AI Article Synopsis

  • Interferon-gamma (IFN-γ) is shown to inhibit the growth of human hepatocellular carcinoma (HCC) cells (Huh7) and induces cell death without apoptosis.
  • IFN-γ promotes autophagosome formation and activates the conversion of LC3 protein, which is essential for autophagy.
  • The study highlights that IRF-1 plays a key role in mediating the autophagy induced by IFN-γ, and silencing either IRF-1, Beclin-1, or Atg5 reduces the effectiveness of IFN-γ in suppressing cell growth and promoting cell death.

Article Abstract

Interferon-gamma (IFN-γ) is a pleiotropic cytokine with immunomodulatory, anti-viral, and anti-proliferative effects. In this study, we examined the effects of IFN-γ on autophagy and cell growth in human hepatocellular carcinoma (HCC) cells. IFN-γ inhibited cell growth of Huh7 cells with non-apoptotic cell death. IFN-γ induced autophagosome formation and conversion/turnover of microtubule associated protein 1 light chain 3 (LC3) protein. Furthermore, overexpression of IRF-1 also induced autophagy in Huh7 cells. Silencing IRF-1 expression with target small hairpin RNA blocked autophagy induced by IFN-γ. Silencing of the autophagy signals Beclin-1 or Atg5 attenuated the inhibitory effect of IFN-γ on Huh7 cells with decreased cell death. Additionally, IFN-γ activated autophagy in freshly cultured human HCC cells. Together, these findings show that IFN-γ induces autophagy through IRF-1 signaling pathway and the induction of autophagy contributes to the growth-inhibitory effect of IFN-γ with cell death in human liver cancer cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3487386PMC
http://dx.doi.org/10.1016/j.canlet.2011.09.031DOI Listing

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