Leflunomide inhibits proliferation and tumorigenesis of oral squamous cell carcinoma

  • Authors:
    • Aishu Ren
    • Gang Fu
    • Yu Qiu
    • Hongjuan Cui
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  • Published online on: October 10, 2017     https://doi.org/10.3892/mmr.2017.7755
  • Pages: 9125-9130
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Abstract

Oral squamous cell carcinoma (OSCC) is the most prevalent pathological cancer occurring in the head and neck area. Progress has previously been made regarding treatment strategies of OSCC, however the 5‑year survival rate of these patients is only 50%. The present study examined if leflunomide (LEF), a drug primarily used for the treatment of rheumatoid arthritis, exhibited antitumor effects in OSCC. The results demonstrated that LEF inhibited cell proliferation and blocked the cell cycle at the S phase in OSCC cells, with upregulation of cyclin A protein expression. LEF reduced the expression of dihydroorotate dehydrogenase, which is an essential enzyme in the de novo pyrimidine biosynthetic pathway. LEF additionally inhibited colony formation in soft agar and reduced tumor growth in a xenograft model. The results suggested that LEF may act as a potential therapeutic agent in the treatment of OSCC in the future.
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December-2017
Volume 16 Issue 6

Print ISSN: 1791-2997
Online ISSN:1791-3004

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Spandidos Publications style
Ren A, Fu G, Qiu Y and Cui H: Leflunomide inhibits proliferation and tumorigenesis of oral squamous cell carcinoma. Mol Med Rep 16: 9125-9130, 2017
APA
Ren, A., Fu, G., Qiu, Y., & Cui, H. (2017). Leflunomide inhibits proliferation and tumorigenesis of oral squamous cell carcinoma. Molecular Medicine Reports, 16, 9125-9130. https://doi.org/10.3892/mmr.2017.7755
MLA
Ren, A., Fu, G., Qiu, Y., Cui, H."Leflunomide inhibits proliferation and tumorigenesis of oral squamous cell carcinoma". Molecular Medicine Reports 16.6 (2017): 9125-9130.
Chicago
Ren, A., Fu, G., Qiu, Y., Cui, H."Leflunomide inhibits proliferation and tumorigenesis of oral squamous cell carcinoma". Molecular Medicine Reports 16, no. 6 (2017): 9125-9130. https://doi.org/10.3892/mmr.2017.7755