Ubiquitination in disease pathogenesis and treatment

被引:1078
作者
Popovic, Doris [1 ,2 ]
Vucic, Domagoj [3 ]
Dikic, Ivan [1 ,2 ,4 ]
机构
[1] Goethe Univ Frankfurt, Sch Med, Univ Hosp, Inst Biochem 2, Frankfurt, Germany
[2] Goethe Univ Frankfurt, Sch Med, Univ Hosp, Buchmann Inst Mol Life Sci, Frankfurt, Germany
[3] Genentech Inc, Dept Early Discovery Biochem, San Francisco, CA 94080 USA
[4] Univ Split, Sch Med, Dept Immunol, Split, Croatia
基金
欧洲研究理事会;
关键词
SMALL-MOLECULE INHIBITOR; ACTIVATING ENZYME E1; KAPPA-B PATHWAY; ALPHA-SYNUCLEIN; PROTEASOME SYSTEM; MULTIPLE-MYELOMA; HUNTINGTONS-DISEASE; FANCONI-ANEMIA; MUSCLE ATROPHY; INCONTINENTIA PIGMENTI;
D O I
10.1038/nm.3739
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
Ubiquitination is crucial for a plethora of physiological processes, including cell survival and differentiation and innate and adaptive immunity. In recent years, considerable progress has been made in the understanding of the molecular action of ubiquitin in signaling pathways and how alterations in the ubiquitin system lead to the development of distinct human diseases. Here we describe the role of ubiquitination in the onset and progression of cancer, metabolic syndromes, neurodegenerative diseases, autoimmunity, inflammatory disorders, infection and muscle dystrophies. Moreover, we indicate how current knowledge could be exploited for the development of new clinical therapies.
引用
收藏
页码:1242 / 1253
页数:12
相关论文
共 168 条
[1]   Muscle Wasting in Aged, Sarcopenic Rats Is Associated with Enhanced Activity of the Ubiquitin Proteasome Pathway [J].
Altun, Mikael ;
Besche, Henrike C. ;
Overkleeft, Herman S. ;
Piccirillo, Rosanna ;
Edelmann, Mariola J. ;
Kessler, Benedikt M. ;
Goldberg, Alfred L. ;
Ulfhake, Brun .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (51) :39597-39608
[2]   Phosphorylation of Ser-129 is the dominant pathological modification of α-synuclein in familial and sporadic Lewy body disease [J].
Anderson, John P. ;
Walker, Donald E. ;
Goldstein, Jason M. ;
de laat, Rian ;
Banducci, Kelly ;
Caccavello, Russell J. ;
Barbour, Robin ;
Huang, Jiping ;
Kling, Kristin ;
Lee, Michael ;
Diep, Linnea ;
Keim, Pamela S. ;
Shen, Xiaofeng ;
Chataway, Tim ;
Schlossmacher, Michael G. ;
Seubert, Peter ;
Schenk, Dale ;
Sinha, Sukanto ;
Gai, Wei Ping ;
Chilcote, Tamie J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (40) :29739-29752
[3]   Frequent engagement of the classical and alternative NF-κB pathways by diverse genetic abnormalities in multiple myeloma [J].
Annunziata, Christina M. ;
Davis, R. Eric ;
Demchenko, Yulia ;
Bellamy, William ;
Gabrea, Ana ;
Zhan, Fenghuang ;
Lenz, Georg ;
Hanamura, Ichiro ;
Wright, George ;
Xiao, Wenming ;
Dave, Sandeep ;
Hurt, Elaine M. ;
Tan, Bruce ;
Zhao, Hong ;
Stephens, Owen ;
Santra, Madhumita ;
Williams, David R. ;
Dang, Lenny ;
Barlogie, Bart ;
Shaughnessy, John D., Jr. ;
Kuehl, W. Michael ;
Staudt, Louis M. .
CANCER CELL, 2007, 12 (02) :115-130
[4]   Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-γ) [J].
Aradhya, S ;
Courtois, G ;
Rajkovic, A ;
Lewis, RA ;
Levy, M ;
Israël, A ;
Nelson, DL .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (03) :765-771
[5]   A recurrent deletion in the ubiquitously expressed NEMO (IKK-γ) gene accounts for the vast majority of incontinentia pigmenti mutations [J].
Aradhya, S ;
Woffendin, H ;
Jakins, T ;
Bardaro, T ;
Esposito, T ;
Smahi, A ;
Shaw, C ;
Levy, M ;
Munnich, A ;
D'Urso, M ;
Lewis, RA ;
Kenwrick, S ;
Nelson, DL .
HUMAN MOLECULAR GENETICS, 2001, 10 (19) :2171-2179
[6]   BAG-2 acts as an inhibitor of the chaperone-associated ubiquitin ligase CHIP [J].
Arndt, V ;
Daniel, C ;
Nastainczyk, W ;
Alberti, S ;
Höhfeld, J .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (12) :5891-5900
[7]   Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance [J].
Arndt, Verena ;
Dick, Nikolaus ;
Tawo, Riga ;
Dreiseidler, Michael ;
Wenzel, Daniela ;
Hesse, Michael ;
Fuerst, Dieter O. ;
Saftig, Paul ;
Saint, Robert ;
Fleischmann, Bernd K. ;
Hoch, Michael ;
Hoehfeld, Joerg .
CURRENT BIOLOGY, 2010, 20 (02) :143-148
[8]   Sequestosome 1/p62 shuttles polyubiquitinated tau for proteasomal degradation [J].
Babu, JR ;
Geetha, T ;
Wooten, MW .
JOURNAL OF NEUROCHEMISTRY, 2005, 94 (01) :192-203
[9]   Site-specific monoubiquitination activates Ras by impeding GTPase-activating protein function [J].
Baker, Rachael ;
Lewis, Steven M. ;
Sasaki, Atsuo T. ;
Wilkerson, Emily M. ;
Locasale, Jason W. ;
Cantley, Lewis C. ;
Kuhlman, Brian ;
Dohlman, Henrik G. ;
Campbell, Sharon L. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2013, 20 (01) :46-U62
[10]   Prevention of Experimental Colitis by a Selective Inhibitor of the Immunoproteasome [J].
Basler, Michael ;
Dajee, Maya ;
Moll, Carlo ;
Groettrup, Marcus ;
Kirk, Christopher J. .
JOURNAL OF IMMUNOLOGY, 2010, 185 (01) :634-641