Journal Article

Role of ICAM1 in invasion of human breast cancer cells

Caridad Rosette, Richard B. Roth, Paul Oeth, Andreas Braun, Stefan Kammerer, Jonas Ekblom and Mikhail F. Denissenko

in Carcinogenesis

Volume 26, issue 5, pages 943-950
Published in print May 2005 | ISSN: 0143-3334
Published online March 2005 | e-ISSN: 1460-2180 | DOI:
Role of ICAM1 in invasion of human breast cancer cells

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We identified previously a region on chromosome 19p13.2 spanning the genes encoding the intercellular adhesion molecules (ICAM), ICAM1, ICAM4 and ICAM5 as a breast cancer susceptibility locus. Genetic variants in this region were also associated with indicators of disease severity, including higher rates of metastases to other organs. Based on this association, we set out to explore the role of ICAM1 in proliferation and invasion of human breast cancer cells. We observed that ICAM1 downregulation at the mRNA and protein levels led to a strong suppression of human breast cell invasion through a matrigel matrix. Under the same conditions, no significant effect on cell proliferation in vitro was seen. Incubation of cells with an antibody against ICAM1 blocked invasion of the highly metastatic MDA-MB-435 cell line in a dose-dependent manner without affecting cell migration. We also demonstrated that the level of ICAM1 protein expression on the cell surface positively correlated with metastatic potential of five human breast cancer cell lines and that ICAM1 mRNA levels were elevated in breast tumor compared with adjacent normal tissue. These results corroborate our previous genetic finding that variations in the ICAM region are associated with the occurrence of metastases and establish a causal role of ICAM1 in invasion of metastatic human breast carcinoma cell lines.

Keywords: ICAM1, intercellular adhesion molecule 1; MALDI-TOF MS, matrix-assisted laser desorption-ionization time-of-flight mass spectrometry; MUC1, mucin 1; QGE, quantitative gene expression; siRNA, small-interfering RNA

Journal Article.  5465 words.  Illustrated.

Subjects: Clinical Cytogenetics and Molecular Genetics

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