» Articles » PMID: 30827998

Potential Anticancer Activity of Auranofin

Overview
Specialties Chemistry
Pharmacology
Date 2019 Mar 5
PMID 30827998
Citations 45
Authors
Affiliations
Soon will be listed here.
Abstract

Gold compounds have a long history of use in medicine. Auranofin was developed more than 30 years ago as an oral therapy for rheumatoid arthritis. Now, however, auranofin is rarely used in clinical practice despite its efficacy for treating rheumatoid arthritis because more novel antirheumatic medications are available. Although its use in clinical practice has decreased, studies on auranofin have continued and it shows promise for the treatment of several different diseases, including cancer and bacterial and parasitic infections. Several potential novel applications of auranofin for treating human disease have been proposed. Auranofin inhibits the activity of thioredoxin reductase (TrxR), an enzyme of the thioredoxin (Trx) system that is important for maintaining the intracellular redox state. Particularly in cancers, TrxR inhibition leads to an increase in cellular oxidative stress and induces apoptosis. TrxR overexpression is associated with aggressive tumor progression and poor survival in patients with breast, ovarian, and lung cancers. The Trx system may represent an attractive target for the development of new cancer treatments. Therefore, the TrxR inhibitor auranofin may be a potent anticancer agent. This review summarizes the current understanding of auranofin for cancer therapy.

Citing Articles

Inhibition of Thioredoxin-Reductase by Auranofin as a Pro-Oxidant Anticancer Strategy for Glioblastoma: In Vitro and In Vivo Studies.

Chmelyuk N, Kordyukova M, Sorokina M, Sinyavskiy S, Meshcheryakova V, Belousov V Int J Mol Sci. 2025; 26(5).

PMID: 40076706 PMC: 11900239. DOI: 10.3390/ijms26052084.


Gold(I) Complexes Based on Nonsteroidal Anti-Inflammatory Derivatives as Multi-Target Drugs against Colon Cancer.

Saez J, Quero J, Rodriguez-Yoldi M, Gimeno M, Cerrada E Inorg Chem. 2024; 63(42):19769-19782.

PMID: 39389034 PMC: 11497205. DOI: 10.1021/acs.inorgchem.4c02988.


Auranofin is active against Histoplasma capsulatum and reduces the expression of virulence-related genes.

Almeida M, Baeza L, Silva L, Bernardes-Engemann A, Almeida-Silva F, Coelho R PLoS Negl Trop Dis. 2024; 18(10):e0012586.

PMID: 39374315 PMC: 11495550. DOI: 10.1371/journal.pntd.0012586.


Anticancer Activity of Metallodrugs and Metallizing Host Defense Peptides-Current Developments in Structure-Activity Relationship.

Andres C, Perez de la Lastra J, Munguira E, Juan C, Perez-Lebena E Int J Mol Sci. 2024; 25(13).

PMID: 39000421 PMC: 11242492. DOI: 10.3390/ijms25137314.


The thioredoxin system determines CHK1 inhibitor sensitivity via redox-mediated regulation of ribonucleotide reductase activity.

Prasad C, Oo A, Liu Y, Qiu Z, Zhong Y, Li N Nat Commun. 2024; 15(1):4667.

PMID: 38821952 PMC: 11143221. DOI: 10.1038/s41467-024-48076-9.