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Discovery and biological characterization of potent myeloid cell leukemia-1 inhibitors.

Authors :
Lee, Taekyu
Bian, Zhiguo
Zhao, Bin
Hogdal, Leah J.
Sensintaffar, John L.
Goodwin, Craig M.
Belmar, Johannes
Shaw, Subrata
Tarr, James C.
Veerasamy, Nagarathanam
Matulis, Shannon M.
Koss, Brian
Fischer, Melissa A.
Arnold, Allison L.
Camper, DeMarco V.
Browning, Carrie F.
Rossanese, Olivia W.
Budhraja, Amit
Opferman, Joseph
Boise, Lawrence H.
Source :
FEBS Letters. Jan2017, Vol. 591 Issue 1, p240-251. 12p.
Publication Year :
2017

Abstract

Myeloid cell leukemia 1 ( Mcl-1) is an antiapoptotic 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. PDB ID codes Comp. 2: ; Comp. 5: . [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00145793
Volume :
591
Issue :
1
Database :
Academic Search Index
Journal :
FEBS Letters
Publication Type :
Academic Journal
Accession number :
120688924
Full Text :
https://doi.org/10.1002/1873-3468.12497