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PMID: 7704939 Published · ppublish English Journal Article

Mechanisms involved in metastasis enhanced by inflammatory mediators.

Circulatory shock ·Vol. 44 ·No. 1 ·1994-09-00 ·Pages 9-13

Männel DN, Orosz P, Hafner M, Falk W

Abstract

The enhancement of tumor metastasis by concurrent inflammatory processes is mainly due to the cytokines TNF and IL-1. In the case of TNF this effect is not restricted to metastasis models as measured by in vivo colony formation but also found in experimental model systems of spontaneous metastasis. Direct effects on the tumor cells or interference with the host NK cell system did not seem to account for the observed TNF effect. Experimental evidence from different test systems rather points to TNF- or IL-1-induced enhanced adhesion of tumor cells to the endothelial cell layer as the underlying mechanism. Blocking of integrin-matrix interactions with monoclonal antibodies or competing peptides inhibited tumor cell adhesion to endothelioma cells in vitro and lung colony formation of tumor cells in vivo.

MeSH Terms
Animals Cell Adhesion Endothelium, Vascular/pathology Female Fibrosarcoma/pathology Humans Inflammation/complications Interleukin-1/pharmacology Killer Cells, Natural/physiology Lymphoma/pathology Mice Mice, Inbred C57BL Neoplasm Metastasis Recombinant Proteins/pharmacology Tumor Necrosis Factor-alpha/pharmacology
Chemicals
Interleukin-1 Recombinant Proteins Tumor Necrosis Factor-alpha
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Männel D N
Department of Pathology, University of Regensburg, Germany.
Orosz P
Hafner M
Falk W
Article Info
Journal
Circulatory shock
Abbr.
Circ Shock
ISSN
0092-6213
Published
1994-09-00
Pages
9-13
Language
English
Region
United States
NLM ID
0414112
Subset
IM
External Links
PubMed source
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