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Identification of the involvement of LOXL4 in generation of keratocystic odontogenic tumors by RNA-Seq analysis
Authors:Wei-Peng Jiang  Zi-Han Sima  Hai-Cheng Wang  Jian-Yun Zhang  Li-Sha Sun  Feng Chen  Tie-Jun Li
Institution:Wei-Peng Jiang(Department of 0ral Pathology, Peking University School and Hospital of Stomatology, Beijing, China);Zi-Han Sima(Department of 0ral Pathology, Peking University School and Hospital of Stomatology, Beijing, China);Hai-Cheng Wang(Department of 0ral Pathology, Peking University School and Hospital of Stomatology, Beijing, China);Jian-Yun Zhang(Department of 0ral Pathology, Peking University School and Hospital of Stomatology, Beijing, China);Li-Sha Sun(Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, China);Feng Chen(Central Laboratory, Peking University School and Hospital of Stomatology, Beijing, China);Tie-Jun Li(Department of 0ral Pathology, Peking University School and Hospital of Stomatology, Beijing, China);
Abstract: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 (r50.882). 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.
Keywords:angiogenesis  keratocystic odontogenic tumor  lysyl oxidase-like 4  RNA-sequencing  tumor stromal fibroblast
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