Abstract
Malignant melanoma cells can differentiate spontaneously in vivo and in vitro into cells with a finite lifespan. Analysis of differentiating cells from primary melanomas in culture revealed a flat, fibroblast‐like morphology and expression of the fibroblast‐associated marker leucine aminopeptidase (LAP). Differentiation was also observed in a minor sub‐population of permanent cell lines derived from metastatic lesions. An experimental model of melanoma cell differentiation was then developed, using the pyrimidine analog bromodeoxyuridine (BUdR). BUdR‐treated cells had a flat morphology, were contact‐inhibited, had up to 20‐fold increased surface area, expressed LAP, no longer proliferated anchorage‐independently in soft agar, and 3 out of 4 cell lines were non‐tumorigenic in athymic nude mice. Our results show that models of differentiation of melanoma cells can be established that help to define pathways of differentiation.
| Original language | English |
|---|---|
| Pages (from-to) | 159-165 |
| Number of pages | 7 |
| Journal | International Journal of Cancer |
| Volume | 54 |
| Issue number | 1 |
| DOIs | |
| State | Published - 22 04 1993 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
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