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Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma

  • Authors:
    • Min Xue
    • Weimin Tao
  • View Affiliations / Copyright

    Affiliations: Department of Respiratory Medicine, Shanghai Minhang Hospital, Fudan University, Shanghai 201199, P.R. China, SICU, Tongren Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200336, P.R. China
    Copyright: © Xue et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 2637-2646
    |
    Published online on: September 7, 2017
       https://doi.org/10.3892/or.2017.5948
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Abstract

Lung adenocarcinoma (LAC) is currently the predominant histological subtype of lung cancer. Despite recent advancement in targeted therapies, the average 5-year survival rate is only 15%, highlighting the need to identify previously unrecognized molecular events that propel cancer development. Herein, we showed knockdown of 14-3-3ζ suppresses cell proliferation, migration and invasion capability of A549 and H1299 cells. MUC1 was then identified as a novel target of 14-3-3ζ protein. Overexpression of MUC1 is found to induce epithelial-mesenchymal transition and promote metastasis of lung cancer cells, while knockdown of 14-3-3ζ can completely abolish the oncogenic function of MUC1.Furthermore, we unraveled a novel mechanism that 14-3-3ζ activates NF-κB signaling pathway, and therefore enhanced MUC1/NF-κB feedback loop to upregulate MUC1 expression. From a clinical point of view, we evaluated the expression of14-3-3ζ and MUC1 in GSE68465 datasets, in which high expression of14-3-3ζ and MUC1 emerged as poor prognostic factors in LAC patients. In conclusion, we provide novel evidence that 14-3-3ζ regulates MUC1 through MUC1/NF-κB feedback loop. 14-3-3ζ and MUC1 is a promising prognostic biomarker for lung cancer patients and therapeutic targeting of 14-3-3ζ and MUC1 may be a potential treatment option for patients with LAC.
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Copy and paste a formatted citation
Spandidos Publications style
Xue M and Tao W: Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma. Oncol Rep 38: 2637-2646, 2017.
APA
Xue, M., & Tao, W. (2017). Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma. Oncology Reports, 38, 2637-2646. https://doi.org/10.3892/or.2017.5948
MLA
Xue, M., Tao, W."Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma". Oncology Reports 38.5 (2017): 2637-2646.
Chicago
Xue, M., Tao, W."Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma". Oncology Reports 38, no. 5 (2017): 2637-2646. https://doi.org/10.3892/or.2017.5948
Copy and paste a formatted citation
x
Spandidos Publications style
Xue M and Tao W: Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma. Oncol Rep 38: 2637-2646, 2017.
APA
Xue, M., & Tao, W. (2017). Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma. Oncology Reports, 38, 2637-2646. https://doi.org/10.3892/or.2017.5948
MLA
Xue, M., Tao, W."Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma". Oncology Reports 38.5 (2017): 2637-2646.
Chicago
Xue, M., Tao, W."Upregulation of MUC1 by its novel activator 14-3-3ζ promotes tumor invasion and indicates poor prognosis in lung adenocarcinoma". Oncology Reports 38, no. 5 (2017): 2637-2646. https://doi.org/10.3892/or.2017.5948
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