PRDX1 is a Tumor Suppressor for Nasopharyngeal Carcinoma by Inhibiting PI3K/AKT/TRAF1 Signaling

被引:17
|
作者
Xiao, Hongmei [1 ,2 ]
Yang, Taoyu [3 ]
Yan, Lingli [4 ]
Feng, Jihong [5 ]
Huang, Boyan [6 ,7 ]
Jiang, Yu [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Med Oncol, Canc Ctr, Chengdu 610041, Peoples R China
[2] Zunyi Med Univ, Affiliated Hosp, Oncol Dept, Zunyi, Guizhou, Peoples R China
[3] Guangzhou Med Univ, Affiliated Hosp 6, Dept Invas Technol, Qingyuan 511500, Peoples R China
[4] Med Univ, Dept Immunol, Zunyi 563000, Guizhou, Peoples R China
[5] Taizhou City Peoples Hosp, Dept Oncol, Taizhou 318000, Peoples R China
[6] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, Natl Clin Res Ctr Canc, Canc Hosp, Shenzhen 518000, Peoples R China
[7] Chinese Acad Med Sci & Peking Union Med Coll, Shenzhen Hosp, Shenzhen 518000, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2020年 / 13卷
关键词
PRDX1; NPC; proliferation; migration; invasion; EMT; PI3K/AKT; TRAF1; EPITHELIAL-MESENCHYMAL TRANSITION; PEROXIREDOXIN; CONTRIBUTES; MIGRATION; CELLS;
D O I
10.2147/OTT.S252286
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Peroxiredoxin 1 (PRDX1) has been identified as a dual regulator of tumorigenesis. However, its expression, clinical significance, and biological function in nasopharyngeal carcinoma (NPC) remain unknown. This study aimed to explore the role and underlying mechanisms of PRDX1 in NPC. Materials and Methods: The expression of PRDX1 in NPC tissues was evaluated by immunohistochemistry, and the relationships between the expression of PRDX1 and clinical features and prognosis of NPC patients were analyzed. The effects of PRDX1 on NPC cell proliferation, migration, invasion, and epithelial-to-mesenchymal transition (EMT) were examined. A tumor-bearing model of nude mouse was established to verify the function of PRDX1 in vivo. Results: PRDX1 expression level was negatively associated with recurrence and metastasis of NPC. PRDX1 knockdown promoted NPC cell proliferation, migration, invasion and EMT in vitro, and enhanced tumor growth in vivo, while PRDX1 overexpression had opposite effects. Furthermore, transcriptome analysis showed that PRDX1 inhibited the activation of PI3K/AKT/TRAF1 signaling in NPC cells. Conclusion: PRDX1 inhibits NPC by inhibiting the activation of PI3K/AKT/TRAF1 signaling. PRDX1 is a tumor suppressor in human NPC and may be a prognostic biomarker for NPC patients.
引用
收藏
页码:9123 / 9133
页数:11
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