A study on the inhibition of VEGF expression in salivary gland adenoid cystic carcinoma cells via iNOS gene RNAi in vitro

被引:8
作者
Yang, Ke-Xiong Ou [1 ,2 ]
Liang, Jun [3 ]
Yang, Zi-Nan [2 ]
Zhao, Jian-Jiang [1 ]
机构
[1] Southern Med Univ, Guangdong Prov Stomatol Hosp, Dept Oral & Maxillofacial Surg, Guangzhou 510280, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Dept Oral & Maxillofacial Surg, Stomatol Hosp, Guangzhou, Guangdong, Peoples R China
[3] Sun Yet Sen Univ, Affiliated Hosp 5, Dept Oral & Maxillofacial Surg, Zhuhai, Peoples R China
关键词
inducible nitric oxide synthase; RNA interference; salivary gland adenoid cystic carcinoma; vascular endothelial growth factor; ENDOTHELIAL-GROWTH-FACTOR; NITRIC-OXIDE-SYNTHASE; KAPPA-B; APOPTOSIS; ANGIOGENESIS; PROGNOSIS; CANCER;
D O I
10.1111/jop.12217
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
In this study, we aimed to explore the effect of inducible nitric oxide synthase (iNOS) on vascular endothelial growth factor (VEGF) expression in salivary gland adenoid cystic carcinoma (SACC). Using RNAi, we transfected chemically synthesised iNOS siRNA into ACC-M cells (a highly metastatic adenoid cystic carcinoma cell line) and detected the change in the gene and protein expression levels of iNOS and VEGF by qRT-PCR and Western blotting. A transwell invasiveness assay was used to examine the changes in invasive ability of ACC-M cells. Cell growth was determined using a CCK-8 assay. Apoptosis and cell-cycle phases were detected by flow cytometry. We found that silencing iNOS down-regulated the expression of VEGF and then inhibited cell growth and invasiveness of SACC cells, while it increased apoptosis. Therefore, we concluded that iNOS can regulate VEGF expression and iNOS may be a therapeutic target.
引用
收藏
页码:153 / 158
页数:6
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