Auranofin and its analogs as prospective agents for the treatment of colorectal cancer

Lara Massai , Damiano Cirri , Tiziano Marzo , Luigi Messori

Cancer Drug Resistance ›› 2022, Vol. 5 ›› Issue (1) : 1 -14.

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Cancer Drug Resistance ›› 2022, Vol. 5 ›› Issue (1) :1 -14. DOI: 10.20517/cdr.2021.71
review-article

Auranofin and its analogs as prospective agents for the treatment of colorectal cancer

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Abstract

Today colorectal cancer (CRC) is one of the leading causes of cancer death worldwide. This disease is poorly chemo-sensitive toward the existing medical treatments so that new and more effective therapeutic agents are urgently needed and intensely sought. Platinum drugs, oxaliplatin in particular, were reported to produce some significant benefit in CRC treatment, triggering the general interest of medicinal chemists and oncologists for metal-based compounds as candidate anti-CRC drugs. Within this frame, gold compounds and, specifically, the established antiarthritic drug auranofin with its analogs, form a novel group of promising anticancer agents. Owing to its innovative mechanism of action and its favorable pharmacological profile, auranofin together with its derivatives are proposed here as novel experimental agents for CRC treatment, capable of overcoming resistance to platinum drugs. Some encouraging results in this direction have already been obtained. A few recent studies demonstrate that the action of auranofin may be further potentiated through the preparation of suitable pharmaceutical formulations capable of protecting the gold pharmacophore from unselective reactivity or through the design of highly synergic drug combinations. The perspectives of the research in this field are outlined.

Keywords

Auranofin / CRC / colorectal cancer / metallodrugs / anticancer agents / gold / gold-based drugs

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Lara Massai, Damiano Cirri, Tiziano Marzo, Luigi Messori. Auranofin and its analogs as prospective agents for the treatment of colorectal cancer. Cancer Drug Resistance, 2022, 5(1): 1-14 DOI:10.20517/cdr.2021.71

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