Recruitment of Cancer-Associated Fibroblasts and Blood Vessels by Orthotopic Liver Tumors Imaged in Red Fluorescent Protein (RFP) Transgenic Nude Mice.

Abstract

BACKGROUND/AIM:

The tumor microenvironment (TME) is critical for tumor growth and progression. We report here an imageable model of the TME of orthotopic liver cancer.

MATERIALS AND METHODS:

The transgenic red fluorescent protein (RFP)-expressing nude mouse was used as the host. The RFP nude mouse expresses RFP in all organs. Non-colored Huh-7 human hepatoma cells were injected in the spleen of RFP nude mice to establish an orthotopic liver cancer model. TME formation resulting from the orthotopic liver tumor was observed using the Olympus OV100 small animal fluorescence imaging system.

RESULTS:

Non-colored liver cancer cells formed tumor colonies in the liver 28 days after cell transplantation to the spleen. RFP-expressing host cells and blood vessels were recruited by the liver tumors as visualized by fluorescence imaging. A desmin- and sirus-red-positive area increased around and within the liver tumor over time.

CONCLUSION:

These results indicate cancer-associated fibroblasts (CAFs) were recruited by the liver tumors suggesting that CAFs, along with the angiogenic tumor blood vessels, were necessary for liver-tumor growth and could serve as visible therapeutic targets.

• Authors: Atsushi Suetsugu, Yukihiko Hiroshima, Takuro Matsumoto, Kosuke Hasagawa, Miki Nakamura, Masahito Shimizu, Shigetoyo Saji, Hisataka Moriwaki, Michael Bouvet, Robert M Hoffman
• Journal: Anticancer research (Anticancer Res) Vol. 35 Issue 11 Pg. 5821-5 (Nov 2015) ISSN: 1791-7530 [Electronic] Greece
• PMID: 26504003 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
• Copyright: Copyright© 2015 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.

Chemical References

• Luminescent Proteins
• red fluorescent protein

Topics

• Animals
• Blood Vessels (metabolism, pathology)
• Carcinoma, Hepatocellular (metabolism, pathology)
• Cells, Cultured
• Diagnostic Imaging
• Fibroblasts (metabolism, pathology)
• Humans
• Immunoenzyme Techniques
• Liver Neoplasms (metabolism, pathology)
• Luminescent Proteins (metabolism)
• Mice
• Mice, Nude
• Mice, Transgenic
• Spleen (metabolism, pathology)
• Tumor Microenvironment