Histone deacetylases: novel targets for prevention of colitis-associated cancer in mice.

Details

Serval ID
serval:BIB_1BFA97FF3AC5
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Histone deacetylases: novel targets for prevention of colitis-associated cancer in mice.
Journal
Gut
Author(s)
Glauben R., Batra A., Stroh T., Erben U., Fedke I., Lehr H.A., Leoni F., Mascagni P., Dinarello C.A., Zeitz M., Siegmund B.
ISSN
1468-3288[electronic]
Publication state
Published
Issued date
2008
Volume
57
Number
5
Pages
613-622
Language
english
Abstract
OBJECTIVE: Inhibition of histone deacetylases, well known for its antiproliferative efficacy in vivo, was recently shown to ameliorate inflammation in experimental colitis. Since inflammatory bowel disease is associated with an increased risk of developing colon cancer, here the combined anti-inflammatory and proapoptotic efficacy of histone deacetylase inhibitors was studied in mouse models. METHODS: The novel histone deacetylase inhibitor ITF2357 was compared with suberoylanilide hydroxamic acid in models of experimental colitis. Effects on tumour growth were studied after treatment of mice with azoxymethane and dextran sulphate sodium, and in interleukin 10 (IL10) knockout mice, respectively. Possible underlying mechanisms involving apoptosis and nuclear factor (NF)-kappaB activation were addressed by flow cytometry and western blot. RESULTS: In dextran sulphate sodium- and trinitrobenzene sulphonic acid-induced colitis, treatment with ITF2357 was superior to suberoylanilide hydroxamic acid as shown by macroscopic and histological amelioration of inflammation, by reduced production of interferon gamma (IFN gamma) and by increased production of IL10. In both models of inflammation-mediated tumourigenesis, inhibition of histone deacetylases resulted in a significant suppression of tumour growth in terms of size and number, along with reduced signs of inflammation. As for potential mechanisms of ITF2357 action, increased acetylation of histone 3, reduced production of IFN gamma and enhanced apoptosis in lamina propria mononuclear cells were found to accompany a histone deacetylase-dependent activation of NF-kappaB. CONCLUSIONS: These results indicate that inhibition of histone deactylases can attenuate inflammation-mediated tumour growth, which is paralled by an inhibition of NF-kappaB. Thus histone deacetylase inhibitors provide a promising strategy that combines anti-inflammatory and proapoptotic modes of action.
Keywords
Animals, Anti-Inflammatory Agents, Anticarcinogenic Agents, Apoptosis, Colitis, Colonic Neoplasms, Cytokines, Dose-Response Relationship, Drug, Female, Histone Deacetylases, Hydroxamic Acids, Mice, Mice, Inbred C57BL, Mice, Knockout, NF-kappa B
Pubmed
Web of science
Create date
06/02/2008 9:58
Last modification date
20/08/2019 12:52
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