Thromb Haemost 2003; 90(04): 591-597
DOI: 10.1160/TH03-04-0206
Review Article
Schattauer GmbH

Lymphangiogenesis and tumor metastasis

Riccardo E. Nisato
1   Department of Morphology, University Medical Center, Geneva, Switzerland
,
Jean-Christophe Tille
1   Department of Morphology, University Medical Center, Geneva, Switzerland
,
Michael S. Pepper
1   Department of Morphology, University Medical Center, Geneva, Switzerland
› Author Affiliations
Further Information

Publication History

Received 02 April 2003

Accepted after resubmission 27 July 2003

Publication Date:
05 December 2017 (online)

Summary

In several human cancers, increased expression in primary tumors of vascular endothelial growth factor-C (VEGF-C) is correlated with regional lymph node metastasis. Studies using transgenic mice overexpressing VEGF-C, or xenotransplantation of VEGF-C-expressing tumor cells into immunodeficient mice, have demonstrated a role for VEGF-C in tumor lymphangiogenesis and the subsequent formation of lymph node metastasis. However, at variance with data obtained in animal models, there is at present very little evidence for lymphangiogenesis in human tumors. Nonetheless, the striking correlation between levels of VEGF-C in primary human tumors and lymph node metastases exists, which suggests that VEGF-C may serve functions other than lymphangiogenesis. Thus, VEGF-C may activate pre-existing lymphatics which in turn become directly involved in tumor cell chemotaxis, intralymphatic intravasation and distal dissemination. A reciprocal dialogue is therefore likely to exist between tumor and lymphatic endothelial cells which results in the formation of lymph node metastases.

This publication was partially financed by Serono Foundation for the Advancement of Medical Science.

Part of this paper was originally presented at the 2nd International Workshop on New Therapeutic Targets in Vascular Biology from February 6-9, 2003 in Geneva, Switzerland.

 
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