Deciphering the true antiproliferative target of an MK2 activation inhibitor in glioblastoma

被引:3
作者
Brennan, P. E. [1 ]
机构
[1] Univ Oxford, Struct Genom Consortium, Target Discovery Inst, Nuffield Dept Med, Oxford OX3 7FZ, England
关键词
PROTEIN-KINASE; 2; CHEMICAL PROBES; DISCOVERY;
D O I
10.1038/cddis.2015.384
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
引用
收藏
页码:e2069 / e2069
页数:3
相关论文
共 14 条
[1]   Pyrrolopyridine inhibitors of mitogen-activated protein kinase-activated protein kinase 2 (MK-2) [J].
Anderson, David R. ;
Meyers, Marvin J. ;
Vernier, William F. ;
Mahoney, Matthew W. ;
Kurumbail, Ravi G. ;
Caspers, Nicole ;
Poda, Gennadiy I. ;
Schindler, John F. ;
Reitz, David B. ;
Mourey, Robert J. .
JOURNAL OF MEDICINAL CHEMISTRY, 2007, 50 (11) :2647-2654
[2]   The promise and peril of chemical probes [J].
Arrowsmith, Cheryl H. ;
Audia, James E. ;
Austin, Christopher ;
Baell, Jonathan ;
Bennett, Jonathan ;
Blagg, Julian ;
Bountra, Chas ;
Brennan, Paul E. ;
Brown, Peter J. ;
Bunnage, Mark E. ;
Buser-Doepner, Carolyn ;
Campbell, Robert M. ;
Carter, Adrian J. ;
Cohen, Philip ;
Copeland, Robert A. ;
Cravatt, Ben ;
Dahlin, Jayme L. ;
Dhanak, Dashyant ;
Edwards, Aled M. ;
Frye, Stephen V. ;
Gray, Nathanael ;
Grimshaw, Charles E. ;
Hepworth, David ;
Howe, Trevor ;
Huber, Kilian V. M. ;
Jin, Jian ;
Knapp, Stefan ;
Kotz, Joanne D. ;
Kruger, Ryan G. ;
Lowe, Derek ;
Mader, Mary M. ;
Marsden, Brian ;
Mueller-Fahrnow, Anke ;
Mueller, Susanne ;
O'Hagan, Ronan C. ;
Overington, John P. ;
Owen, Dafydd R. ;
Rosenberg, Saul H. ;
Roth, Brian ;
Ross, Ruth ;
Schapira, Matthieu ;
Schreiber, Stuart L. ;
Shoichet, Brian ;
Sundstrom, Michael ;
Superti-Furga, Giulio ;
Taunton, Jack ;
Toledo-Sherman, Leticia ;
Walpole, Chris ;
Walters, Michael A. ;
Willson, Timothy M. .
NATURE CHEMICAL BIOLOGY, 2015, 11 (08) :536-541
[3]   Target validation using chemical probes [J].
Bunnage, Mark E. ;
Chekler, Eugene L. Piatnitski ;
Jones, Lyn H. .
NATURE CHEMICAL BIOLOGY, 2013, 9 (04) :195-199
[4]   Dual kinase-bromodomain inhibitors for rationally designed polypharmacology [J].
Ciceri, Pietro ;
Mueller, Susanne ;
O'Mahony, Alison ;
Fedorov, Oleg ;
Filippakopoulos, Panagis ;
Hunt, Jeremy P. ;
Lasater, Elisabeth A. ;
Pallares, Gabriel ;
Picaud, Sarah ;
Wells, Christopher ;
Martin, Sarah ;
Wodicka, Lisa M. ;
Shah, Neil P. ;
Treiber, Daniel K. ;
Knapp, Stefan .
NATURE CHEMICAL BIOLOGY, 2014, 10 (04) :305-+
[5]   Discovery and characterization of a substrate selective p38α inhibitor [J].
Davidson, W ;
Frego, L ;
Peet, GW ;
Kroe, RR ;
Labadia, ME ;
Lukas, SM ;
Snow, RJ ;
Jakes, S ;
Grygon, CA ;
Pargellis, C ;
Werneburg, BG .
BIOCHEMISTRY, 2004, 43 (37) :11658-11671
[6]   Profile of the GSK Published Protein Kinase Inhibitor Set Across ATP-Dependent and-Independent Luciferases: Implications for Reporter-Gene Assays [J].
Dranchak, Patricia ;
MacArthur, Ryan ;
Guha, Rajarshi ;
Zuercher, William J. ;
Drewry, David H. ;
Auld, Douglas S. ;
Inglese, James .
PLOS ONE, 2013, 8 (03)
[7]   Cytotoxic activity of the MK2 inhibitor CMPD1 in glioblastoma cells is independent of MK2 [J].
Gurgis, F. M. S. ;
Akerfeld, M. C. ;
Heng, B. ;
Wong, C. ;
Adams, S. ;
Guillemin, G. J. ;
Johns, T. G. ;
Chircop, M. ;
Munoz, L. .
CELL DEATH DISCOVERY, 2015, 1
[8]   Mitogen-Activated Protein Kinase-Activated Protein Kinase 2 in Neuroinflammation, Heat Shock Protein 27 Phosphorylation, and Cell Cycle: Role and Targeting [J].
Gurgis, Fadi Maged Shokry ;
Ziaziaris, William ;
Munoz, Lenka .
MOLECULAR PHARMACOLOGY, 2014, 85 (02) :345-356
[9]   Cytotoxic Activity of Tivantinib (ARQ 197) Is Not Due Solely to c-MET Inhibition [J].
Katayama, Ryohei ;
Aoyama, Aki ;
Yamori, Takao ;
Qi, Jie ;
Oh-hara, Tomoko ;
Song, Youngchul ;
Engelman, Jeffrey A. ;
Fujita, Naoya .
CANCER RESEARCH, 2013, 73 (10) :3087-3096
[10]   Comparing Immobilized Kinase Inhibitors and Covalent ATP Probes for Proteomic Profiling of Kinase Expression and Drug Selectivity [J].
Lemeer, Simone ;
Zoergiebel, Gonna ;
Ruprecht, Benjamin ;
Kohl, Kristian ;
Kuster, Bernhard .
JOURNAL OF PROTEOME RESEARCH, 2013, 12 (04) :1723-1731