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Article

MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis

  • Authors:
    • Cui-Ping Wang
    • Yong-Zheng Yu
    • Hui Zhao
    • Li-Juan Xie
    • Qi-Tang Wang
    • Ye Wang
    • Qiang Mu
  • View Affiliations / Copyright

    Affiliations: The First Department of Breast Surgery, Qingdao Central Hospital, The Second Affiliated Hospital of Medical College of Qingdao University, Qingdao, Shandong 266042, P.R. China, Department of Ophthalmology, Qingdao Women and Children's Hospital, Qingdao University, Qingdao, Shandong 266034, P.R. China, Clinical Laboratory, Qingdao Central Hospital, The Second Affiliated Hospital of Medical College of Qingdao University, Qingdao, Shandong 266042, P.R. China
  • Article Number: 127
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    Published online on: May 11, 2021
       https://doi.org/10.3892/or.2021.8078
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Abstract

MicroRNAs are important for the regulation of multiple cellular functions and are involved in the initiation and progression of various types of cancer, including breast cancer. Although microRNA (miR)‑454‑3p is reported to function as an oncogene in several types of human cancer, the role of miR‑454‑5p in breast cancer remains unknown. The present study demonstrated that miR‑454‑5p was upregulated in breast cancer and was associated with a poor prognosis in patients with breast cancer. Overexpression of miR‑454‑5p promoted breast cancer cell viability, migration and invasion in vitro, whereas silencing of miR‑454‑5p inhibited breast cancer proliferation, migration and invasion in vitro and suppressed tumor growth in vivo. Mechanistically, forkhead box J2 (FoxJ2) was shown to be a target of miR‑454‑5p and transactivated E‑cadherin expression. Moreover, silencing of miR‑454‑5p reversed the epithelial‑mesenchymal transition phenotype through upregulation of the FoxJ2/E‑cadherin axis. Collectively, the present findings suggested that miR‑454‑5p may serve as a novel therapeutic target and prognostic predictor for patients with breast cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Wang C, Yu Y, Zhao H, Xie L, Wang Q, Wang Y and Mu Q: MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis. Oncol Rep 46: 127, 2021.
APA
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., & Mu, Q. (2021). MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis. Oncology Reports, 46, 127. https://doi.org/10.3892/or.2021.8078
MLA
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., Mu, Q."MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis". Oncology Reports 46.1 (2021): 127.
Chicago
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., Mu, Q."MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis". Oncology Reports 46, no. 1 (2021): 127. https://doi.org/10.3892/or.2021.8078
Copy and paste a formatted citation
x
Spandidos Publications style
Wang C, Yu Y, Zhao H, Xie L, Wang Q, Wang Y and Mu Q: MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis. Oncol Rep 46: 127, 2021.
APA
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., & Mu, Q. (2021). MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis. Oncology Reports, 46, 127. https://doi.org/10.3892/or.2021.8078
MLA
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., Mu, Q."MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis". Oncology Reports 46.1 (2021): 127.
Chicago
Wang, C., Yu, Y., Zhao, H., Xie, L., Wang, Q., Wang, Y., Mu, Q."MicroRNA‑454‑5p promotes breast cancer progression by inducing epithelial‑mesenchymal transition via targeting the FoxJ2/E‑cadherin axis". Oncology Reports 46, no. 1 (2021): 127. https://doi.org/10.3892/or.2021.8078
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