The Thioredoxin System of Mammalian Cells and Its Modulators

被引:46
作者
Hasan, Aseel Ali [1 ]
Kalinina, Elena [1 ]
Tatarskiy, Victor [2 ]
Shtil, Alexander [3 ]
机构
[1] RUDN Univ, Peoples Friendship Univ Russia, TT Berezov Dept Biochem, 6 Miklukho Maklaya St, Moscow 117198, Russia
[2] Russian Acad Sci, Inst Gene Biol, Lab Mol Oncobiol, 34-5 Vavilov St, Moscow 119334, Russia
[3] Blokhin Natl Med Res Ctr Oncol, Lab Tumor Cell Death, 24 Kashirskoye Shosse, Moscow 115478, Russia
关键词
thioredoxin system; structure and catalytic function; inhibitors and activators; redox regulation; apoptosis; ESCHERICHIA-COLI THIOREDOXIN; OXIDATIVE STRESS; MOLECULAR-MECHANISMS; GLUTATHIONE SYSTEMS; CANCER-CELLS; ACTIVE-SITE; REDUCTASE; APOPTOSIS; ANTICANCER; INHIBITION;
D O I
10.3390/biomedicines10071757
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
Oxidative stress involves the increased production and accumulation of free radicals, peroxides, and other metabolites that are collectively termed reactive oxygen species (ROS), which are produced as by-products of aerobic respiration. ROS play a significant role in cell homeostasis through redox signaling and are capable of eliciting damage to macromolecules. Multiple antioxidant defense systems have evolved to prevent dangerous ROS accumulation in the body, with the glutathione and thioredoxin/thioredoxin reductase (Trx/TrxR) systems being the most important. The Trx/TrxR system has been used as a target to treat cancer through the thiol-disulfide exchange reaction mechanism that results in the reduction of a wide range of target proteins and the generation of oxidized Trx. The TrxR maintains reduced Trx levels using NADPH as a co-substrate; therefore, the system efficiently maintains cell homeostasis. Being a master regulator of oxidation-reduction processes, the Trx-dependent system is associated with cell proliferation and survival. Herein, we review the structure and catalytic properties of the Trx/TrxR system, its role in cellular signaling in connection with other redox systems, and the factors that modulate the Trx system.
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页数:18
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共 131 条
[1]   The Thioredoxin System Is Regulated by the ASK-1/JNK/p38/Survivin Pathway during Germ Cell Apoptosis [J].
Al-Kandari, Nora ;
Fadel, Fatemah ;
Al-Saleh, Farah ;
Khashab, Farah ;
Al-Maghrebi, May .
MOLECULES, 2019, 24 (18)
[2]   Curcumin Induces Apoptosis of Upper Aerodigestive Tract Cancer Cells by Targeting Multiple Pathways [J].
Amin, A. R. M. Ruhul ;
Haque, Abedul ;
Rahman, Mohammad Aminur ;
Chen, Zhuo Georgia ;
Khuri, Fadlo Raja ;
Shin, Dong Moon .
PLOS ONE, 2015, 10 (04)
[3]   Thioredoxin and Hematologic Malignancies [J].
An, Ningfei ;
Kang, Yubin .
REDOX AND CANCER, PT A, 2014, 122 :245-279
[4]   Cell Death by SecTRAPs: Thioredoxin Reductase as a Prooxidant Killer of Cells [J].
Anestal, Karin ;
Prast-Nielsen, Stefanie ;
Cenas, Narimantas ;
Arner, Elias S. J. .
PLOS ONE, 2008, 3 (04)
[5]   Targeting antioxidant pathways with ferrocenylated N-heterocyclic carbene supported gold(I) complexes in A549 lung cancer cells [J].
Arambula, J. F. ;
McCall, R. ;
Sidoran, K. J. ;
Magda, D. ;
Mitchell, N. A. ;
Bielawski, C. W. ;
Lynch, V. M. ;
Sessler, J. L. ;
Arumugam, K. .
CHEMICAL SCIENCE, 2016, 7 (02) :1245-1256
[6]   Focus on mammalian thioredoxin reductases - Important selenoproteins with versatile functions [J].
Arner, Elias S. J. .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2009, 1790 (06) :495-526
[7]   Molecular Mechanisms of Thioredoxin and Glutaredoxin as Hydrogen Donors for Mammalian S Phase Ribonucleotide Reductase [J].
Avval, Farnaz Zahedi ;
Holmgren, Arne .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (13) :8233-8240
[8]   The Functions of Thioredoxin 1 in Neurodegeneration [J].
Awan, Maher Un Nisa ;
Yan, Fang ;
Mahmood, Faisal ;
Bai, Liping ;
Liu, Jingyu ;
Bai, Jie .
ANTIOXIDANTS & REDOX SIGNALING, 2022, 36 (13) :1023-1036
[9]   Evolution of the thioredoxin system as a step enabling adaptation to oxidative stress [J].
Balsera, Monica ;
Buchanan, Bob B. .
FREE RADICAL BIOLOGY AND MEDICINE, 2019, 140 :28-35
[10]   Dual targeting of the thioredoxin and glutathione systems in cancer and HIV [J].
Benhar, Moran ;
Shytaj, Iart Luca ;
Stamler, Jonathan S. ;
Savarino, Andrea .
JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (05) :1630-1639