PDIA6 contributes to aerobic glycolysis and cancer progression in oral squamous cell carcinoma

被引:18
|
作者
Mao, Ling [1 ,2 ]
Wu, Xiaoweng [3 ]
Gong, Zhengpeng [4 ]
Yu, Ming [5 ,6 ]
Huang, Zhi [6 ,7 ]
机构
[1] Guizhou Med Univ, Hosp & Sch Stomatol, Lab Head & Neck Canc Res, Guiyang 550004, Peoples R China
[2] Liaocheng Peoples Hosp, Imaging Dept, Liaocheng, Shandong, Peoples R China
[3] Liaocheng Peoples Hosp, Dept Imaging, Guiyang 252000, Peoples R China
[4] Guizhou Med Univ, Affiliated Hosp, Dept Otorhinolaryngol, Guiyang, Peoples R China
[5] Guizhou Med Univ, Affiliated Baiyun Hosp, Laryngol & Otol, 108 Gangyu Rd, Guiyang 550005, Peoples R China
[6] Guizhou Med Univ, Affiliated Canc Hosp, Dept Intervent Radiol, Guiyang 550002, Peoples R China
[7] Guizhou Med Univ, Coll Basic Med, 1 Beijingxi Rd, Guiyang 550002, Peoples R China
关键词
PDIA6; Proliferation; Migration; Aerobic glycolysis; Tumorigenesis; PROTEIN DISULFIDE-ISOMERASE; GENE-EXPRESSION; TUMOR; PROMOTES; HEAD;
D O I
10.1186/s12957-021-02190-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/objective Accumulated evidence has demonstrated that aerobic glycolysis serves as a regulator of tumor cell growth, invasion, and angiogenesis. Herein, we explored the role of protein disulfide isomerase family 6 (PDIA6) in the aerobic glycolysis and the progression of oral squamous cell carcinoma (OSCC). Methods The expression pattern of PDIA6 in OSCC tissues was determined by qPCR and western blotting. Lentivirus and small interfering RNAs (siRNAs) were introduced into cells to upregulate and downregulate PDIA6 expression. CCK-8, flow cytometry, transwell, and xenotransplantation models were applied to detect cell proliferation, apoptosis, migration, invasion, and tumorigenesis, respectively. Results A high expression pattern of PDIA6 was observed in OSCC tissues, which was closely associated with lower overall survival and malignant clinical features in OSCC. Compared with the control group, overexpression of PDIA6 induced significant enhancements in cell growth, migration, invasiveness, and tumorigenesis and decreased cell apoptosis, while knockdown of PDIA6 caused opposite results. In addition, overexpression of PDIA6 increased glucose consumption, lactate production, and ATP level in OSCC cells. Conclusion This study demonstrated that PDIA6 expression was elevated in OSCC tissues, and overexpression of it promoted aerobic glycolysis and OSCC progression.
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页数:9
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