Hepatitis B virus X protein induces expression of alpha-fetoprotein and activates PI3K/mTOR signaling pathway in liver cells

Oncotarget. 2015 May 20;6(14):12196-208. doi: 10.18632/oncotarget.2906.

Abstract

The hepatitis B virus (HBV)-X protein (HBx) induces malignant transformation of liver cells, and elevated expression of alpha-fetoprotein (AFP) is a significant biomarker of hepatocarcinogenesis. However, the role of AFP in HBV-related hepatocarcinogenesis is unclear. In this study, we investigated the regulatory impact of AFP expression on HBx-mediated malignant transformation of human hepatocytes. We found that HBV induced the expression of AFP before that of oncogenes, e.g., Src, Ras and chemokine (C-X-C motif) receptor 4 (CXCR4), and AFP activated protein kinase B (AKT) and mammalian target of rapamycin (mTOR) in HBV-related HCC tissues and in human liver cells transfected with HBx. Cytoplasmic AFP interacted with and inhibited phosphatase and tensin homolog deleted on chromosome 10 (PTEN), activating the phosphatidylinositol 3-kinase (PI3K)/AKT signaling pathway and promoting mTOR-mediated stimulation of the transcription factor hypoxia inducible factor-1α (HIF-1α), and therefore led to the activation of the promoters of Src, CXCR4, and Ras genes. On the contrary, reduced expression of AFP by siRNA resulted in the repression of p-mTOR, pAKT, Src, CXCR4, and Ras in human malignant liver cells. Taken together, for the first time our study indicates that HBx-induced AFP expression critically promote malignant transformation in liver cells through the activation of PI3K/mTOR signaling.

Keywords: AFP; HBx; PI3K/mTOR signaling; hepatocarcinogenesis; liver cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Humans
  • Liver / metabolism*
  • Phosphatidylinositol 3-Kinase / metabolism*
  • Phosphorylation
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism*
  • Trans-Activators / genetics*
  • Trans-Activators / metabolism*
  • Transfection
  • Viral Regulatory and Accessory Proteins
  • alpha-Fetoproteins / metabolism*

Substances

  • Trans-Activators
  • Viral Regulatory and Accessory Proteins
  • alpha-Fetoproteins
  • hepatitis B virus X protein
  • MTOR protein, human
  • Phosphatidylinositol 3-Kinase
  • TOR Serine-Threonine Kinases