desmosterol has been researched along with Multiple-Myeloma* in 2 studies
2 other study(ies) available for desmosterol and Multiple-Myeloma
Article | Year |
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Effects of proximate cholesterol precursors and steroid hormones on mouse myeloma growth in serum-free medium.
The proximate cholesterol precursors lathosterol, 7-dehydrocholesterol and desmosterol supported the growth of NS-1 and X63 mouse myeloma cells. These cells and X63.653 cells are cholesterol auxotrophs, yet each was able to convert [3H]lathosterol to [3H]cholesterol. These results are consistent with the conclusion that cholesterol auxotrophy in these myeloma cells is due to a deficiency in 3-ketosteroid reductase activity. The steroid hormones testosterone, progesterone and hydrocortisone could not replace cholesterol as a medium supplement. These results provide a greater understanding of the cholesterol auxotrophy characteristic of cell lines clonally-derived from the MOPC 21 myeloma tumor, and they provide a rational basis for the use of sterols in defined culture medium for mouse myeloma cells. Topics: 3-Hydroxysteroid Dehydrogenases; Animals; Cell Division; Cholestadienols; Cholesterol; Culture Media; Dehydrocholesterols; Desmosterol; Hormones; Hydrocortisone; Isomerism; Mice; Multiple Myeloma; Progesterone; Testosterone; Tumor Cells, Cultured | 1988 |
Biochemical characterization of the cholesterol-dependent growth of the NS-1 mouse myeloma cell line.
The biochemical basis for the cholesterol-dependent growth phenotype of the NS-1 myeloma cell line has been investigated. In one series of experiments, the growth response of NS-1 cells to several of the intermediates of cholesterol biosynthesis was studied in serum-free medium. The cholesterol precursors, squalene and lanosterol, were totally ineffective in promoting NS-1 cell growth. In contrast, cholesterol precursors downstream from lanosterol, i.e., desmosterol and 7-dehydrocholesterol, completely replaced cholesterol in supporting NS-1 cell growth. In a second series of experiments, NS-1 cells and NS-1-503 cells (a cholesterol growth-independent variant of NS-1 cells) were labelled with [2-14C]acetate and the distributions of radioactivity between cholesterol and its precursors were determined by thin-layer chromatography using two different solvent systems. The major labelled sterol product (greater than 80%) in NS-1 cells after a 24-h exposure to [2-14C]acetate was lanosterol. In contrast, the major labelled sterol product (greater than 95%) in NS-1-503 cells after a 24-h exposure to [2-14C]acetate was cholesterol. Taken together, these results indicate that NS-1 cells are defective in cholesterol biosynthesis and identify the site of lesion as the demethylation of lanosterol to C-29 sterol intermediates. Topics: Acetates; Animals; Cell Division; Cell Line; Cholesterol; Culture Media; Dehydrocholesterols; Desmosterol; Lanosterol; Mice; Multiple Myeloma; Phenotype; Squalene; Sterols | 1986 |