The gold complex auranofin sensitizes platinum resistant epithelial ovarian cancer cells to cisplatin

Although numerous drugs have been tested to treat ovarian cancer (OC), survival rates remain low as there has been no major improvement from platinum (Pt)-based therapy and there is a high rate of Pt resistance in these tumors. Following several rounds of chemotherapy, OC cells develop Pt-resistance by increasing DNA repair and antioxidant defense mechanisms. This study aimed to design a treatment to combat recurrent stages of OC by repurposing the anti-rheumatic gold complex auranofin (AF). We demonstrate that AF enhances the efficacy of cisplatin (CDDP) in Pt-resistant epithelial OC (EOC) cells. The drug combination enhanced mitochondrial-dependent apoptosis, PARP cleavage, DNA damage, and ROS overproduction. These results suggest the potential to combine AF with CDDP as a strategy to improve CDDP sensitivity in recurrent EOCs.

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Journal
Biochemistry and Biophysics Reports
Published
2025-04-01
DOI
https://doi.org/10.1016/j.bbrep.2025.101996
Primary Topic
Metal complexes synthesis and properties
Type
article
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0.00
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article

The gold complex auranofin sensitizes platinum resistant epithelial ovarian cancer cells to cisplatin

Edith Zorychta, Alicia Alejandra Goyeneche, Benjamin N. Forgie, Abu Shadat Mohammod Noman et al.
Biochemistry and Biophysics Reports
Metal complexes synthesis and properties
article

The gold complex auranofin sensitizes platinum resistant epithelial ovarian cancer cells to cisplatin

Edith Zorychta, Alicia Alejandra Goyeneche, Benjamin N. Forgie, Abu Shadat Mohammod Noman, Carlos M. Telleria, Farah H. Abdalbari
article en

Abstract

Although numerous drugs have been tested to treat ovarian cancer (OC), survival rates remain low as there has been no major improvement from platinum (Pt)-based therapy and there is a high rate of Pt resistance in these tumors. Following several rounds of chemotherapy, OC cells develop Pt-resistance by increasing DNA repair and antioxidant defense mechanisms. This study aimed to design a treatment to combat recurrent stages of OC by repurposing the anti-rheumatic gold complex auranofin (AF). We demonstrate that AF enhances the efficacy of cisplatin (CDDP) in Pt-resistant epithelial OC (EOC) cells. The drug combination enhanced mitochondrial-dependent apoptosis, PARP cleavage, DNA damage, and ROS overproduction. These results suggest the potential to combine AF with CDDP as a strategy to improve CDDP sensitivity in recurrent EOCs.

Biochemistry and Biophysics ReportsVol. 42
McGill University Health Centre (CA), McGill University (CA), University of Chittagong (BD)
Zero hunger, Good health and well-being
Openalex Percentile: Top 91%
Metal complexes synthesis and properties
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The gold complex auranofin sensitizes platinum resistant epithelial ovarian cancer cells to cisplatin — Edith Zorychta, Alicia Alejandra Goyeneche, et al. · Biochemistry and Biophysics Reports (2025) | TGRS Research Map | TGRS