Ubiquitination and deubiquitination: Implications on cancer therapy

被引:55
作者
Dagar, Gunjan [1 ]
Kumar, Rakesh [2 ]
Yadav, Kamlesh K. [3 ,4 ]
Singh, Mayank [1 ]
Pandita, Tej K. [3 ]
机构
[1] All India Inst Med Sci, Dept Med Oncol, Dr BRAIRCH, New Delhi 110029, India
[2] Shri Mata Vaishno Devi Univ, Sch Biotechnol, Katra 182320, Jammu & Kashmir, India
[3] Texas A&M Coll Med, Ctr Genom & Precis Med, Houston, TX 77030 USA
[4] Texas A&M Univ, Sch Engn Med, Sch Med, Houston, TX 77030 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE REGULATORY MECHANISMS | 2023年 / 1866卷 / 04期
关键词
Ubiquitin proteasomal system (UPS); Deubiquitin enzymes (DUBs); Ubiquitin ligase; DNA damage; PROTEASOME SYSTEM; EPIGENETIC INACTIVATION; GENOME STABILITY; DNA-REPLICATION; P53; RESTORATION; REPAIR; PCNA; ENZYME; PROTEIN; CHFR;
D O I
10.1016/j.bbagrm.2023.194979
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
The ubiquitin proteasomal system (UPS) represents a highly regulated protein degradation pathway essential for maintaining cellular homeostasis. This system plays a critical role in several cellular processes, which include DNA damage repair, cell cycle checkpoint control, and immune response regulation. Recently, the UPS has emerged as a promising target for cancer therapeutics due to its involvement in oncogenesis and tumor progression. Here we aim to summarize the key aspects of the UPS and its significance in cancer therapeutics. We begin by elucidating the fundamental components of the UPS, highlighting the role of ubiquitin, E1-E3 ligases, and the proteasome in protein degradation. Furthermore, we discuss the intricate process of ubiquitination and proteasomal degradation, emphasizing the specificity and selectivity achieved through various signaling pathways. The dysregulation of the UPS has been implicated in cancer development and progression. Aberrant ubiquitin-mediated degradation of key regulatory proteins, such as tumor suppressors and oncoproteins, can lead to uncontrolled cell proliferation, evasion of apoptosis, and metastasis. We outline the pivotal role of the UPS in modulating crucial oncogenic pathways, including the regulation of cyclins, transcription factors, Replication stress components and DNA damage response. The increasing recognition of the UPS as a target for cancer therapeutics has spurred the development of small molecules, peptides, and proteasome inhibitors with the potential to restore cellular balance and disrupt tumor growth. We provide an overview of current therapeutic strategies aimed at exploiting the UPS, including the use of proteasome inhibitors, deubiquitinating enzyme inhibitors, and novel E3 ligase modulators. We further discuss novel emerging strategies for the development of next-generation drugs that target proteasome inhibitors. Exploiting the UPS for cancer therapeutics offers promising avenues for developing innovative and effective treatment strategies, providing hope for improved patient outcomes in the fight against cancer.
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页数:12
相关论文
共 125 条
[1]   The AAA-ATPase VCP/p97 promotes 53BP1 recruitment by removing L3MBTL1 from DNA double-strand breaks [J].
Acs, Klara ;
Luijsterburg, Martijn S. ;
Ackermann, Leena ;
Salomons, Florian A. ;
Hoppe, Thorsten ;
Dantuma, Nico P. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2011, 18 (12) :1345-U55
[2]   JAMM: A metalloprotease-like zinc site in the proteasome and signalosome [J].
Ambroggio, XI ;
Rees, DC ;
Deshaies, RJ .
PLOS BIOLOGY, 2004, 2 (01) :113-119
[3]   Mechanism and function of deubiquitinating enzymes [J].
Amerik, AY ;
Hochstrasser, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1695 (1-3) :189-207
[4]  
Aylon Y., 2007, DYING P53, V130, P597
[5]   Living with p53, dying of p53 [J].
Aylon, Yael ;
Oren, Moshe .
CELL, 2007, 130 (04) :597-600
[6]  
Biswas M., 2011, ROLE HISTONE TAILS S, V7
[7]   Role of Histone Tails in Structural Stability of the Nucleosome [J].
Biswas, Mithun ;
Voltz, Karine ;
Smith, Jeremy C. ;
Langowski, Joerg .
PLOS COMPUTATIONAL BIOLOGY, 2011, 7 (12)
[8]   Interplay of replication checkpoints and repair proteins at stalled replication forks [J].
Branzei, Dana ;
Foiani, Marco .
DNA REPAIR, 2007, 6 (07) :994-1003
[9]   Maintaining genome stability at the replication fork [J].
Branzei, Dana ;
Foiani, Marco .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2010, 11 (03) :208-219
[10]   Regulation of the DNA damage response by ubiquitin conjugation [J].
Brinkmann, Kerstin ;
Schell, Michael ;
Hoppe, Thorsten ;
Kashkar, Hamid .
FRONTIERS IN GENETICS, 2015, 6