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Epithelial-mesenchymal transition in keratocystic odontogenic tumor: possible role in locally aggressive behavior.


ABSTRACT: The aim of this study is to clarify whether epithelial-mesenchymal transition (EMT) is involved in the pathogenesis and development of keratocystic odontogenic tumor (KCOT). The expression levels of EMT-related proteins and genes in normal oral mucosa (OM), radicular cyst (RC), and KCOT were determined and compared by real-time quantitative PCR and immunohistochemistry. Our data showed that the expression of epithelial markers E-cadherin and Pan-cytokeratin was significantly downregulated in KCOT with upregulation of mesenchymal markers N-cadherin compared to OM and RC. Importantly, TGF-?, a potent EMT inducer, and Slug, a master transcription factor, were also found highly expressed in KCOT. In addition, the results from Spearman rank correlation test and clustering analysis revealed the close relationship between Slug and MMP-9, which was further evidenced by double-labeling immunofluorescence that revealed a synchronous distribution for Slug with MMP-9 in KCOT samples. All the data suggested EMT might be involved in the locally aggressive behavior of KCOT.

SUBMITTER: Zhong WQ 

PROVIDER: S-EPMC4386571 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Epithelial-mesenchymal transition in keratocystic odontogenic tumor: possible role in locally aggressive behavior.

Zhong Wen-Qun WQ   Chen Gang G   Zhang Wei W   Ren Jian-Gang JG   Wu Zhong-Xing ZX   Zhao Yi Y   Liu Bing B   Zhao Yi-Fang YF  

BioMed research international 20150323


The aim of this study is to clarify whether epithelial-mesenchymal transition (EMT) is involved in the pathogenesis and development of keratocystic odontogenic tumor (KCOT). The expression levels of EMT-related proteins and genes in normal oral mucosa (OM), radicular cyst (RC), and KCOT were determined and compared by real-time quantitative PCR and immunohistochemistry. Our data showed that the expression of epithelial markers E-cadherin and Pan-cytokeratin was significantly downregulated in KCO  ...[more]

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