Function and mechanism by which interferon regulatory factor‑1 inhibits oncogenesis (Review)

  • Authors:
    • Fei‑Fei Chen
    • Guan Jiang
    • Kerui Xu
    • Jun‑Nian Zheng
  • View Affiliations

  • Published online on: November 28, 2012     https://doi.org/10.3892/ol.2012.1051
  • Pages: 417-423
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Abstract

The present review focuses on recent advances in the understanding of the molecular mechnisms by which interferon regulatory factor (IRF)‑1 inhibits oncogenesis. IRF‑1 is associated with regulation of interferon α and β transcription. In addition, numerous clinical studies have indicated that IRF‑1 gene deletion or rearrangement correlates with development of specific forms of human cancer. IRF‑1 has been revealed to exhibit marked functional diversity in the regulation of oncogenesis. IRF‑1 activates a set of target genes associated with regulation of the cell cycle, apoptosis and the immune response. The role of IRF‑1 in the regulation of various types of human tumor has important implications for understanding the susceptibility and progression of cancer. In addition, an improved understanding of the role of IRF‑1 in the pathological processes that lead to human malignant diseases may aid development of novel therapeutic strategies.
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February 2013
Volume 5 Issue 2

Print ISSN: 1792-1074
Online ISSN:1792-1082

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Spandidos Publications style
Chen FF, Jiang G, Xu K and Zheng JN: Function and mechanism by which interferon regulatory factor‑1 inhibits oncogenesis (Review). Oncol Lett 5: 417-423, 2013.
APA
Chen, F., Jiang, G., Xu, K., & Zheng, J. (2013). Function and mechanism by which interferon regulatory factor‑1 inhibits oncogenesis (Review). Oncology Letters, 5, 417-423. https://doi.org/10.3892/ol.2012.1051
MLA
Chen, F., Jiang, G., Xu, K., Zheng, J."Function and mechanism by which interferon regulatory factor‑1 inhibits oncogenesis (Review)". Oncology Letters 5.2 (2013): 417-423.
Chicago
Chen, F., Jiang, G., Xu, K., Zheng, J."Function and mechanism by which interferon regulatory factor‑1 inhibits oncogenesis (Review)". Oncology Letters 5, no. 2 (2013): 417-423. https://doi.org/10.3892/ol.2012.1051