Tumor endothelial cells express high pentraxin 3 levels

Pathol Int. 2016 Dec;66(12):687-694. doi: 10.1111/pin.12474. Epub 2016 Nov 14.

Abstract

It has been described that tumor progression has many similarities to inflammation and wound healing in terms of the signaling processes involved. Among biological responses, angiogenesis, which is necessary for tumor progression and metastasis, is a common hallmark; therefore, tumor blood vessels have been considered as important therapeutic targets in anticancer therapy. We focused on pentraxin 3 (PTX3), which is a marker of cancer-related inflammation, but we found no reports on its expression and function in tumor blood vessels. Here we showed that PTX3 is expressed in mouse and human tumor blood vessels based on immunohistochemical analysis. We found that PTX3 is upregulated in primary mouse and human tumor endothelial cells compared to normal endothelial cells. We also showed that PTX3 plays an important role in the proliferation of the tumor endothelial cells. These results suggest that PTX3 is an important target for antiangiogenic therapy.

Keywords: angiogenesis; antiangiogenic drugs; cancer; pentraxin 3; tumor endothelial cells.

MeSH terms

  • Animals
  • Blood Vessels / physiopathology
  • C-Reactive Protein / genetics*
  • C-Reactive Protein / metabolism
  • Cell Proliferation / genetics
  • Endothelial Cells / pathology*
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Mice
  • Neoplasms / physiopathology*
  • Serum Amyloid P-Component / genetics*
  • Serum Amyloid P-Component / metabolism

Substances

  • Serum Amyloid P-Component
  • PTX3 protein
  • C-Reactive Protein