Advances in Deubiquitinating Enzyme Inhibition and Applications in Cancer Therapeutics

被引:119
作者
Antao, Ainsley Mike [1 ]
Tyagi, Apoorvi [1 ]
Kim, Kye-Seong [1 ,2 ]
Ramakrishna, Suresh [1 ,2 ]
机构
[1] Hanyang Univ, Grad Sch Biomed Sci & Engn, Seoul 04763, South Korea
[2] Hanyang Univ, Coll Med, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
cancer therapy; deubiquitinase; DUB inhibitors; USPs phylogenetic tree; signaling pathways; NF-KAPPA-B; SMALL-MOLECULE INHIBITOR; UBIQUITIN-ACTIVATING ENZYME; FINGER PROTEIN A20; CELL-CYCLE ARREST; ACTIVE PROTEASOME INHIBITOR; GENOME-WIDE ASSOCIATION; I CLINICAL-TRIAL; TUMOR-SUPPRESSOR; MULTIPLE-MYELOMA;
D O I
10.3390/cancers12061579
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Since the discovery of the ubiquitin proteasome system (UPS), the roles of ubiquitinating and deubiquitinating enzymes (DUBs) have been widely elucidated. The ubiquitination of proteins regulates many aspects of cellular functions such as protein degradation and localization, and also modifies protein-protein interactions. DUBs cleave the attached ubiquitin moieties from substrates and thereby reverse the process of ubiquitination. The dysregulation of these two paramount pathways has been implicated in numerous diseases, including cancer. Attempts are being made to identify inhibitors of ubiquitin E3 ligases and DUBs that potentially have clinical implications in cancer, making them an important target in the pharmaceutical industry. Therefore, studies in medicine are currently focused on the pharmacological disruption of DUB activity as a rationale to specifically target cancer-causing protein aberrations. Here, we briefly discuss the pathophysiological and physiological roles of DUBs in key cancer-related pathways. We also discuss the clinical applications of promising DUB inhibitors that may contribute to the development of DUBs as key therapeutic targets in the future.
引用
收藏
页码:1 / 36
页数:34
相关论文
共 324 条
[91]   Frequent Mutation of BAP1 in Metastasizing Uveal Melanomas [J].
Harbour, J. William ;
Onken, Michael D. ;
Roberson, Elisha D. O. ;
Duan, Shenghui ;
Cao, Li ;
Worley, Lori A. ;
Council, M. Laurin ;
Matatall, Katie A. ;
Helms, Cynthia ;
Bowcock, Anne M. .
SCIENCE, 2010, 330 (6009) :1410-1413
[92]   Regulation of NF-κB by deubiquitinases [J].
Harhaj, Edward W. ;
Dixit, Vishva M. .
IMMUNOLOGICAL REVIEWS, 2012, 246 :107-124
[93]   Oprozomib in patients with newly diagnosed multiple myeloma [J].
Hari, Parameswaran ;
Matous, Jeffrey V. ;
Voorhees, Peter M. ;
Shain, Kenneth H. ;
Obreja, Mihaela ;
Frye, John ;
Fujii, Hisaki ;
Jakubowiak, Andrzej J. ;
Rossi, Davide ;
Sonneveld, Pieter .
BLOOD CANCER JOURNAL, 2019, 9 (9)
[94]   The p53 pathway: positive and negative feedback loops [J].
Harris, SL ;
Levine, AJ .
ONCOGENE, 2005, 24 (17) :2899-2908
[95]   Phase I Clinical Trial of Marizomib (NPI-0052) in Patients with Advanced Malignancies Including Multiple Myeloma: Study NPI-0052-102 Final Results [J].
Harrison, Simon J. ;
Mainwaring, Paul ;
Price, Timothy ;
Millward, Michael J. ;
Padrik, Peeter ;
Underhill, Craig R. ;
Cannell, Paul K. ;
Reich, Steven D. ;
Trikha, Mohit ;
Spencer, Andrew .
CLINICAL CANCER RESEARCH, 2016, 22 (18) :4559-4566
[96]   Phase II Study of Carfilzomib in Patients With Refractory Renal Cell Carcinoma [J].
Hasanov, Elshad ;
Tidwell, Rebecca S. S. ;
Fernandez, Pablo ;
Park, Lauren ;
McMichael, Charla ;
Tannir, Nizar M. ;
Jonasch, Eric .
CLINICAL GENITOURINARY CANCER, 2019, 17 (06) :451-456
[97]   Inhibition of ubiquitin-specific protease 2 causes accumulation of reactive oxygen species, mitochondria dysfunction, and intracellular ATP decrement in C2C12 myoblasts [J].
Hashimoto, Mayuko ;
Saito, Natsuko ;
Ohta, Haru ;
Yamamoto, Kumiko ;
Tashiro, Asuka ;
Nakazawa, Kosuke ;
Inanami, Osamu ;
Kitamura, Hiroshi .
PHYSIOLOGICAL REPORTS, 2019, 7 (14)
[98]   Curcumin: From ancient medicine to current clinical trials [J].
Hatcher, H. ;
Planalp, R. ;
Cho, J. ;
Tortia, F. M. ;
Torti, S. V. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (11) :1631-1652
[99]   Shared principles in NF-κB signaling [J].
Hayden, Matthew S. ;
Ghosh, Sankar .
CELL, 2008, 132 (03) :344-362
[100]   Discovery of Mdm2-MdmX E3 Ligase Inhibitors Using a Cell-Based Ubiquitination Assay [J].
Herman, Ariel G. ;
Hayano, Miki ;
Poyurovsky, Masha V. ;
Shimada, Kenichi ;
Skouta, Rachid ;
Prives, Carol ;
Stockwell, Brent R. .
CANCER DISCOVERY, 2011, 1 (04) :312-325