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Article

Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression

  • Authors:
    • Cheng‑Heng Wu
    • Chau‑Ting Yeh
    • Kwang‑Huei Lin
  • View Affiliations / Copyright

    Affiliations: Department of Biochemistry, College of Medicine, Chang Gung University, Taoyuan 333, Taiwan, R.O.C., Liver Research Center, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan, R.O.C.
  • Pages: 1686-1698
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    Published online on: August 5, 2020
       https://doi.org/10.3892/or.2020.7716
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Abstract

Thyroid hormones (TH) are multifunctional mediators that fine‑tune several physiological processes, including metabolic rate, digestive function and tissue development via interactions with type II nuclear thyroid hormone receptors (TR). Upon binding of TH, TRs interact specifically with thyroid hormone response elements of target gene promoter regions to regulate their transcription. Earlier studies suggested a correlation between aberrant TR regulation and hepatocellular carcinoma (HCC). THs are involved in a crosstalk between hepatoma and stromal cells, and disruption of TH signaling is associated with tumorigenesis. Previous cDNA microarray analysis of target gene expression following T3 treatment of wild‑type TR‑expressing hepatoma cells led to the identification of forkhead box M1 (FOXM1) as a factor negatively regulated by T3 and associated with poor prognosis in several cancer types. Increased FOXM1 expression during late stages of HCC was associated with poorer overall and recurrence‑free survival in patients with HCC. However, the specific mechanisms underlying FOXM1 activity in liver cancer progression remain to be elucidated. Experiments from the present study showed that TH/TR signaling suppresses FOXM1 mRNA and protein expression. Depletion of FOXM1 induced inhibition of the cell growth rate and a decline in oncogenic cyclin D1, cyclin E and CDK2 expression. Conversely, overexpression of FOXM1 enhanced cell proliferation and expression of oncogenic factors, which was decreased upon FOXM1 depletion. Re‑expression of FOXM1 partially rescued suppression of cell proliferation induced by T3. Collectively, the present findings suggest that TH/TR participates in HCC progression via modulation of FOXM1 expression.
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Copy and paste a formatted citation
Spandidos Publications style
Wu CH, Yeh CT and Lin KH: Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression. Oncol Rep 44: 1686-1698, 2020.
APA
Wu, C., Yeh, C., & Lin, K. (2020). Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression. Oncology Reports, 44, 1686-1698. https://doi.org/10.3892/or.2020.7716
MLA
Wu, C., Yeh, C., Lin, K."Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression". Oncology Reports 44.4 (2020): 1686-1698.
Chicago
Wu, C., Yeh, C., Lin, K."Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression". Oncology Reports 44, no. 4 (2020): 1686-1698. https://doi.org/10.3892/or.2020.7716
Copy and paste a formatted citation
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Spandidos Publications style
Wu CH, Yeh CT and Lin KH: Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression. Oncol Rep 44: 1686-1698, 2020.
APA
Wu, C., Yeh, C., & Lin, K. (2020). Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression. Oncology Reports, 44, 1686-1698. https://doi.org/10.3892/or.2020.7716
MLA
Wu, C., Yeh, C., Lin, K."Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression". Oncology Reports 44.4 (2020): 1686-1698.
Chicago
Wu, C., Yeh, C., Lin, K."Thyroid hormones suppress FOXM1 expression to reduce liver cancer progression". Oncology Reports 44, no. 4 (2020): 1686-1698. https://doi.org/10.3892/or.2020.7716
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