Metformin inhibits the prometastatic effect of sorafenib in hepatocellular carcinoma by upregulating the expression of TIP30

Cancer Sci. 2016 Apr;107(4):507-13. doi: 10.1111/cas.12885. Epub 2016 Feb 23.

Abstract

We previously found that a low dose of sorafenib had a prometastatic effect on hepatocellular carcinoma (HCC), which was caused by downregulation of TIP30 expression. More recently, metformin has been shown to have potential as a preventive and therapeutic agent for different cancers, including HCC. This study evaluated whether the combination of sorafenib and metformin is sufficient to revert the expression of TIP30, thereby simultaneously reducing lung metastasis and improving survival. Our data show that the combination of sorafenib and metformin inhibits proliferation and invasion in vitro, prolongs median survival, and reduces lung metastasis of HCC in vivo. This effect is closely associated with the upregulation of TIP30, partly through activating AMP-activated protein kinase. Thioredoxin, a prometastasis factor, is negatively regulated by TIP30 and plays an essential role during the process of HCC metastasis. Overall, our results suggest that metformin might be a potent enhancer for the treatment of HCC by using sorafenib.

Keywords: Hepatocellular carcinoma; human TIP30 protein; metformin; sorafenib; thioredoxins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyltransferases / biosynthesis*
  • Acetyltransferases / genetics
  • Animals
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / pathology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / genetics
  • Liver Neoplasms / pathology
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Lung Neoplasms / secondary
  • Metformin / administration & dosage*
  • Mice
  • Neoplasm Invasiveness / genetics
  • Neoplasm Metastasis
  • Niacinamide / administration & dosage
  • Niacinamide / adverse effects
  • Niacinamide / analogs & derivatives
  • Phenylurea Compounds / administration & dosage
  • Phenylurea Compounds / adverse effects
  • Signal Transduction
  • Sorafenib
  • Thioredoxins / genetics
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Xenograft Model Antitumor Assays

Substances

  • Phenylurea Compounds
  • Transcription Factors
  • Niacinamide
  • Thioredoxins
  • Metformin
  • Sorafenib
  • Acetyltransferases
  • HTATIP2 protein, human