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N-substituted benzamides inhibit NFκB activation and induce apoptosis by separate mechanisms
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  • Published: 29 October 1999

N-substituted benzamides inhibit NFκB activation and induce apoptosis by separate mechanisms

  • D Liberg1,
  • B Lazarevic1,
  • R W Pero2 &
  • …
  • T Leanderson1 

British Journal of Cancer volume 81, pages 981–988 (1999)Cite this article

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Summary

Benzamides have been in clinical use for many years in treatment against various disorders. A recent application is that as a sensitizer for radio- or chemotherapies. We have here analysed the mechanism of action of N-substituted benzamides using an in vitro system. We found that while procainamide was biologically inert in our system, the addition of a chloride in the 3′ position of the benzamide ring created a compound (declopramide) that induced rapid apoptosis. Furthermore, declopramide also inhibited NFκB activation by inhibition of IκBβ breakdown. An acetylated variant of declopramide, N-acetyl declopramide, showed no effect with regard to rapid apoptosis induction but was a potent inhibitor of NFκB activation. In fact, the addition of an acetyl group to procainamide in the 4′ position was sufficient to convert this biologically inactive substance to a potent inhibitor of NFκB activation. These findings suggest two potential mechanisms, induction of early apoptosis and inhibition of NFκB mediated salvage from apoptosis, for the biological effect of N-substituted benzamides as radio- and chemo-sensitizers. In addition it suggests that N-substituted benzamides are potential candidates for the development of anti-inflammatory compounds using NFκB as a drug target.

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  • 16 November 2011

    This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication

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Authors and Affiliations

  1. Immunology, Lund University, Sölvegatan 21, Lund, S-S 62, Sweden

    D Liberg, B Lazarevic & T Leanderson

  2. Department of Cell and Molecular Biology, Molecular Ecogenetic Groups, Lund University, Sölvegatan 21, Lund, S-S 62, Sweden

    R W Pero

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  2. B Lazarevic
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From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/

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Liberg, D., Lazarevic, B., Pero, R. et al. N-substituted benzamides inhibit NFκB activation and induce apoptosis by separate mechanisms. Br J Cancer 81, 981–988 (1999). https://doi.org/10.1038/sj.bjc.6690796

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  • Received: 08 March 1999

  • Revised: 25 May 1999

  • Accepted: 26 May 1999

  • Published: 29 October 1999

  • Issue date: 01 November 1999

  • DOI: https://doi.org/10.1038/sj.bjc.6690796

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Keywords

  • benzamides
  • apoptosis
  • NFκB

This article is cited by

  • Mechanism of action for N-substituted benzamide-induced apoptosis

    • A R Olsson
    • H Lindgren
    • T Leanderson

    British Journal of Cancer (2002)

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