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Published in: Molecular Cancer 1/2011

Open Access 01-12-2011 | Research

A MCP1 fusokine with CCR2-specific tumoricidal activity

Authors: Moutih Rafei, Jiusheng Deng, Marie-Noëlle Boivin, Patrick Williams, Shannon M Matulis, Shala Yuan, Elena Birman, Kathy Forner, Liangping Yuan, Craig Castellino, Lawrence H Boise, Tobey J MacDonald, Jacques Galipeau

Published in: Molecular Cancer | Issue 1/2011

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Abstract

Background

The CCL2 chemokine is involved in promoting cancer angiogenesis, proliferation and metastasis by malignancies that express CCR2 receptor. Thus the CCL2/CCR2 axis is an attractive molecular target for anticancer drug development.

Methods

We have generated a novel fusion protein using GMCSF and an N-terminal truncated version of MCP1/CCL2 (6-76) [hereafter GMME1] and investigated its utility as a CCR2-specific tumoricidal agent.

Results

We found that distinct to full length CCL2 or its N-truncated derivative (CCL2 5-76), GMME1 bound to CCR2 on mouse lymphoma EG7, human multiple myeloma cell line U266, or murine and human medulloblastoma cell lines, and led to their death by apoptosis. We demonstrated that GMME1 specifically blocked CCR2-associated STAT3 phosphorylation and up-regulated pro-apoptotic BAX. Furthermore, GMME1 significantly inhibited EG7 tumor growth in C57BL/6 mice, and induced apoptosis of primary myeloma cells from patients.

Conclusion

Our data demonstrate that GMME1 is a fusokine with a potent, CCR2 receptor-mediated pro-apoptotic effect on tumor cells and could be exploited as a novel biological therapy for CCR2+ malignancies including lymphoid and central nervous system malignancies.
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Metadata
Title
A MCP1 fusokine with CCR2-specific tumoricidal activity
Authors
Moutih Rafei
Jiusheng Deng
Marie-Noëlle Boivin
Patrick Williams
Shannon M Matulis
Shala Yuan
Elena Birman
Kathy Forner
Liangping Yuan
Craig Castellino
Lawrence H Boise
Tobey J MacDonald
Jacques Galipeau
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Molecular Cancer / Issue 1/2011
Electronic ISSN: 1476-4598
DOI
https://doi.org/10.1186/1476-4598-10-121

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