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Tumor angiogenesis induced by granulocyte chemotactic protein-2 as a countercurrent principle.

Abstract
Chemokine production by tumors is a well-known phenomenon, but its role in tumor biology remains debatable. Although intratumoral injection of granulocyte chemotactic protein-2 (GCP-2) had no effect on tumor parameters, needle-free stable expression of the chemokine resulted in enhanced tumor growth. It is shown here that tumors that express a potent form of GCP-2 induce a strong influx and activation of tumor-associated neutrophils. The production of GCP-2 leads to intratumoral expression of gelatinase B and advantage for tumor growth by increased angiogenesis. These results are in line with the countercurrent principle of chemokine action and support the notion that paraneoplastic expression of ELR-positive CXC chemokines has to be blocked rather than stimulated in cancer therapy.
AuthorsE Van Coillie, I Van Aelst, A Wuyts, R Vercauteren, R Devos, C De Wolf-Peeters, J Van Damme, G Opdenakker
JournalThe American journal of pathology (Am J Pathol) Vol. 159 Issue 4 Pg. 1405-14 (Oct 2001) ISSN: 0002-9440 [Print] United States
PMID11583968 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • CXCL6 protein, human
  • Chemokine CXCL6
  • Chemokines, CXC
  • Peptide Fragments
  • Recombinant Proteins
Topics
  • Animals
  • Chemokine CXCL6
  • Chemokines, CXC (genetics, physiology)
  • Chemotaxis, Leukocyte
  • Female
  • Gene Transfer Techniques
  • Humans
  • Injections, Intralesional
  • Melanoma (blood supply, pathology, physiopathology)
  • Mice
  • Mice, Nude
  • Neoplasm Transplantation
  • Neovascularization, Pathologic (etiology)
  • Neutrophils (physiology)
  • Peptide Fragments (physiology)
  • Recombinant Proteins
  • Skin Neoplasms (blood supply, pathology, physiopathology)
  • Transfection

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