Metastatic variant sublines of the murine RAW117 large cell lymphoma or lymphosarcoma have been established in vitro by sequential cycles of harvesting of liver tumor nodules after intravenous inoculation of tumor cell suspensions into syngeneic BALB/c mice. After five and ten in vivo selections for
Differential expression of cell adhesion molecules in variants of K1735 melanoma cells differing in metastatic capacity
β Scribed by Dorte Linnemann; Avraham Raz; Elisabeth Bock
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- French
- Weight
- 515 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
β¦ Synopsis
We have investigated the expression of 2 neural-cell adhesion molecules, NCAM and LI, in K1735-CI16 and -MI melanoma cells which differ qualitatively in their metastatic potential, i.e., M l cells are metastatic whereas CI 16 cells are not. We have found that NCAM in C116 cells are expressed as 2 quantitatively major glycosylated polypeptides with Mr of 145,000 and 120,000 and a minor 190,000 Mr polypeptide, whereas M I cells expressed NCAM as 3 glycosylated polypeptides with Mr of 200,000, I40,OOO and 120.000. The amount of NCAM in MI cells constituted only 60% of the amount observed in C116 cells. In C116 cells, the 145,000 and 120,000 Mr NCAM polypeptides were sulphated whereas NCAM did not appear to be sulphated in M I cells. No phosphorylation of NCAM in the 2 cell lines was observed. L I was expressed as a phosphorylated glycoprotein with Mr of 210,000 in M I cells whereas no L I expression was observed in C116 cells. L I was not sulphated in MI cells.
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