This is a report from the Kananaskis working group on quantitative methods in tumour heterogeneity. Tumour progression is currently believed to result from genetic instability and consequent acquisition of new genetic properties in some of the tumour cells. Cross-sectional assessment of genetic mark
Markers of melanocytic tumour progression
โ Scribed by Ruiter, Dirk J.; Van Muijen, Goos N. P.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 159 KB
- Volume
- 186
- Category
- Article
- ISSN
- 0022-3417
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โฆ Synopsis
Melanoma progression markers can be defined as molecules with a preferential expression in one or a few stages of melanocytic tumour development. These molecules include growth factors, growth factor receptors, adhesion molecules, proteases and related components. Immunohistochemical studies suggest that some of these molecules are useful as prognostic markers in melanoma patients. In cutaneous melanocytic lesions, the distribution of E-cadherin, a member of a family of cell adhesion molecules that mediate cell-cell interactions by means of Ca 2+ dependent, homophilic interactions, appears to be complex. Although a decrease of E-cadherin would be expected with invasive tumour growth in advanced primary melanoma and eventually in metastasis, surprisingly an increase is found, whereas -and -catenin, (cytoplasmic) molecules functionally associated with E-cadherin, are detected in all benign and malignant lesions. A possible interpretation includes a difference in the morphogenesis and function of melanocytic cells, compared with epithelial cells. Further research is needed to clarify the role of E-cadherin/catenin during melanoma progression. 1998 John Wiley & Sons, Ltd.
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Melanoma cells in culture express a variety of growth factors and cytokines and some of their autocrine and paracrine roles have been investigated. However, less information is available on the potential dynamic changes in expression of these molecules on cells during melanoma development and progre