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International Journal of Oral Science ; (4): 31-38, 2014.
Article Dans Anglais | WPRIM | ID: wpr-358154

Résumé

Keratocystic odontogenic tumors (KCOT) are benign, locally aggressive intraosseous tumors of odontogenic origin. KCOT have a higher stromal microvessel density (MVD) than dentigerous cysts (DC) and normal oral mucosa. To identify genes in the stroma of KCOT involved in tumor development and progression, RNA sequencing (RNA-Seq) was performed using samples from KCOT and primary stromal fibroblasts isolated from gingival tissues. Seven candidate genes that possess a function potentially related to KCOT progression were selected and their expression levels were confirmed by quantitative PCR, immunohistochemistry and enzyme-linked immunosorbent assay. Expression of lysyl oxidase-like 4 (LOXL4), the only candidate gene that encodes a secreted protein, was enhanced at both the mRNA and protein levels in KCOT stromal tissues and primary KCOT stromal fibroblasts compared to control tissues and primary fibroblasts (P<0.05). In vitro, high expression of LOXL4 could enhance proliferation and migration of the human umbilical vein endothelial cells (HUVECs). There was a significant, positive correlation between LOXL4 protein expression and MVD in stroma of KCOT and control tissues (r=0.882). These data suggest that abnormal expression of LOXL4 of KCOT may enhance angiogenesis in KCOT, which may help to promote the locally aggressive biological behavior of KCOT.


Sujets)
Adulte , Femelle , Humains , Mâle , Jeune adulte , Amino-acid oxidoreductases , Génétique , Mouvement cellulaire , Génétique , Prolifération cellulaire , Kyste dentigère , Anatomopathologie , Évolution de la maladie , Fibroblastes , Anatomopathologie , Régulation de l'expression des gènes codant pour des enzymes , Génétique , Gencive , Anatomopathologie , Cellules endothéliales de la veine ombilicale humaine , Anatomopathologie , Microvaisseaux , Anatomopathologie , Néovascularisation pathologique , Génétique , Tumeurs odontogènes , Anatomopathologie , Analyse de séquence d'ARN , Cellules stromales , Anatomopathologie
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