## Abstract Previous studies indicated that transfection of the platelet integrin αIIbβ3 into human melanoma cells expressing integrin αvβ3 promoted their __in vivo__ (but not __in vitro__) growth and cell survival. To reveal the underlying pathomechanism, we have analyzed the angiogenic phenotype
Structure, function and biological properties of integrin αvβ3on human melanoma cells
✍ Scribed by David A. Cheresh
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 621 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0167-7659
No coin nor oath required. For personal study only.
✦ Synopsis
Human melanoma represents one of the most metastatic cancers in man. The capacity of melanoma cells to invade a variety of tissues and extracellular matrices is, in part, due to their repertoire of adhesion receptors. To this end, human melanoma cells express multiple integrin cell adhesion receptors among these is the vitronectin receptor, av[33. This adhesion receptor enables melanoma cells to attach to a wide variety of extracellular matrix components containing the sequence Arg-Gly-Asp. This review will focus on the biosynthetic, biochemical and biological properties of this receptor expressed on the surface of human melanoma cells.
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