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Papers In Press, published online ahead of print April 26, 2002
Molecular Immunology, Rega Institute for Medical Research, KULeuven, Leuven B-3000
Corresponding Author: jozef.vandamme{at}rega.kuleuven.ac.be
Chemokines are important in leukocyte homeostasis, inflammation, angiogenesis and metastasis. Here, the molecular diversity of chemokines present in ovarian carcinoma was studied by purifying the proteins to homogeneity from ascitic fluid. Biologically active intact CCL2 and processed CXCL8, CCL3 and CCL18 isoforms were recovered. CCL7 and CCL20 were also purified but their levels were 10-fold lower compared to CXCL8, CCL2 and CCL3, and even 100-fold lower than the amounts of CCL18 isolated. In ascitic fluids from patients with ovarian carcinoma (n=12), significantly higher levels of CXCL8 and CCL18 (respectively 2.0 ng/ml versus 0.7 ng/ml, p=0.01 and 120 ng/ml versus 44 ng/ml, p=0.0002) were detected compared to those in non-ovarian carcinoma patients (n=12). In contrast to CXCL8, CCL18 was not inducible in carcinoma cell lines. Immunostaining showed CCL18 expression in tumor-infiltrating cells with monocyte/macrophage morphology but not in the ovarian carcinoma cells. Our data demonstrate that biochemically heterogenous, but biologically active forms of several chemokines are present at different concentrations in ovarian carcinoma ascitic fluid. This points to a delicate balance of chemokines in epithelial ovarian cancer and to a potentially major role for CXCL8 and CCL18 in this tumor.
J. Biol. Chem, 10.1074/jbc.M112275200
Submitted on December 21, 2001
Revised on April 25, 2002
Accepted on April 26, 2002
Identification of biologically active chemokine isoforms from ascitic fluid and elevated levels of CCL18/Pulmonary and activation-regulated chemokine in ovarian carcinoma
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