HYZD'ALOVA, M., Jiřina HOFMANOVÁ, Jiří PACHERNÍK, Alena HYRŠLOVÁ VACULOVÁ and Alois KOZUBÍK. The interaction of butyrate with TNF-alpha during differentiation and apoptosis of colon epithelial cells: Role of NF-kappa B activation. Cytokine. Academic Press, 2008, vol. 44, No 1, p. 33-43. ISSN 1043-4666. Available from: https://dx.doi.org/10.1016/j.cyto.2008.06.003.
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Basic information
Original name The interaction of butyrate with TNF-alpha during differentiation and apoptosis of colon epithelial cells: Role of NF-kappa B activation
Authors HYZD'ALOVA, M., Jiřina HOFMANOVÁ (203 Czech Republic), Jiří PACHERNÍK (203 Czech Republic, belonging to the institution), Alena HYRŠLOVÁ VACULOVÁ (203 Czech Republic) and Alois KOZUBÍK (203 Czech Republic, guarantor).
Edition Cytokine, Academic Press, 2008, 1043-4666.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.214
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1016/j.cyto.2008.06.003
UT WoS 000260700600007
Keywords in English Butyrate; TNF-alpha; Differentiation; Apoptosis; NF-kappa B
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 16/6/2020 11:07.
Abstract
We demonstrated that TNF-alpha suppressed differentiation and potentiated cell death induced by butyrate (NaBt) in both adenocarcinoma HT-29 and fetal FHC human colon cells in vitro. Since TNF-alpha is a typical activator of NF-kappa B pathway, we studied the role of NF-kappa B activation in cell differentiation and death during the TNF-alpha and NaBt co-treatment. TNF-alpha induced rapid NF-kappa B activation in both HT-29 and FHC cell lines and this effect was differently modulated by NaBt in these two cell lines. In HT-29 cells, NaBt potentiated NF-kappa B activity induced by TNF-alpha after 4 h treatment. However, this initial potentiation of NF-kappa B activity was not observed in FHC cells. During additional time of TNF-alpha and NaBt co-treatment, NaBt decreased the TNF-alpha-mediated NF-kappa B activity in both cell types. We also detected a different response of HT-29 and FHC cells after the pre-treatment with the NF-kappa B inhibitor parthenolide. Our results indicated that NaBt-mediated differentiation and apoptosis of colon epithelial cells can be modulated by TNF-alpha. Furthermore, we found significant differences in the mechanism of the NaBt and TNF-alpha co-treatment effects between cells of non-cancer and cancer origin, suggesting that the NF-kappa B pathway may be more effectively involved in these processes in cancer cells.
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