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Updated: Feb 22, 2026

Murine Model of Metastatic Liver Tumors in the Setting of Ischemia Reperfusion Injury
Published on: August 30, 2019
Role of liver ICAM-1 in metastasis
Aitor Benedicto1, Irene Romayor1, Beatriz Arteta1
1Department of Cell Biology and Histology, School of Medicine and Nursing, University of The Basque Country, UPV/EHU, Leioa, E-48940 Vizcaya, Spain.
Insights
Intercellular adhesion molecule (ICAM)-1, a protein found on liver cells, may play a key role in cancer metastasis to the liver. Further research into ICAM-1 mechanisms could lead to new cancer therapies.
Area of Science:
- Immunology
- Oncology
- Cell Biology
Background:
- Intercellular adhesion molecule (ICAM)-1 is a transmembrane glycoprotein involved in physiological processes and expressed in various cancer cells.
- While ICAM-1 expression on tumor cells is studied, its role at metastatic sites, particularly the liver, is less understood.
- The liver's unique physiology and sinusoidal network make it a common site for cancer metastasis.
Purpose of the Study:
- To investigate the role of ICAM-1 in liver metastasis.
- To enhance understanding of ICAM-1-mediated mechanisms in cancer spread to the liver.
- To explore potential host-directed anticancer therapies targeting ICAM-1.
Main Methods:
- The study focuses on the expression and potential role of ICAM-1 in the context of liver metastasis.
- It reviews existing literature on ICAM-1 expression in various cancers and its presence on liver sinusoidal endothelial cells.
- The research highlights the need for further investigation into ICAM-1's function in metastatic development.
Main Results:
- Liver sinusoidal endothelial cells constitutively express ICAM-1, with upregulation under inflammatory conditions.
- ICAM-1 expression on liver cells may be significant in the development of liver metastasis.
- Current research primarily focuses on ICAM-1 on tumor cells, not at metastatic sites.
Conclusions:
- Understanding ICAM-1's role in liver metastasis is crucial for developing targeted therapies.
- Further research is needed to elucidate the specific mechanisms by which ICAM-1 influences cancer cell adhesion and extravasation in the liver.
- Targeting ICAM-1 could represent a novel strategy for host-directed anticancer treatments against liver metastases.
Abstract:
Intercellular adhesion molecule (ICAM)-1, is a transmembrane glycoprotein of the immunoglobulin (Ig)-like superfamily, consisting of five extracellular Ig-like domains, a transmembrane domain and a short cytoplasmic tail. ICAM-1 is expressed in various cell types, including endothelial cells and leukocytes, and is involved in several physiological processes. Furthermore, it has additionally been reported to be expressed in various cancer cells, including melanoma, colorectal cancer and lymphoma. The majority of studies to date have focused on the expression of the ICAM-1 on the surface of tumor cells, without research into ICAM-1 expression at sites of metastasis. Cancer cells frequently metastasize to the liver, due to its unique physiology and specialized liver sinusoid capillary network. Liver sinusoidal endothelial cells constitutively express ICAM-1, which is upregulated under inflammatory conditions. Furthermore, liver ICAM-1 may be important during the development of liver metastasis. Therefore, it is necessary to improve the understanding of the mechanisms mediated by this adhesion molecule in order to develop host-directed anticancer therapies.
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