Protein Kinases and Parkinson's Disease

被引:25
作者
Mehdi, Syed Jafar [1 ]
Rosas-Hernandez, Hector [2 ]
Cuevas, Elvis [2 ]
Lantz, Susan M. [2 ]
Barger, Steven W. [1 ,3 ]
Sarkar, Sumit [2 ]
Paule, Merle G. [2 ]
Ali, Syed F. [2 ]
Imam, Syed Z. [1 ,2 ]
机构
[1] Univ Arkansas Med Sci, Dept Geriatr, Little Rock, AR 72205 USA
[2] US FDA, Div Neurotoxicol, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA
[3] Cent Arkansas Vet Healthcare Syst, Ctr Geriatr Res Educ & Clin, Little Rock, AR 72205 USA
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2016年 / 17卷 / 09期
关键词
Parkinson's disease; dopamine; tyrosine kinase; serine/threonine kinase; kinase inhibitors; CEREBELLAR GRANULE NEURONS; DOPAMINERGIC CELL-DEATH; G2019S LRRK2 MUTATION; JNK ACTIVATION; MOUSE MODEL; IN-VIVO; C-ABL; SIGNALING PATHWAY; INDUCED APOPTOSIS; TYROSINE KINASES;
D O I
10.3390/ijms17091585
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
Currently, the lack of new drug candidates for the treatment of major neurological disorders such as Parkinson's disease has intensified the search for drugs that can be repurposed or repositioned for such treatment. Typically, the search focuses on drugs that have been approved and are used clinically for other indications. Kinase inhibitors represent a family of popular molecules for the treatment and prevention of various cancers, and have emerged as strong candidates for such repurposing because numerous serine/threonine and tyrosine kinases have been implicated in the pathobiology of Parkinson's disease. This review focuses on various kinase-dependent pathways associated with the expression of Parkinson's disease pathology, and evaluates how inhibitors of these pathways might play a major role as effective therapeutic molecules.
引用
收藏
页数:12
相关论文
共 93 条
[1]   Expanding insights of mitochondrial dysfunction in Parkinson's disease [J].
Abou-Sleiman, PM ;
Muqit, MMK ;
Wood, NW .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (03) :207-219
[2]   Tauroursodeoxycholic Acid Prevents MPTP-Induced Dopaminergic Cell Death in a Mouse Model of Parkinson's Disease [J].
Castro-Caldas, M. ;
Carvalho, A. Neves ;
Rodrigues, E. ;
Henderson, C. J. ;
Wolf, C. R. ;
Rodrigues, C. M. P. ;
Gama, M. J. .
MOLECULAR NEUROBIOLOGY, 2012, 46 (02) :475-486
[3]   Blocking c-Jun N-terminal Kinase (JNK) Translocation to the Mitochondria Prevents 6-Hydroxydopamine-induced Toxicity in Vitro and in Vivo [J].
Chambers, Jeremy W. ;
Howard, Shannon ;
LoGrasso, Philip V. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2013, 288 (02) :1079-1087
[4]   Small Molecule c-jun-N-Terminal Kinase Inhibitors Protect Dopaminergic Neurons in a Model of Parkinson's Disease [J].
Chambers, Jeremy W. ;
Pachori, Alok ;
Howard, Shannon ;
Ganno, Michelle ;
Hansen, Donald, Jr. ;
Kamenecka, Ted ;
Song, Xinyi ;
Duckett, Derek ;
Chen, Weimin ;
Ling, Yuan Yuan ;
Cherry, Lisa ;
Cameron, Michael D. ;
Lin, Li ;
Ruiz, Claudia H. ;
LoGrasso, Philip .
ACS CHEMICAL NEUROSCIENCE, 2011, 2 (04) :198-206
[5]  
Choi WS, 1999, J NEUROSCI RES, V57, P86, DOI 10.1002/(SICI)1097-4547(19990701)57:1<86::AID-JNR9>3.3.CO
[6]  
2-5
[7]   Frequency of LRRK2 mutations in early- and late-onset Parkinson disease [J].
Clark, L. N. ;
Wang, Y. ;
Karlins, E. ;
Saito, L. ;
Mejia-Santana, H. ;
Harris, J. ;
Louis, E. D. ;
Cote, L. J. ;
Andrews, H. ;
Fahn, S. ;
Waters, C. ;
Ford, B. ;
Frucht, S. ;
Ottman, R. ;
Marder, K. .
NEUROLOGY, 2006, 67 (10) :1786-1791
[8]   Parkinson's disease: insights from pathways [J].
Cookson, Mark R. ;
Bandmann, Oliver .
HUMAN MOLECULAR GENETICS, 2010, 19 :R21-R27
[9]   How genetics research in Parkinson's disease is enhancing understanding of the common idiopathic forms of the disease [J].
Cookson, MR ;
Xiromerisiou, G ;
Singleton, A .
CURRENT OPINION IN NEUROLOGY, 2005, 18 (06) :706-711
[10]  
Dächsel JC, 2010, ARCH NEUROL-CHICAGO, V67, P542, DOI 10.1001/archneurol.2010.79