Expression of USP22 and the chromosomal passenger complex is an indicator of malignant progression in oral squamous cell carcinoma

被引:13
作者
Liu, Tian [1 ,2 ]
Liu, Jing [1 ,2 ]
Chen, Qiuyue [1 ]
Jin, Shengjian [1 ,2 ]
Mi, Sisi [2 ]
Shao, Wenhua [2 ]
Kudo, Yasusei [3 ]
Zeng, Sien [1 ]
Qi, Guangying [1 ,2 ]
机构
[1] Guilin Med Univ, Affiliated Hosp, Dept Pathol, 15 Lequn Rd, Guilin 541001, Guangxi, Peoples R China
[2] Guilin Med Univ, Dept Pathol & Physiopathol, 109 North 2nd Huan Cheng Rd, Guilin 541004, Guangxi, Peoples R China
[3] Tokushima Univ, Inst Biomed Sci, Dept Oral Mol Pathol, Grad Sch, Tokushima 7708504, Japan
基金
中国国家自然科学基金;
关键词
oral squamous cell carcinoma; ubiquitin-specific protease 22; survivin; aurora-B; AURORA-B; SURVIVIN EXPRESSION; POOR-PROGNOSIS; CANCER; METASTASIS; MECHANISM; BEHAVIOR; SUBUNIT; MARKER;
D O I
10.3892/ol.2018.9837
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oral cancer is a common cancer of the head and neck. Oral squamous cell carcinoma (OSCC) represents almost 90% of the total cases of head and neck cancer. Ubiquitin-specific protease 22 (USP22) is a deubiquitinating hydrolase, and it is highly expressed in various types of cancer, which also typically have a poor prognosis. Aurora-B and Survivin, which belong to the chromosomal passenger complex, are also highly expressed in a number of types of cancer. In the present study, USP22 expression and its associations with Aurora-B and Survivin, and the clinicopathological features in OSCC were explored. USP22 is highly expressed in OSCC. Overexpression of USP22 is associated with lymph node metastasis and histological grade (P<0.01). Additionally, the expression of USP22 was positively associated with Aurora-B (P<0.01), Survivin (P<0.01), and Ki-67 (P<0.01). Furthermore, USP22 small interfering RNA inhibited cell growth and reduced the expression levels of Aurora-B, Survivin and Cyclin B, together with the upregulation of cyclin-dependent kinase inhibitor 1A (p21). These data suggest that USP22, Aurora-B and Survivin promote the OSCC development and may represent novel targets for OSCC diagnosis and treatment in the future.
引用
收藏
页码:2040 / 2046
页数:7
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