Time-dependent effect of hypoxia on tumor progression and liver progenitor cell markers in primary liver tumors

PLoS One. 2015 Mar 20;10(3):e0119555. doi: 10.1371/journal.pone.0119555. eCollection 2015.

Abstract

Background & aims: Expression of liver progenitor cell (LPC) characteristics has been proposed as a negative prognostic marker in primary liver tumors. Hypoxia has been linked to activation of the Notch pathway which is responsible for activation and proliferation of LPCs and hypoxia-induced LPC activation has been shown in hepatocellular carcinoma. Our aim was to elucidate the time-dependent effects of hypoxia on the LPC niche in hepatocellular carcinoma which could aid in determining a safe time frame for use of hypoxia inducing therapies.

Methods: We used dimethyloxaloylglycine to mimic a hypoxic reaction in mice by stabilizing hypoxia-inducible factor 1 alpha at three distinct time points in diethylnitrosamine induced hepatocarcinogenesis. LPC, metastasis and Notch pathway markers were determined by quantitative PCR and (immune)histochemistry (heamatoxillin-eosin, reticulin, Sirius red and cytokeratin 19 staining).

Results: Activating the hypoxia inducible pathway early in hepatocarcinogenesis resulted in an increased incidence of both cholangioma and hepatocellular lesions, associated with high expression of LPC, metastatic and Notch pathway markers. Adversely, activating the hypoxic response during tumor development resulted in decreased incidence of hepatocellular lesions and increased cholangioma incidence, with an unaltered gene expression profile of LPC-, Notch pathway- and metastatic markers. A hypoxic insult at advanced stages of hepatocarcinogenesis severely increased the expression of LPC characteristics, however without increased expression of actors of the Notch pathway and metastatic markers and minor changes in incidence of hepatocellular and cholangioma lesions.

Conclusion: Our results indicate that increased hypoxia at the onset of tumor development has detrimental effects on tumor progression; patients with HCC developed in a background of fibrosis/cirrhosis might therefore represent a more difficult treatment group. In contrast, hypoxia during tumor development appears to favor tumor outcome, highlighting the importance of early detection. Finally, hypoxia in advanced stages resulted in increased expression of LPC characteristics indicating poor outcome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Neoplasm / metabolism
  • Biomarkers
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / metabolism*
  • Carcinoma, Hepatocellular / pathology*
  • Cell Adhesion Molecules / metabolism
  • Cell Transformation, Neoplastic / chemically induced
  • Cell Transformation, Neoplastic / genetics
  • Cell Transformation, Neoplastic / metabolism
  • Disease Models, Animal
  • Disease Progression
  • Epithelial Cell Adhesion Molecule
  • Gene Expression
  • Hypoxia / metabolism*
  • Hypoxia-Inducible Factor 1, alpha Subunit / genetics
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Immunohistochemistry
  • Keratin-19 / metabolism
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism*
  • Liver Neoplasms / pathology*
  • Male
  • Mice
  • Neoplasm Metastasis
  • RNA, Messenger / genetics
  • Receptors, Notch / metabolism
  • Stem Cells / metabolism*
  • Time Factors

Substances

  • Antigens, Neoplasm
  • Biomarkers
  • Cell Adhesion Molecules
  • Epithelial Cell Adhesion Molecule
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Keratin-19
  • RNA, Messenger
  • Receptors, Notch

Grants and funding

This study was supported by the research foundation Flanders (FWO) project (G033313N) and Xavier Verhelst and Hans Van Vlierberghe are clinical investigators for the research foundation Flanders (FWO) (www.FWO.be). Eliene Bogaerts was funded by an "Emmanuel van der Schueren" grant by the flemmish league against cancer (VLK). Femke Heindryckx received funding from the Wenner-Gren Foundation—Sweden. Lindsey Devisscher and Yves-Paul Vandewynckel are supported by a grant of the special research fund (BOF) from Ghent University (01D20510 and B/12531/01) (www.UGent.be). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.