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Discovery and biological characterization of potent myeloid cell leukemia‐1 inhibitors

Authors :
Edward T. Olejniczak
Melissa A. Fischer
DeMarco V. Camper
Taekyu Lee
Lawrence H. Boise
Michael R. Savona
Leah Hogdal
Carrie F. Browning
Brian Koss
Bin Zhao
Anthony Letai
Johannes Belmar
James C. Tarr
Olivia W. Rossanese
Nagarathanam Veerasamy
Zhiguo Bian
Amit Budhraja
Shannon M. Matulis
Stephen W. Fesik
Subrata Shaw
John Sensintaffar
Joseph T. Opferman
Craig M. Goodwin
Allison L. Arnold
Source :
FEBS Letters. 591:240-251
Publication Year :
2016
Publisher :
Wiley, 2016.

Abstract

Mcl-1 is an anti-apoptotic member of the Bcl-2 family of proteins that when overexpressed is associated with high tumor grade, poor survival, and resistance to chemotherapy. Mcl-1 is amplified in many human cancers, and knockdown of Mcl-1 using RNAi can lead to apoptosis. Thus, Mcl-1 is a promising cancer target. Here, we describe the discovery of picomolar Mcl-1 inhibitors that cause caspase activation, mitochondrial depolarization, and selective growth inhibition. These compounds represent valuable tools to study the role of Mcl-1 in cancer and serve as useful starting points for the discovery of clinically useful Mcl-1 inhibitors. This article is protected by copyright. All rights reserved.

Details

ISSN :
18733468 and 00145793
Volume :
591
Database :
OpenAIRE
Journal :
FEBS Letters
Accession number :
edsair.doi...........a7b42e25c5eb5c232c4857969b56b317