Antiproliferative effects of selenium compounds in colon cancer cells: comparison of different cytotoxicity assays
Language English Country Great Britain, England Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
19607906
DOI
10.1016/j.tiv.2009.07.013
PII: S0887-2333(09)00188-X
Knihovny.cz E-resources
- MeSH
- Anticarcinogenic Agents therapeutic use toxicity MeSH
- Cysteine analogs & derivatives therapeutic use toxicity MeSH
- Cytotoxins therapeutic use toxicity MeSH
- Humans MeSH
- Methionine analogs & derivatives therapeutic use toxicity MeSH
- Cell Line, Tumor MeSH
- Colonic Neoplasms drug therapy metabolism prevention & control MeSH
- Organoselenium Compounds therapeutic use toxicity MeSH
- Cell Proliferation drug effects MeSH
- Sodium Selenite therapeutic use toxicity MeSH
- Selenocysteine analogs & derivatives MeSH
- Toxicity Tests methods MeSH
- Cell Survival drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Anticarcinogenic Agents MeSH
- Cysteine MeSH
- Cytotoxins MeSH
- Methionine MeSH
- methionine selenoxide MeSH Browser
- Organoselenium Compounds MeSH
- Sodium Selenite MeSH
- Selenocysteine MeSH
- selenomethylselenocysteine MeSH Browser
A number of cytotoxicity assays are currently available, each of them using specific approach to detect different aspects of cell viability, such as cell integrity, proliferation and metabolic functions. In this study we compared the potential of five commonly employed cytotoxicity assays (WST-1, XTT, MTT, Brilliant blue and Neutral red assay) to detect antiproliferative effects of three selenium compounds, sodium selenite, seleno-L-methionine (SeMet) and Se-(Methyl)selenocysteine (SeMCys) on three colorectal cancer cell lines in vitro. Cells were exposed to the selected selenium compounds in the concentration range of 0-256 microM during 48 h. WST-1 and XTT failed to detect cytotoxic effect, with the exception of the highest concentration of selenium compounds tested. Conversely, the metabolic activity of selenium treated cells measured by WST-1 and XTT significantly increased in comparison to untreated controls. MTT, Neutral red and Brilliant blue assays were more sensitive and yielded mutually comparable results, with significant decrease of measured parameters in a concentration-dependent manner. To a smaller extent, the results were affected by the different chemical nature of the selenium compounds tested as well as by the biological properties of individual cell lines.
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