## Abstract Cell interaction with the extracellular matrix (ECM) has profound influence in cancer progression. The __s__ecreted __p__rotein, __a__cidic and __r__ich in __c__ysteine (SPARC) a component of the ECM, impairs the proliferation of different cell types and modulates tumor cell aggressive
Extracellular matrix modulates the function of human melanocytes but not melanoma cells
โ Scribed by Marie Ranson; Solomon Posen; Rebecca S. Mason
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 872 KB
- Volume
- 136
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
โฆ Synopsis
Normal human epidermal melanocytes are attached to a basement membrane, a specialized form of extracellular matrix (ECM), located between the epithelium and underlying dermal tissues. To determine whether ECM influences pigmented cell behavior in vitro, human epidermal rnelanocytes and melanoma cells were cultured on uncoated or ECM-coated plastic culture surfaces, and a comparison was made between growth and function in the presence or absence of ECM. Melanocytes cultured on ECM-coated surfaces developed flatter and larger cell bodies and produced more melanin than melanocytes cultured on uncoated surfaces. In the presence of phorbol-myristate-acetate and cholera toxin, the rate of melanocyte replication was increased by ECM. In the absence of these mitogens, ECM significantly enhanced the adhesiveness of nonproliferating melanocytes. ECM had little or no effect on these parameters (morphology, tyrosinase activity, replication) in a pigmented human malignant melanoma cell line. These findings indicate that normal human epidermal pigment cells have the ability to recognize and respond to matrix signals, whereas this capacity appears to be absent in melanoma cells.
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