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Proteasome Inhibitors as Therapeutic Agents: Current and Future Strategies

[ Vol. 10 , Issue. 6 ]


J. G. Delcros, M. Baudy Floc'h, C. Prigent and Y. Arlot-Bonnemains   Pages 479 - 503 ( 25 )


In cells, protein degradation is a key pathway for the destruction of abnormal or damaged proteins as well as for the elimination of proteins whose presence is no longer required. Among the various cell proteases, the proteasome, a multicatalytic macromolecular complex, is specifically required for the degradation of ubiquitinated proteins. In normal cells, the proteasome ensures the elimination of numerous proteins that play critical roles in cell functions throughout the cell cycle. Defects in the activity of this proteolytic machinery can lead to the disorders of cell function that is believed to be the root cause of certain diseases. Indeed, many proteins involved in the control of cell cycle transitions are readily destroyed by the proteasome once their tasks have been accomplished. Moreover, because proteasome inhibitors can provoke cell death, it has been suggested that proteasomes must be continually degrading certain apoptotic factors. For these reasons, proteasome inhibition has become a new and potentially significant strategy for the drug development in cancer treatment. The proteasome possesses three major peptidase activities that can individually be targeted by drugs. Different classes of proteasome inhibitors are reviewed here. In addition, we present new pseudopeptides with the enriched nitrogen backbones bearing a side chain and a modified C-terminal position that inhibit proteasome activity.


Proteasome Inhibitors,pseudopeptides,apoptotic factors


, , , Groupe Cycle Cellulaire, CNRS UMR 6061 Genetique et Developpement, IFR 97 Genomique Fonctionnelle et Sante, Faculte de Medecine, Universite Rennes 1, 2 av du Pr Leon Bernard, CS 34317, 35043 Rennes Cedex, France

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