Thrombin receptor overexpression in malignant and physiological invasion processes
- 1 August 1998
- journal article
- research article
- Published by Springer Nature in Nature Medicine
- Vol. 4 (8) , 909-914
- https://doi.org/10.1038/nm0898-909
Abstract
Although the involvement of soluble and matrix-immobilized proteases in tumor cell invasion and metastasis is well recognized, the role of proteolytically activated cell surface receptors has not been elucidated. We report here that thrombin receptor, a member of the protease-activated receptor family, is preferentially expressed in highly metastatic human breast carcinoma cell lines and breast carcinoma biopsy specimens. Introduction of thrombin receptor antisense cDNA considerably inhibited the invasion of metastatic breast carcinoma cells in culture through a reconstituted basement membrane. During placental implantation of the human embryo, thrombin receptor is transiently expressed in the invading cytotrophoblasts. These results emphasize the involvement of thrombin receptor in cell invasion associated with tumor progression and normal embryonic development.Keywords
This publication has 39 references indexed in Scilit:
- Thrombin Receptor-Mediated Increase of Two Matrix Metalloproteinases, MMP-1 and MMP-3, in Human Endothelial CellsArteriosclerosis, Thrombosis, and Vascular Biology, 1997
- The Configuration of Fibrin Clots Determines Capillary Morphogenesis and Endothelial Cell MigrationMicrovascular Research, 1996
- Molecular Cloning and Functional Expression of the Gene Encoding the Human Proteinase‐Activated Receptor 2European Journal of Biochemistry, 1995
- Specificity of the thrombin receptor for agonist peptide is defined by its extracellular surfaceNature, 1994
- Thrombin increases the metastatic potential of tumor cellsInternational Journal of Cancer, 1993
- Invasion of the trophoblastsCell, 1992
- Why do cancer cells metastasize into particular organs?BioEssays, 1992
- Duct carcinoma in situ: 227 cases without microinvasionEuropean Journal Of Cancer, 1992
- Molecular cloning of a functional thrombin receptor reveals a novel proteolytic mechanism of receptor activationCell, 1991
- The Cellular Basis of Site-Specific Tumor MetastasisNew England Journal of Medicine, 1990