Thioredoxin-dependent system. Application of inhibitors

J Enzyme Inhib Med Chem. 2021 Dec;36(1):362-371. doi: 10.1080/14756366.2020.1867121.

Abstract

One of the systems responsible for maintaining cellular redox homeostasis is the thioredoxin-dependent system. An equally important function of this system is the regulation of the expression of many proteins by the transcription factor NF-κB or the apoptosis regulating kinase (ASK-1). Since it has been shown that the Trx-dependent system can contribute to both the enhancement of tumour angiogenesis and growth as well as apoptosis of neoplastic cells, the search for compounds that inhibit the level/activity of Trx and/or TrxR and thus modulate the course of the neoplastic process is ongoing. It has been shown that many naturally occurring polyphenolic compounds inactivate elements of the thioredoxin system. In addition, the effectiveness of Trx is inhibited by imidazole derivatives, while the activity of TrxR is reduced by transition metal ions complexes, dinitrohalobenzene derivatives, Michael acceptors, nitrosourea and ebselen. In addition, research is ongoing to identify new selective Trx/TrxR inhibitors.

Keywords: metal ions complexes; polyphenols; redox imbalance; thioredoxin system; thioredoxin-dependent system inhibitors.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / therapeutic use*
  • Benzene Derivatives / chemistry
  • Benzene Derivatives / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / therapeutic use*
  • Gene Expression Regulation, Neoplastic
  • Homeostasis / drug effects
  • Homeostasis / genetics
  • Humans
  • Imidazoles / chemistry
  • Imidazoles / pharmacology
  • Isoindoles / chemistry
  • Isoindoles / pharmacology
  • MAP Kinase Kinase Kinase 5 / genetics
  • MAP Kinase Kinase Kinase 5 / metabolism
  • NF-kappa B / genetics
  • NF-kappa B / metabolism
  • Neoplasms / drug therapy*
  • Neoplasms / enzymology
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Neovascularization, Pathologic / drug therapy*
  • Neovascularization, Pathologic / enzymology
  • Neovascularization, Pathologic / genetics
  • Neovascularization, Pathologic / pathology
  • Nitrosourea Compounds / chemistry
  • Nitrosourea Compounds / pharmacology
  • Organoselenium Compounds / chemistry
  • Organoselenium Compounds / pharmacology
  • Oxidation-Reduction
  • Signal Transduction
  • Structure-Activity Relationship
  • Thioredoxin-Disulfide Reductase / antagonists & inhibitors
  • Thioredoxin-Disulfide Reductase / genetics*
  • Thioredoxin-Disulfide Reductase / metabolism
  • Thioredoxins / antagonists & inhibitors
  • Thioredoxins / genetics*
  • Thioredoxins / metabolism

Substances

  • Antineoplastic Agents
  • Benzene Derivatives
  • Enzyme Inhibitors
  • Imidazoles
  • Isoindoles
  • NF-kappa B
  • Nitrosourea Compounds
  • Organoselenium Compounds
  • ebselen
  • Thioredoxins
  • Thioredoxin-Disulfide Reductase
  • MAP Kinase Kinase Kinase 5
  • MAP3K5 protein, human