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Updated: Aug 10, 2026

Experimental Metastasis Assay
Published on: August 25, 2010
Soluble intercellular adhesion molecule 1 is released by human melanoma cells and is associated with tumor growth in
R Giavazzi1, R G Chirivi, A Garofalo
1Mario Negri Institute for Pharmacological Research, Bergamo, Italy.
Insights
Cytokines like TNF and IL-1 boost cell surface Intercellular Adhesion Molecule 1 (ICAM-1) on melanoma cells. These cytokines also trigger soluble ICAM-1 release, potentially linking tumor immunity to elevated ICAM-1 in patients.
Area of Science:
- Immunology
- Cell Biology
- Oncology
Background:
- Intercellular Adhesion Molecule 1 (ICAM-1) plays a role in immune responses.
- Elevated soluble ICAM-1 is observed in melanoma patients, but its source is unclear.
- Melanoma cell lines offer a model to study ICAM-1 regulation.
Purpose of the Study:
- To investigate how cytokines regulate ICAM-1 expression on human melanoma cells.
- To determine if melanoma tumors release soluble ICAM-1 in vivo.
- To explore the potential source of elevated soluble ICAM-1 in melanoma patients.
Main Methods:
- Utilized the human melanoma cell line A375M.
- Treated cells with cytokines including Interleukin 1 (IL-1), Interleukin 6 (IL-6), Tumor Necrosis Factor (TNF), and gamma-interferon (IFN-γ).
- Measured cell surface and soluble ICAM-1 levels; analyzed serum from tumor-bearing mice.
Main Results:
- Unstimulated A375M cells expressed cell surface ICAM-1 but minimal soluble ICAM-1.
- IL-1, IL-6, TNF, and IFN-γ increased cell surface ICAM-1 expression.
- TNF, IL-1, and IFN-γ induced the release of soluble ICAM-1.
- Soluble human ICAM-1 was detected in serum from mice bearing human melanoma tumors, correlating positively with tumor weight.
Conclusions:
- Cytokines significantly regulate both cell surface and soluble ICAM-1 expression in melanoma cells.
- Melanoma tumors can be a source of soluble ICAM-1.
- Cytokine-induced release of ICAM-1 from tumors may be relevant to immune recognition in melanoma.
Abstract:
We have studied the cytokine regulation of cell surface and soluble intercellular adhesion molecule 1 (ICAM-1) expression on the human melanoma cell line A375M. Unstimulated cells express ICAM-1 on their cell surface but do not secrete significant levels of soluble ICAM-1. Interleukin 1, interleukin 6, tumor necrosis factor, and gamma-interferon all increased cell surface expression of ICAM-1. Tumor necrosis factor, interleukin 1, and gamma-interferon also caused the release of soluble ICAM-1. The serum of melanoma patients has been reported to contain elevated levels of soluble ICAM-1; however, the source of this ICAM-1 is unclear. The serum from nude mice bearing s.c. human melanoma tumors was found to contain soluble human ICAM-1. ICAM-1 levels showed a positive correlation with tumor weight. The release of ICAM-1 from melanoma tumors, in response to host-derived cytokines, may have relevance to immune recognition of the tumor.
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