Protein synthesis is not required for the inhibitory effect of selenite on cell colony formation and RNA synthesis
- PMID: 7514023
- DOI: 10.1007/BF02950791
Protein synthesis is not required for the inhibitory effect of selenite on cell colony formation and RNA synthesis
Abstract
Selenite has been shown to undergo intracellular metabolism that results in its conversion to other low molecular weight Se-containing species and also to its incorporation into a selenocysteine residue in selenoprotein. In order to investigate whether the incorporation into protein is required for the cytotoxic effects of selenite, we have examined whether inhibition of protein synthesis prevents the inhibitory effect of selenite on the ability of cells to form colonies or to synthesize RNA. We have found that treatment of HeLa cells with cycloheximide inhibited protein synthesis by > 90% but had no effect on the inhibitory effect of selenite on cell colony formation or RNA synthesis. Since protein synthesis is not necessary for these cytotoxic effects of selenite they are unlikely to result from an increase in the synthesis of selenoproteins.
Similar articles
-
Inhibition of colony formation of Hela cells by naturally occurring and synthetic agents.Biofactors. 1995-1996;5(3):133-8. Biofactors. 1995. PMID: 8922269
-
Time-course of inhibition of cellular nucleic acid synthesis by selenite.J Inorg Biochem. 1994 Aug 1;55(2):113-21. doi: 10.1016/0162-0134(94)85033-x. J Inorg Biochem. 1994. PMID: 7519656
-
Effect of cell density on the inhibition of tumor cell attachment and nucleic acid synthesis by selenite.Biol Trace Elem Res. 1993 Nov-Dec;39(2-3):139-47. doi: 10.1007/BF02783184. Biol Trace Elem Res. 1993. PMID: 7509171
-
RNA and protein requirements for eukaryotic selenoprotein synthesis.Biomed Environ Sci. 1997 Sep;10(2-3):182-9. Biomed Environ Sci. 1997. PMID: 9315309 Review.
-
Sodium Selenite as an Anticancer Agent.Anticancer Agents Med Chem. 2017;17(5):658-661. doi: 10.2174/1871520616666160607011024. Anticancer Agents Med Chem. 2017. PMID: 27281365 Review.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources