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Endocrine-Related Cancer 14 (4) 1039 -1052     DOI: 10.1677/erc.1.01301
Copyright © 2007 by the Society for Endocrinology
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CXC chemokines located in the 4q21 region are up-regulated in breast cancer

Ivan Bièche3, Carine Chavey1,2, Catherine Andrieu3, Muriel Busson1,2, Sophie Vacher3, Ludovic Le Corre1,2, Jean-Marc Guinebretière4, Sandrine Burlinchon1,2, Rosette Lidereau3 and Gwendal Lazennec1,2

1 INSERM,, U844, Site Saint Eloi-Bat INM, 80, rue Augustin Fliche, Montpellier F-34091, France 2 University of Montpellier I,, Montpellier F-34090, France 3 INSERM,, U735, Laboratoire d'Oncogénétique and 4 Laboratoire d'Anatomo-Cytopathologie,, Centre René Huguenin, 35 rue Dailly, St-Cloud F-92211, France

(Correspondence should be addressed to G Lazennec, INSERM, U844, Site Saint Eloi-Bat INM, 80, rue Augustin Fliche, BP 74103 Montpellier Cedex 5, France; Email: lazennec{at}montp.inserm.fr)

Recent data suggest that chemokines could be essential players in breast carcinogenesis. We previously showed that the CXC chemokine CXCL8 (interleukin-8) was overexpressed in estrogen receptor {alpha} (ER{alpha})-negative breast cell lines. Analysis of CXCL8 chromosomal location showed that several CXC chemokines (CXCL1, CXCL2, CXCL3, CXCL4, CXCL4V1, CXCL5, CXCL6, CXCL7, and CXCL8) were localized in the same narrow region (360 kb in size) of chromosome 4. We thus hypothesized that they could belong to the same cluster. Quantification of these chemokines in breast tumors showed that samples expressing high CXCL8 also produced elevated levels of CXCL1, CXCL3, and CXCL5, and displayed low content of ER{alpha}. CXCL1, CXCL2, CXCL3, CXCL5, and CXCL8 were co-regulated both in tumors and in breast cancer cell lines. CXCL5 and CXCL8 were mainly produced by epithelial cells, whereas CXCL1, CXCL2, and CXCL3 had a high expression in blood cells. The overexpression of these chemokines in tumor cells was not the result of gene amplification, but rather of an enhanced gene transcription. Our data suggest that high CXCL8 expression in tumors is mainly correlated to activating protein-1 (AP-1) pathway and to a minor extent to NF-{kappa}B pathway. Interestingly, CXCL1, CXCL2, CXCL3, CXCL5, CXCL6, and CXCL8 chemokines were present at higher levels in metastases when compared with grade I and III biopsies. High levels of CXCL8, CXCL1, and CXCL3 accounted for a shorter relapse-free survival of ER{alpha}-positive patients treated with tamoxifen. In summary, we present evidences that multiple CXC chemokines are co-expressed in CXCL8-positive breast tumors. In addition, these chemokines could account for the higher aggressiveness of these types of tumors.




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