Abstract
Shedding by cultured human melanoma cells of a well-characterised cell-surface glycoprotein antigen known as 'melanotransferrin' was studied with two monoclonal antibodies, 140.240 and 96.5. By means of [(35)(S)]-cysteine metabolically-labelled melanoma cells and immunoprecipitation studies, identification was made, by 140.240 in the spent media of two of six melanoma cell lines, of a new molecule of 100-kDa, aside from the 88-kDa molecule. Only the 88-kDa shed molecule was detected in the remaining four melanoma cell lines with both antibodies. None of nine clonal sublines derived from the two melanoma cell lines were found to shed the 100kDa or 88-kDa molecule exclusively.. Both shed antigens were released spontaneously to the medium from the live melanoma cells rather than as a result of cell death and lysis, since there was no obvious cell death or debris in the spent medium nor in the monolayer cells detected at the time of spent medium collection.
| Original language | English |
|---|---|
| Pages (from-to) | 171-176 |
| Number of pages | 6 |
| Journal | Anticancer Research |
| Volume | 16 |
| Issue number | 1 |
| State | Published - 01 1996 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Antigen shedding
- Glycosylation
- Melanoma
- Melanotransferrin
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