c-Jun N-terminal kinase (JNK) signaling: Recent advances and challenges

被引:249
作者
Bogoyevitch, Marie A. [1 ]
Ngoei, Kevin R. W. [1 ]
Zhao, Teresa T. [1 ]
Yeap, Yvonne Y. C. [1 ]
Ng, Dominic C. H. [1 ]
机构
[1] Univ Melbourne, Dept Biochem & Mol Biol, Mol Sci & Biotechnol Inst Bio21, Parkville, Vic 3010, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2010年 / 1804卷 / 03期
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
c-Jun N-terminal kinase (JNK); ATP-competitive inhibitor; ATP non-competitive inhibitor; JNK structure; JNK substrate; Autophagy; microRNA; JNK knockout mouse; JIP1 SCAFFOLD PROTEIN; SMALL-MOLECULE INHIBITORS; NECROSIS-FACTOR-ALPHA; PEPTIDE INHIBITOR; CELL-DEATH; NH2-TERMINAL KINASE; INSULIN-RESISTANCE; CEREBRAL-ISCHEMIA; MAP KINASE; CORTICAL-NEURONS;
D O I
10.1016/j.bbapap.2009.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
c-Jun N-terminal kinases (JNKs), first characterized as stress-activated members of the mitogen-activated protein kinase (MAPK) family, have become a focus of inhibitor screening strategies following studies that have shown their critical roles in the development of a number of diseases, such as diabetes, neurodegeneration and liver disease. We discuss recent advances in the discovery and development of ATP-competitive and ATP-noncompetitive JNK inhibitors. Because understanding the modes of actions of these inhibitors and improving their properties will rely on a better understanding of JNK structure, JNK catalytic mechanisms and substrates, recent advances in these areas of JNK biochemistry are also considered. In addition, the use of JNK gene knockout animals is continuing to reveal in vivo functions for these kinases, with tissue-specific roles now being dissected with tissue-specific knockouts. These latest advances highlight the many challenges now faced, particularly in the directed targeting of the JNK isoforms in specific tissues. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:463 / 475
页数:13
相关论文
共 162 条
[1]   c-Jun N-terminal kinases inhibitor suppresses the TNF-α induced MCP-1 expression in human umbilical vein endothelial cells [J].
Ahmed, Rania Abdel Muneem ;
Murao, Koji ;
Imachi, Hitomi ;
Yoshida, Kazuya ;
Dobashi, Hiroaki ;
Hosomi, Naohisa ;
Ishida, Toshihiko .
ENDOCRINE, 2009, 35 (02) :184-188
[2]   Kinase-targeted libraries: The design and synthesis of novel, potent, and selective kinase inhibitors [J].
Akritopoulou-Zanze, Irini ;
Hajduk, Philip J. .
DRUG DISCOVERY TODAY, 2009, 14 (5-6) :291-297
[3]   Synthesis and SAR of aminopyrimidines as novel c-Jun N-terminal kinase (JNK) inhibitors [J].
Alam, Mahbub ;
Beevers, Rebekah E. ;
Ceska, Tom ;
Davenport, Richard J. ;
Dickson, Karen M. ;
Fortunato, Mara ;
Gowers, Lewis ;
Haughan, Alan F. ;
James, Lynwen A. ;
Jones, Mark W. ;
Kinsella, Natasha ;
Lowe, Christopher ;
Meissner, Johannes W. G. ;
Nicolas, Anne-Lise ;
Perry, Benjamin G. ;
Phillips, David J. ;
Pitt, William R. ;
Platt, Adam ;
Ratcliffe, Andrew J. ;
Sharpe, Andrew ;
Tait, Laura J. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (12) :3463-3467
[4]   N-(3-cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3 [J].
Angell, Richard M. ;
Atkinson, Francis L. ;
Brown, Murray J. ;
Chuang, Tsu Tshen ;
Christopher, John A. ;
Cichy-Knight, Maria ;
Dunn, Allison K. ;
Hightower, Kendra E. ;
Malkakorpi, Susanna ;
Musgrave, James R. ;
Neu, Margarete ;
Rowland, Paul ;
Shea, Robyn L. ;
Smith, Jeffery L. ;
Somers, Donald O. ;
Thomas, Sonia A. ;
Thompson, Gladstone ;
Wang, Ruolan .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (05) :1296-1301
[5]   Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (1) [J].
Asano, Yasutomi ;
Kitamura, Shuji ;
Ohra, Taiichi ;
Aso, Kazuyoshi ;
Igata, Hideki ;
Tamura, Tomoko ;
Kawamoto, Tomohiro ;
Tanaka, Toshimasa ;
Sogabe, Satoshi ;
Matsumoto, Shin-ichi ;
Yamaguchi, Masashi ;
Kimura, Hiroyuki ;
Itoh, Fumio .
BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (08) :4715-4732
[6]  
Asano Y, 2008, BIOORGAN MED CHEM, V16, P4699, DOI 10.1016/j.bmc.2008.02.028
[7]   Phosphorylation of protein phosphatase 2Cζ by c-Jun NH2-terminal kinase at Ser92 attenuates its phosphatase activity [J].
Awano, Kenjiro ;
Amano, Kazutaka ;
Nagaura, Yuko ;
Kanno, Shin-ichiro ;
Echigo, Seishi ;
Tamura, Shinri ;
Kobayashi, Takayasu .
BIOCHEMISTRY, 2008, 47 (27) :7248-7255
[8]   AM-111 reduces hearing loss in a guinea pig model of acute labyrinthitis [J].
Barkdull, Gregory C. ;
Hondarrague, Yannick ;
Meyer, Thomas ;
Harris, Jeffrey P. ;
Keithley, Elizabeth M. .
LARYNGOSCOPE, 2007, 117 (12) :2174-2182
[9]   The critical features and the mechanism of inhibition of a kinase interaction motif-based peptide inhibitor of JNK [J].
Barr, RK ;
Boehm, I ;
Attwood, PV ;
Watt, PM ;
Bogoyevitch, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (35) :36327-36338
[10]   Identification of the critical features of a small peptide inhibitor of JNK activity [J].
Barr, RK ;
Kendrick, TS ;
Bogoyevitch, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :10987-10997