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Publication Date:
May 2008
ISSN:
1437-4315
DOI:
10.1515/BC.2008.088

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Gene expression changes associated with the anti-angiogenic activity of kallikrein-related peptidase 3 (KLK3) on human umbilical vein endothelial cells

Johanna M. Mattsson1 / Pirjo Laakkonen2 / Sami Kilpinen3 / Ulf-Håkan Stenman4 / Hannu Koistinen5

1Department of Clinical Chemistry, Biomedicum Helsinki, University of Helsinki and Helsinki University Central Hospital, 00014 University of Helsinki, Finland

2Molecular Cancer Biology Research Program and Institute of Biomedicine, Biomedicum Helsinki, University of Helsinki, 00014 University of Helsinki, Finland

3Medical Biotechnology, VTT Technical Research Center and University of Turku, 20520 Turku, Finland, and Genome-Scale Biology Research Program, Biomedicum Helsinki, 00014 University of Helsinki, Finland

4Department of Clinical Chemistry, Biomedicum Helsinki, University of Helsinki and Helsinki University Central Hospital, 00014 University of Helsinki, Finland

5Department of Clinical Chemistry, Biomedicum Helsinki, University of Helsinki and Helsinki University Central Hospital, 00014 University of Helsinki, Finland

Corresponding author

Citation Information: Biological Chemistry. Volume 389, Issue 6, Pages 765–771, ISSN (Online) 14374315, ISSN (Print) 1431-6730, DOI: 10.1515/BC.2008.088, May 2008

Publication History:
Received:
2007-12-14
Accepted:
2008-03-10
Published Online:
2008-05-15

Abstract

Kallikrein-related peptidase 3 (KLK3, also known as prostate-specific antigen, PSA) is a chymotrypsin-like kallikrein that has anti-angiogenic properties. We have previously shown in a human umbilical vein endothelial cell (HUVEC) model that the anti-angiogenic effect of KLK3 is related to its enzyme activity. However, the mechanism of this effect remains to be clarified. To this end, we used a DNA microarray to study KLK3-induced changes in gene expression associated with reduction of HUVEC tube formation. Among the 41 000 genes studied, 311 were differentially expressed between control and KLK3-treated cells. These changes were enriched in several pathways, including those associated with proteasome, ubiquitin-mediated proteolysis, focal adhesion and regulation of the actin cytoskeleton. Furthermore, the changes were opposite to those previously described to occur during tubulogenesis. In conclusion, our results show that KLK3 induces gene expression changes in HUVECs. Although these changes might be relevant for the mechanism by which KLK3 exerts its anti-angiogenic activity, it cannot be judged from the present results whether they reflect the primary mechanism mediating the effect of KLK3 or are secondary to morphogenic differentiation.

Keywords: angiogenesis; cell culture; microarray; prostate cancer; PSA

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