OncoTargets and Therapy (Sep 2020)

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

  • Xiao H,
  • Yang T,
  • Yan L,
  • Feng J,
  • Huang B,
  • Jiang Y

Journal volume & issue
Vol. Volume 13
pp. 9123 – 9133

Abstract

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Hongmei Xiao,1,2 Taoyu Yang,3 Lingli Yan,4 Jihong Feng,5 Boyan Huang,6 Yu Jiang1 1Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, People’s Republic of China; 2Oncology Department, Affiliated Hospital of Zunyi Medical University, Zunyi, People’s Republic of China; 3Department of Invasive Technology, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan 511500, People’s Republic of China; 4Department of Immunology, Medical University, Zunyi 563000, Guizhou, People’s Republic of China; 5Department of Oncology, Taizhou City People’s Hospital, Taizhou 318000, People’s Republic of China; 6National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen 518000, People’s Republic of ChinaCorrespondence: Yu JiangDepartment of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, People’s Republic of ChinaEmail [email protected]: 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.Keywords: PRDX1, NPC, proliferation, migration, invasion, EMT, PI3K/AKT, TRAF1

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