
[Cancer Research 49, 6258-6264, November 15, 1989]
© 1989 American Association for Cancer Research
Sialyltransferase Levels and Ganglioside Expression in Melanoma and Other Cultured Human Cancer Cells1
Immac J. Thampoe,
Koichi Furukawa,
Eugenia Vellvé and
Kenneth O. Lloyd
Memorial Sloan-Kettering Cancer Center, New York, NY 10021
Human melanoma cells express high levels of GM3 and GD3 gangliosides whereas normal melanocytes have only low levels of GD3 but maintain their expression of GM3. In order to understand the basis for this difference, the levels of the sialyltransferase that converts GM3 to GD3 (CMP-N-acetylneuraminic acid:GM3 sialyltransferase or GD3 synthase, EC 2.4.99.8) were analyzed in melanoma and other cell lines. Enzyme levels were determined in vitro using membrane preparations and measuring the addition of [14C]-N-acetylneuraminic acid from CMP-[14C]-N-acetylneuraminic acid to GM3 in the presence of Triton CF-54. Sialyltransferase levels in 44 human cancer cell lines (including melanoma, neuroblastoma, astrocytoma, various carcinomas, and leukemias) and cultures of normal melanocytes and kidney epithelial cells were compared, and the products were identified by thin layer chromatography and fluorography. Melanoma cell lines exhibited the highest levels of incorporation and GD3 was found to be the major product. GM3 was also formed, apparently from endogenous lactosylceramide. Very low levels of GD3 synthase were found in normal melanocytes. Neuroblastoma and some astrocytoma cell lines also had significant levels of GD3 synthase. Some other cell lines incorporated high levels of radioactivity but the products did not correspond to GD3 and the major product was usually GM3. In general the levels of GD3 synthase correlated with the expression of GD3 in the various cell types. These results point to higher levels of GD3 synthase being directly responsible for the enhanced expression of GD3 in melanoma.
1 This work was supported in part by National Cancer Institute Grants CA-08478 and CA-21445.
Received 2/ 3/89.
Revised 7/17/89.
Accepted 8/22/89.
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Copyright © 1989 by the American Association for Cancer Research.