Overexpression of ATAD2 indicates Poor Prognosis in Oral Squamous Cell Carcinoma

被引:14
|
作者
Wang, Xiao-Long [1 ,2 ,4 ]
Wang, Shuo [1 ,2 ]
Wu, Zhi-Zhong [1 ,2 ]
Yang, Qi-Chao [1 ,2 ]
Li, Hao [1 ,2 ]
Xiong, Hong-Gang [1 ,2 ]
Wan, Shu-Cheng [1 ,2 ]
Sun, Zhi-Jun [1 ,2 ,3 ]
机构
[1] Wuhan Univ, Sch & Hosp Stomatol, State Key Lab Breeding Base Basic Sci Stomatol Hu, Minist Educ, Wuhan, Peoples R China
[2] Wuhan Univ, Sch & Hosp Stomatol, Minist Educ, Key Lab Oral Biomed, Wuhan, Peoples R China
[3] Wuhan Univ, Sch & Hosp Stomatol, Dept Oral Maxillofacial Head Neck Oncol, 237 Luoyu Rd, Wuhan 430079, Peoples R China
[4] Hubei Univ Arts & Sci, Xiangyang Cent Hosp, Dept Stomatol, Affiliated Hosp, Xiangyang, Peoples R China
来源
关键词
ATAD2; oral squamous cell carcinoma; prognosis; proliferation; apoptosis; epithelial-mesenchymal transition; MESENCHYMAL TRANSITION; ATPASE-FAMILY; HEAD; CANCER; EXPRESSION; MIGRATION; INVASION; PROLIFERATION; PROGRESSION; SUPPRESSOR;
D O I
10.7150/ijms.46809
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ATPase family AAA domain-containing protein 2 (ATAD2) is highly expressed in a variety of malignancies and can promote the proliferation of tumor cells and inhibit their differentiation. However, the expression of ATAD2 and its related mechanism in oral squamous cell carcinoma (OSCC) are still unknown. Immunohistochemical staining of ATAD2, cancer stem cells (CSCs) markers and immune checkpoint molecules was conducted on human OSCC specimens to determine the expression levels of these proteins and their correlations with the clinicopathological characteristics of ATAD2 in OSCC. Moreover, the role of ATAD2 in cell proliferation, apoptosis, migration and epithelial-mesenchymal transition (EMT) were assessed by silencing ATAD2 in vitro. Immunohistochemical analysis revealed that ATAD2 expression in OSCC tissues was markedly higher than that in adjacent dysplastic tissues and normal mucosal tissues. Overexpression of ATAD2 was related to poor overall survival in OSCC patients. In addition, the protein expression of ATAD2 was notably correlated with the expression of B7-H4, PD-L1, CMTM6, Slug and ALDH1 in human OSCC. ATAD2 knockdown arrested the cell cycle, promoted the apoptosis, and inhibited the proliferation, migration, and EMT of OSCC cells. In conclusion, these findings revealed that ATAD2 is highly expressed in OSCC and can act as a poor prognostic indicator.
引用
收藏
页码:1598 / 1609
页数:12
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