Sesquiterpene lactones have attracted much attention because they display a wide range of biological activities, including antitumor properties. Here, we show the effects of the naturally occurring sesquiterpene lactone asteriscunolide A (AS) on viability of human melanoma, leukemia and cells that o
Altered methionine metabolism occurs in all members of a set of diverse human tumor cell lines
✍ Scribed by Peter H. Stern; C. Douglas Wallace; Robert M. Hoffman
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 574 KB
- Volume
- 119
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
✦ Synopsis
Methionine dependence is a metabolic defect found t h u s far only in transformed and malignant cells. The defect is manifested as the inability of cells to grow in media in which methionine (Met) is replaced by its immediate precursor homocysteiiie (Hcy). We have termed this Met-Hcy+ media. We demonstrate here that methionine-dependent cells derived from human tumors, compared to normal methionine-independent cells, have low levels of free Met, low levels of S-adenosylmethionine (AdoMet) and elevated levels of S-adenosylhomocysteine (AdoHcy) when incubated in Met-Hcy+ medium. Methionine-independent human tumor cells also have very low levels of free Met compared to normal cells but generally have levels of AdoMet and AdoHcy comparable to normal cells in Met-Hcy* medium. All tumor cell types incorporate amounts of Met into protein similar to normal methionineindependent h u m a n fibroblasts when incubated in Met-Hcy+ medium, thereby indicating apparently normal levels of Met synthesis in the tumor cells. The methionine-independent tumor cell lines in Met-Hcy+ medium seem able to regulate their AdoMetiAdoHcy ratios normally despite this defect in having very low levels of free Met. Thus, in a diverse set of human tumor cell lines, all are defective in at least one aspect of Met metabolism, giving rise to the possibility of a general metabolic defect in cancer.
Methionine dependence is a metabolic defect seen in a wide variety of transformed and malignant human and animal cells (Hoffman, 1982;Mecham et al., 1983). This defect is defined as the inability or reduced ability compared to normal cells to grow in culture medium where methionine (Met) is replaced by its immediate precursor homocysteine (Hcy). This medium has been termed Met-Hcy+. The fact that normal cells grow under the
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