Overexpression of KAI1/CD82 suppresses in vitro cell growth, migration, invasion and xenograft growth in oral cancer

被引:18
作者
Chai, Juan [1 ,2 ]
Du, Liangzhi [3 ]
Ju, Jun [2 ]
Ma, Chao [2 ]
Shen, Zhiyuan [2 ]
Yang, Xiangming [2 ]
Liang, Liang [2 ]
Ni, Qianwei [2 ]
Sun, Moyi [2 ]
机构
[1] Xian Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, 1 Xin Wang Rd, Xian 710021, Shaanxi, Peoples R China
[2] Fourth Mil Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, State Key Lab Mil Stomatol, 145 West Changle Rd, Xian 710032, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Coll Stomatol, Clin Res Ctr Shaanxi Prov Dent & Maxillofacial Di, Xian 710004, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
KAI1/CD82; oral squamous cell carcinoma; cancer; xenograft; METASTASIS SUPPRESSOR; KAI1; GENE; EXPRESSION; ASSOCIATION; ACTIVATION; MRP-1/CD9; PROTEIN; ABILITY; CD9;
D O I
10.3892/mmr.2017.6186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
KAI1/CD82 is a metastatic suppressor gene in human prostate cancer and several other types of cancer in humans. The present study aimed to examine the role of the overexpression of KAI1 in the progression of oral cancer. Human KAI1/CD82 cDNA was transfected into OSCC-15 and 293T cell lines, and its effects on OSCC-15 cell proliferation, invasion and apoptosis were assessed by performing a 3-(4, 5-dimethylthiazol-2-yl) -2, 5-diphenyltetra-zolium bromide assay, Matrigel invasion and Annexin V-FITC staining, respectively. In addition, a xenograft model was used to assess the effect of KAI1/CD82 on the in vivo growth of tumors. The overexpression of KAI1/CD82 inhibited the proliferation and invasion of OSCC-15 cells. It also enhanced the apoptotic rate of the OSCC-15 cells. Furthermore, the overexpression of KAI1/CD82 inhibited tumor growth in the xenograft model. The results demonstrated that the overexpression of KAI1/CD82 significantly inhibited the proliferation and invasion of human oral cancer cells, and inhibited tumor growth in the xenograft model. Therefore, KAI1/CD82 may be considered as a potential therapeutic target in oral cancer.
引用
收藏
页码:1527 / 1532
页数:6
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