Activation of autophagy and PPARγ protect colon cancer cells against apoptosis induced by interactive effects of butyrate and DHA in a cell type-dependent manner: The role of cell differentiation
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
27840291
DOI
10.1016/j.jnutbio.2016.09.006
PII: S0955-2863(16)30518-6
Knihovny.cz E-zdroje
- Klíčová slova
- Autophagy, Butyrate, Colon cancer, Differentiation, Docosahexaenoic acid, PPARγ,
- MeSH
- antitumorózní látky farmakologie MeSH
- apoptóza účinky léků MeSH
- autofagie účinky léků MeSH
- buněčná diferenciace účinky léků MeSH
- buňky HT-29 MeSH
- butyráty farmakologie MeSH
- HCT116 buňky MeSH
- kaspasa 3 genetika metabolismus MeSH
- kyselina máselná farmakologie MeSH
- kyseliny dokosahexaenové farmakologie MeSH
- lidé MeSH
- mitochondrie účinky léků metabolismus MeSH
- nádory tračníku patologie MeSH
- PPAR gama genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antitumorózní látky MeSH
- butyráty MeSH
- CASP3 protein, human MeSH Prohlížeč
- kaspasa 3 MeSH
- kyselina máselná MeSH
- kyseliny dokosahexaenové MeSH
- PPAR gama MeSH
The short-chain and n-3 polyunsaturated fatty acids exhibit anticancer properties, and they may mutually interact within the colon. However, the molecular mechanisms of their action in colon cancer cells are still not fully understood. Our study focused on the mechanisms responsible for the diverse effects of sodium butyrate (NaBt), in particular when interacting with docosahexaenoic acid (DHA), in distinct colon cancer cell types, in which NaBt either induces cell differentiation or activates programmed cell death involving mitochondrial pathway. NaBt activated autophagy both in HT-29 cells, which are sensitive to induction of differentiation, and in nondifferentiating HCT-116 cells. However, autophagy supported cell survival only in HT-29 cells. Combination of NaBt with DHA-promoted cell death, especially in HCT-116 cells and after longer time intervals. The inhibition of autophagy both attenuated differentiation and enhanced apoptosis in HT-29 cells treated with NaBt and DHA, but it had no effect in HCT-116 cells. NaBt, especially in combination with DHA, activated PPARγ in both cell types. PPARγ silencing decreased differentiation and increased apoptosis only in HT-29 cells, therefore we verified the role of caspases in apoptosis, differentiation and also PPARγ activity using a pan-caspase inhibitor. In summary, our data suggest that diverse responses of colon cancer cells to fatty acids may rely on their sensitivity to differentiation, which may in turn depend on distinct engagement of autophagy, caspases and PPARγ. These results contribute to understanding of mechanisms underlying differential effects of NaBt, when interacting with other dietary fatty acids, in colon cancer cells.
Department of Cytokinetics Institute of Biophysics The Czech Academy of Sciences Brno Czech Republic
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