Ubiquitination and deubiquitination: Implications on cancer therapy

被引:35
|
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
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.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] Anaphase initiation is regulated by antagonistic ubiquitination and deubiquitination activities
    Frank Stegmeier
    Michael Rape
    Viji M. Draviam
    Grzegorz Nalepa
    Mathew E. Sowa
    Xiaolu L. Ang
    E. Robert McDonald III
    Mamie Z. Li
    Gregory J. Hannon
    Peter K. Sorger
    Marc W. Kirschner
    J. Wade Harper
    Stephen J. Elledge
    Nature, 2007, 446 : 876 - 881
  • [32] Regulation of TGF-β family signalling by ubiquitination and deubiquitination
    Imamura, Takeshi
    Oshima, Yusuke
    Hikita, Atsuhiko
    JOURNAL OF BIOCHEMISTRY, 2013, 154 (06): : 481 - 489
  • [33] Ubiquitination and deubiquitination of PCNA in response to stalling of the replication fork
    Brown, Stephanie
    Niimi, Atsuko
    Lehmann, Alan R.
    CELL CYCLE, 2009, 8 (05) : 689 - 692
  • [34] The role and advance of ubiquitination and deubiquitination in depression pathogenesis and treatment
    Yan, Xiaoru
    Ma, Yunhui
    Yang, Junting
    Chang, Xiaoqi
    Shi, Shuxuan
    Song, Guohua
    DRUG DEVELOPMENT RESEARCH, 2024, 85 (07)
  • [35] Controlling ion channel trafficking by targeted ubiquitination and deubiquitination
    Morgenstern, Travis J.
    Colecraft, Henry M.
    ION CHANNELS: CHANNEL CHEMICAL BIOLOGY, ENGINEERING, AND PHYSIOLOGICAL FUNCTION, 2021, 654 : 139 - 167
  • [36] Ubiquitination and Deubiquitination of G Protein-Coupled Receptors
    Jean-Charles, P. -Y.
    Snyder, J. C.
    Shenoy, S. K.
    UBIQUITINATION AND TRANSMEMBRANE SIGNALING, 2016, 141 : 1 - 55
  • [37] UBIQUITINATION AND DEUBIQUITINATION OF DNA REPAIR FACTORS: MODULATION BY MODIFICATION
    He, J.
    Zhu, Q.
    Wani, G.
    Sharma, N.
    Han, C.
    Qian, J.
    Pentz, K.
    Wang, Q.
    Wani, A. A.
    ANTICANCER RESEARCH, 2014, 34 (10) : 6241 - 6241
  • [38] Anaphase initiation is regulated by antagonistic ubiquitination and deubiquitination activities
    Stegmeier, Frank
    Rape, Michael
    Draviam, Viji M.
    Nalepa, Grzegorz
    Sowa, Mathew E.
    Ang, Xiaolu L.
    McDonald, E. Robert, III
    Li, Mamie Z.
    Hannon, Gregory J.
    Sorger, Peter K.
    Kirschner, Marc W.
    Harper, J. Wade
    Elledge, Stephen J.
    NATURE, 2007, 446 (7138) : 876 - 881
  • [39] To Ub or not to Ub: Regulation of circadian clocks by ubiquitination and deubiquitination
    Srikanta, Shashank Bangalore
    Cermakian, Nicolas
    JOURNAL OF NEUROCHEMISTRY, 2021, 157 (01) : 11 - 30
  • [40] Regulation of Wnt Signaling through Ubiquitination and Deubiquitination in Cancers
    Park, Hong-Beom
    Kim, Ju-Won
    Baek, Kwang-Hyun
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (11) : 1 - 28