TNF-alpha modulates the differentiation induced by butyrate in the HT-29 human colon adenocarcinoma cell line
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
10974633
DOI
10.1016/s0959-8049(00)00178-7
PII: S0959-8049(00)00178-7
Knihovny.cz E-resources
- MeSH
- Alkaline Phosphatase metabolism MeSH
- Apoptosis MeSH
- HT29 Cells drug effects metabolism pathology MeSH
- Butyrates therapeutic use MeSH
- Cadherins metabolism MeSH
- Humans MeSH
- Cell Transformation, Neoplastic MeSH
- Neoplasm Proteins metabolism MeSH
- Tumor Necrosis Factor-alpha therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Alkaline Phosphatase MeSH
- Butyrates MeSH
- Cadherins MeSH
- Neoplasm Proteins MeSH
- Tumor Necrosis Factor-alpha MeSH
The aim of this study was to determine whether and how tumour necrosis factor alpha (TNF-alpha) modulates butyrate effects. After the treatment of human colon adenocarcinoma HT-29 cells with sodium butyrate (NaBt), TNF-alpha or with their combinations we detected cell cycle (flow cytometry), cell proliferation (amidoblack and MTT assays), the amount of dead (floating) and apoptotic cells (flow cytometry and fluorescence microscopy), and the level of differentiation by alkaline phosphatase (ALP) activity (spectrophotometry), relative F-actin content (confocal laser scanning microscopy analysis) and E-cadherin expression (Western blot analysis). Both TNF-alpha and NaBt decreased cell growth in a dose-dependent manner. After combined treatment of the cells with both agents used, either none or additive effects were observed as compared with NaBt treatment alone. The level of dead and apoptotic cells was dose-dependently increased after this combined treatment. In contrast, TNF-alpha suppressed ALP activity and F-actin accumulation induced by NaBt. The results suggest that TNF-alpha does not influence significantly the antiproliferative effects of NaBt but, contrary to its potentiation of apoptosis, it markedly reduces NaBt-induced differentiation of HT-29 colon adenocarcinoma cells.
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