Cargando…
The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia
Nuclear factor-κB (NF-κB) is an important regulator of cell survival and has been shown to be constitutively active in chronic lymphocytic leukemia (CLL) cells. Recently, a novel NF-κB inhibitor, IMD-0354 (N-(3, 5-bis-trifluoromethyl-phenyl)-5-chloro-2-hydroxy-benzamide), was shown to specifically i...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255277/ https://www.ncbi.nlm.nih.gov/pubmed/22829125 http://dx.doi.org/10.1038/bcj.2011.9 |
_version_ | 1782220974059421696 |
---|---|
author | Kanduri, M Tobin, G Åleskog, A Nilsson, K Rosenquist, R |
author_facet | Kanduri, M Tobin, G Åleskog, A Nilsson, K Rosenquist, R |
author_sort | Kanduri, M |
collection | PubMed |
description | Nuclear factor-κB (NF-κB) is an important regulator of cell survival and has been shown to be constitutively active in chronic lymphocytic leukemia (CLL) cells. Recently, a novel NF-κB inhibitor, IMD-0354 (N-(3, 5-bis-trifluoromethyl-phenyl)-5-chloro-2-hydroxy-benzamide), was shown to specifically inhibit the phosphorylation of IκBα by IkB kinases, thus preventing NF-κB release. In this study, we investigated if IMD-0354 can inhibit NF-κB activation and induce apoptosis in CLL cells in vitro. The rate of increase in apoptosis, drug sensitivity and DNA-binding activity of NF-κB were studied using Annexin V stainings, the fluorometric microculture cytotoxicity assay and electrophoretic mobility shift assay, respectively. Finally, the impact of IMD-0354 treatment on the expression of a set of apoptosis-related genes was investigated. The results clearly show that IMD-0354 induced apoptosis (mean 26%, range 8–48%) in CLL cells, independent of immunoglobulin heavy variable (IGHV) gene mutational status, and showed a dose-dependent cytotoxic effect. IMD-0354 treatment also significantly lowered the DNA-binding activity of NF-κB in CLL cells. In addition, we identified differences in expression levels of pro- and antiapoptotic genes following IMD-0354 treatment. In summary, our novel findings show that IMD-0354 can induce apoptosis in CLL cells, and thus merits further investigation as an anticancer agent in vivo. |
format | Online Article Text |
id | pubmed-3255277 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32552772012-01-11 The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia Kanduri, M Tobin, G Åleskog, A Nilsson, K Rosenquist, R Blood Cancer J Original Article Nuclear factor-κB (NF-κB) is an important regulator of cell survival and has been shown to be constitutively active in chronic lymphocytic leukemia (CLL) cells. Recently, a novel NF-κB inhibitor, IMD-0354 (N-(3, 5-bis-trifluoromethyl-phenyl)-5-chloro-2-hydroxy-benzamide), was shown to specifically inhibit the phosphorylation of IκBα by IkB kinases, thus preventing NF-κB release. In this study, we investigated if IMD-0354 can inhibit NF-κB activation and induce apoptosis in CLL cells in vitro. The rate of increase in apoptosis, drug sensitivity and DNA-binding activity of NF-κB were studied using Annexin V stainings, the fluorometric microculture cytotoxicity assay and electrophoretic mobility shift assay, respectively. Finally, the impact of IMD-0354 treatment on the expression of a set of apoptosis-related genes was investigated. The results clearly show that IMD-0354 induced apoptosis (mean 26%, range 8–48%) in CLL cells, independent of immunoglobulin heavy variable (IGHV) gene mutational status, and showed a dose-dependent cytotoxic effect. IMD-0354 treatment also significantly lowered the DNA-binding activity of NF-κB in CLL cells. In addition, we identified differences in expression levels of pro- and antiapoptotic genes following IMD-0354 treatment. In summary, our novel findings show that IMD-0354 can induce apoptosis in CLL cells, and thus merits further investigation as an anticancer agent in vivo. Nature Publishing Group 2011-03 2011-03-25 /pmc/articles/PMC3255277/ /pubmed/22829125 http://dx.doi.org/10.1038/bcj.2011.9 Text en Copyright © 2011 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Original Article Kanduri, M Tobin, G Åleskog, A Nilsson, K Rosenquist, R The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title | The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title_full | The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title_fullStr | The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title_full_unstemmed | The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title_short | The novel NF-κB inhibitor IMD-0354 induces apoptosis in chronic lymphocytic leukemia |
title_sort | novel nf-κb inhibitor imd-0354 induces apoptosis in chronic lymphocytic leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255277/ https://www.ncbi.nlm.nih.gov/pubmed/22829125 http://dx.doi.org/10.1038/bcj.2011.9 |
work_keys_str_mv | AT kandurim thenovelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT tobing thenovelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT aleskoga thenovelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT nilssonk thenovelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT rosenquistr thenovelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT kandurim novelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT tobing novelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT aleskoga novelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT nilssonk novelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia AT rosenquistr novelnfkbinhibitorimd0354inducesapoptosisinchroniclymphocyticleukemia |