Title of article :
The Natural Anticancer Compounds Rocaglamides Inhibit the Raf-MEK-ERK Pathway by Targeting Prohibitin 1 and 2 Original Research Article
Author/Authors :
Gernot Polier، نويسنده , , Jennifer Neumann، نويسنده , , Frédéric Thuaud، نويسنده , , Nigel Ribeiro، نويسنده , , Christoph Gelhaus، نويسنده , , Jan Hendrik Schmidt، نويسنده , , Marco Giaisi، نويسنده , , Rebecca K?hler، نويسنده , , Wolfgang W. Müller، نويسنده , , Peter Proksch، نويسنده , , Matthias Leippe، نويسنده , , Ottmar Janssen، نويسنده , , Laurent Désaubry، نويسنده , , Peter H. Krammer، نويسنده , , Min Li-Weber، نويسنده ,
Issue Information :
ماهنامه با شماره پیاپی سال 2012
Pages :
12
From page :
1093
To page :
1104
Abstract :
Rocaglamides are potent natural anticancer products that inhibit proliferation of various cancer cells at nanomolar concentrations. We have recently shown that these compounds prevent tumor growth and sensitize resistant cancer cells to apoptosis by blocking the MEK-ERK-eIF4 pathway. However, their direct molecular target(s) remain(s) unknown. In this study, using an affinity chromatography approach we discovered that prohibitin (PHB) 1 and 2 are the direct targets of rocaglamides. Binding of rocaglamides to PHB prevents interaction between PHB and CRaf and, thereby, inhibits CRaf activation and subsequently CRaf-MEK-ERK signaling. Moreover, knockdown of PHB mimicked the effects of rocaglamides on the CRaf-MEK-ERK pathway and cell cycle progression. Thus, our finding suggests that rocaglamides are a new type of anticancer agent and that they may serve as a small-molecular tool for studying PHB-mediated cellular processes.
Journal title :
Chemistry and Biology
Serial Year :
2012
Journal title :
Chemistry and Biology
Record number :
1160306
Link To Document :
بازگشت