STAT3 deficiency prevents hepatocarcinogenesis and promotes biliary proliferation in thioacetamide-induced liver injury

World J Gastroenterol. 2017 Oct 7;23(37):6833-6844. doi: 10.3748/wjg.v23.i37.6833.

Abstract

Aim: To elucidate the role of STAT3 in hepatocarcinogenesis and biliary ductular proliferation following chronic liver injury.

Methods: We investigated thioacetamide (TAA)-induced liver injury, compensatory hepatocyte proliferation, and hepatocellular carcinoma (HCC) development in hepatic STAT3-deficient mice. In addition, we evaluated TAA-induced biliary ductular proliferation and analyzed the activation of sex determining region Y-box9 (SOX9) and Yes-associated protein (YAP), which regulate the transdifferentiation of hepatocytes to cholangiocytes.

Results: Both compensatory hepatocyte proliferation and HCC formation were significantly decreased in hepatic STAT3-deficient mice as compared with control mice. STAT3 deficiency resulted in augmentation of hepatic necrosis and fibrosis. On the other hand, biliary ductular proliferation increased in hepatic STAT3-deficient livers as compared with control livers. SOX9 and YAP were upregulated in hepatic STAT3-deficient hepatocytes.

Conclusion: STAT3 may regulate hepatocyte proliferation as well as transdifferentiation into cholangiocytes and serve as a therapeutic target for HCC inhibition and biliary regeneration.

Keywords: Ductular reaction; Hepatocellular carcinoma; Sex determining region Y-box9; Signal transducer and activator of transcription 3; Transdifferentiation; Yes-associated protein.

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism
  • Animals
  • Biliary Tract / cytology
  • Biliary Tract / physiology*
  • Carcinogenesis / pathology*
  • Carcinoma, Hepatocellular / chemically induced
  • Carcinoma, Hepatocellular / pathology*
  • Cell Cycle Proteins
  • Cell Proliferation
  • Cell Transdifferentiation
  • Chemical and Drug Induced Liver Injury / etiology
  • Chemical and Drug Induced Liver Injury / pathology*
  • Hepatocytes / physiology
  • Liver / drug effects
  • Liver / pathology
  • Liver Neoplasms / chemically induced
  • Liver Neoplasms / pathology*
  • Liver Neoplasms, Experimental / chemically induced
  • Liver Neoplasms, Experimental / pathology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Regeneration*
  • SOX9 Transcription Factor / metabolism
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*
  • Thioacetamide / toxicity
  • Up-Regulation
  • YAP-Signaling Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins
  • Phosphoproteins
  • SOX9 Transcription Factor
  • STAT3 Transcription Factor
  • Sox9 protein, mouse
  • Stat3 protein, mouse
  • YAP-Signaling Proteins
  • Yap1 protein, mouse
  • Thioacetamide