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Article

Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro

  • Authors:
    • Jing Qiu
    • Juan Zhao
    • Anjun Zuo
    • Lan Liu
    • Qiaoqiao Liu
    • Huazheng Pan
    • Xiao Yuan
  • View Affiliations / Copyright

    Affiliations: Department of Stomatology, Qingdao Municipal Hospital, Qingdao, Shandong 266071, P.R. China, Department of Pediatrics, Jiaozhou People's Hospital, Qingdao, Shandong 266300, P.R. China, Medical Services, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China, Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China
  • Pages: 525-531
    |
    Published online on: October 2, 2018
       https://doi.org/10.3892/ol.2018.9536
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Abstract

Oral squamous cell carcinoma (OSCC) is one of the most fatal types of oral cancer worldwide. Forkhead box M1 (FOXM1) is associated with the occurrence and development of a number of types of human cancer, but its function in OSCC remains unclear. The present study aimed to explore the effect of FOXM1 downregulation using lentivirus‑mediated short hairpin (sh)RNA against FOXM1 (LV‑shFOXM1) in the cell line Tca8113 in vitro. Infection of Tca8113 cells with LV‑shFOXM1 inhibited the mRNA and protein expression level of FOXM1. The downregulation of FOXM1 resulted in cell cycle arrest of Tca8113 cells, and the inhibition of proliferation, migration and invasion. The protein expression level of cyclins B1 and D1 were downregulated, whereas those of p27 and p21 were upregulated following infection with LV‑shFOXM1, compared with the blank control and LV‑shCON groups. In addition, FOXM1 downregulation decreased the expression of matrix metalloproteinase‑2 and LV‑shFOXM1 significantly suppressed OSCC cell viability. Therefore, FOXM1 may be a target for the treatment of OSCC.
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Copy and paste a formatted citation
Spandidos Publications style
Qiu J, Zhao J, Zuo A, Liu L, Liu Q, Pan H and Yuan X: Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro. Oncol Lett 17: 525-531, 2019.
APA
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., & Yuan, X. (2019). Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro. Oncology Letters, 17, 525-531. https://doi.org/10.3892/ol.2018.9536
MLA
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., Yuan, X."Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro". Oncology Letters 17.1 (2019): 525-531.
Chicago
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., Yuan, X."Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro". Oncology Letters 17, no. 1 (2019): 525-531. https://doi.org/10.3892/ol.2018.9536
Copy and paste a formatted citation
x
Spandidos Publications style
Qiu J, Zhao J, Zuo A, Liu L, Liu Q, Pan H and Yuan X: Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro. Oncol Lett 17: 525-531, 2019.
APA
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., & Yuan, X. (2019). Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro. Oncology Letters, 17, 525-531. https://doi.org/10.3892/ol.2018.9536
MLA
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., Yuan, X."Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro". Oncology Letters 17.1 (2019): 525-531.
Chicago
Qiu, J., Zhao, J., Zuo, A., Liu, L., Liu, Q., Pan, H., Yuan, X."Lentiviral RNA interference‑mediated downregulation of Forkhead box M1 expression suppresses growth of oral squamous cell carcinoma in vitro". Oncology Letters 17, no. 1 (2019): 525-531. https://doi.org/10.3892/ol.2018.9536
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