Tumor angiogenesis after heated lipiodol infusion via the hepatic artery in a rabbit model of VX2 liver cancer

PLoS One. 2013 Apr 24;8(4):e61583. doi: 10.1371/journal.pone.0061583. Print 2013.

Abstract

Objectives: This study aimed to observe the changes in tumor angiogenesis after heated lipiodol (60°C) infusion via the hepatic artery in a rabbit model of VX2 liver cancer.

Materials and methods: Twenty rabbits with VX2 hepatic tumors were randomly divided into 2 groups (10 rabbits in each group). Under anesthesia, a trans-catheter hepatic arterial infusion was performed, and lipiodol (37°C; control group) or heated lipiodol (60°C; treated group) was injected into the hepatic arteries of the animals. Then, changes in tumor angiogenesis were assessed using the following markers and methods. 1. Vascular endothelial growth factor receptor (VEGFR) and vascular endothelial growth factor (VEGF) expression levels in the tumor were assessed using western blotting and real-time quantitative polymerase chain reaction (PCR). 2. Proliferating cell nuclear antigen (PCNA) expression in the tumor was assessed through immunohistochemical staining. 3. The morphological changes in tumor vascular endothelial cells were observed using transmission electron microscopy (TEM).

Results: VEGFR and VEGF mRNA and protein expression levels were reduced in the treated group compared to the control group. PCNA protein showed reduced expression levels in the treated group compared to the control group. TEM indicated that the endothelial cell endoplasmic reticulum expanded, the chondriosome was swollen, and the endothelial cell microvilli were decreased after heated lipiodol infusion.

Conclusions: The tumor angiogenesis of rabbits with VX2 cancer was inhibited after arterial heated lipiodol infusion compared to lipiodol infusion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiography, Digital Subtraction
  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Chemoembolization, Therapeutic
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Endothelial Cells / ultrastructure
  • Ethiodized Oil / administration & dosage*
  • Hepatic Artery
  • Liver Neoplasms, Experimental / blood supply*
  • Liver Neoplasms, Experimental / diagnosis
  • Liver Neoplasms, Experimental / therapy*
  • Male
  • Neovascularization, Pathologic / therapy*
  • Proliferating Cell Nuclear Antigen / metabolism
  • Rabbits
  • Receptors, Vascular Endothelial Growth Factor / genetics
  • Receptors, Vascular Endothelial Growth Factor / metabolism
  • Temperature
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Antineoplastic Agents
  • Proliferating Cell Nuclear Antigen
  • Vascular Endothelial Growth Factor A
  • Ethiodized Oil
  • Receptors, Vascular Endothelial Growth Factor

Grants and funding

This study was supported in part by the National Natural Science Foundation of China (No. 81170400; http://www.nsfc.gov.cn) and Shaanxi Province Science and Technology Development Projection (No.2011K13-01-16; http://www.sninfo.gov.cn). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.