365 cites W2132180876 @default.
- W2908265365 cites W2134574278 @default.
- W2908265365 cites W2134878067 @default.
- W2908265365 cites W2143503616 @default.
- W2908265365 cites W2150964566 @default.
- W2908265365 cites W2161080156 @default.
- W2908265365 cites W2214552500 @default.
- W2908265365 cites W2287045820 @default.
- W2908265365 cites W2317866837 @default.
- W2908265365 cites W2465470013 @default.
- W2908265365 cites W2468227767 @default.
- W2908265365 cites W2512496368 @default.
- W2908265365 cites W2538917862 @default.
- W2908265365 cites W2546183144 @default.
- W2908265365 cites W2614891248 @default.
- W2908265365 cites W2625594949 @default.
- W2908265365 cites W2625631803 @default.
- W2908265365 cites W2734323448 @default.
- W2908265365 cites W2740063016 @default.
- W2908265365 cites W2799690174 @default.
- W2908265365 cites W2799759130 @default.
- W2908265365 cites W936568511 @default.
- W2908265365 doi "https://doi.org/10.1016/j.oooo.2018.12.019" @default.
- W2908265365 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30799234" @default.
- W2908265365 hasPublicationYear "2019" @default.
- W2908265365 type Work @default.
- W2908265365 sameAs 2908265365 @default.
- W2908265365 citedByCount "4" @default.
- W2908265365 countsByYear W29082653652021 @default.
- W2908265365 countsByYear W29082653652023 @default.
- W2908265365 crossrefType "journal-article" @default.
- W2908265365 hasAuthorship W2908265365A5033494457 @default.
- W2908265365 hasAuthorship W2908265365A5037360545 @default.
- W2908265365 hasAuthorship W2908265365A5040570737 @default.
- W2908265365 hasAuthorship W2908265365A5042897430 @default.
- W2908265365 hasAuthorship W2908265365A5072108675 @default.
- W2908265365 hasAuthorship W2908265365A5079993707 @default.
- W2908265365 hasConcept C137620995 @default.
- W2908265365 hasConcept C142724271 @default.
- W2908265365 hasConcept C190062978 @default.
- W2908265365 hasConcept C2778125672 @default.
- W2908265365 hasConcept C30145163 @default.
- W2908265365 hasConcept C502942594 @default.
- W2908265365 hasConcept C62478195 @default.
- W2908265365 hasConcept C71924100 @default.
- W2908265365 hasConcept C86803240 @default.
- W2908265365 hasConcept C95444343 @default.
- W2908265365 hasConceptScore W2908265365C137620995 @default.
- W2908265365 hasConceptScore W2908265365C142724271 @default.
- W2908265365 hasConceptScore W2908265365C190062978 @default.
- W2908265365 hasConceptScore W2908265365C2778125672 @default.
- W2908265365 hasConceptScore W2908265365C30145163 @default.
- W2908265365 hasConceptScore W2908265365C502942594 @default.
- W2908265365 hasConceptScore W2908265365C62478195 @default.
- W2908265365 hasConceptScore W2908265365C71924100 @default.
- W2908265365 hasConceptScore W2908265365C86803240 @default.
- W2908265365 hasConceptScore W2908265365C95444343 @default.
- W2908265365 hasIssue "1" @default.
- W2908265365 hasLocation W29082653651 @default.
- W2908265365 hasLocation W29082653652 @default.
- W2908265365 hasOpenAccess W2908265365 @default.
- W2908265365 hasPrimaryLocation W29082653651 @default.
- W2908265365 hasRelatedWork W1928455777 @default.
- W2908265365 hasRelatedWork W2047578621 @default.
- W2908265365 hasRelatedWork W2050712818 @default.
- W2908265365 hasRelatedWork W2320606495 @default.
- W2908265365 hasRelatedWork W2550335841 @default.
- W2908265365 hasRelatedWork W2741764772 @default.
- W2908265365 hasRelatedWork W2783287126 @default.