Cuproptosis: a novel therapeutic target for overcoming cancer drug resistance

Elsevier

Available online 11 November 2023, 101018

Drug Resistance UpdatesAuthor links open overlay panel, , , , , , , , , Abstract

Cuproptosis is a newly identified form of cell death driven by copper. Recently, the role of copper and copper triggered cell death in the pathogenesis of cancers have attracted attentions. Cuproptosis has garnered enormous interest in cancer research communities because of its great potential for cancer therapy. Copper-based treatment exerts an inhibiting role in tumor growth and may open the door for the treatment of chemotherapy-insensitive tumors. In this review, we provide a critical analysis on copper homeostasis and the role of copper dysregulation in the development and progression of cancers. Then the core molecular mechanisms of cuproptosis and its role in cancer is discussed, followed by summarizing the current understanding of copper-based agents (copper chelators, copper ionophores, and copper complexes-based dynamic therapy) for cancer treatment. Additionally, we summarize the emerging data on copper complexes-based agents and copper ionophores to subdue tumor chemotherapy resistance in different types of cancers. We also review the small-molecule compounds and nanoparticles (NPs) that may kill cancer cells by inducing cuproptosis, which will shed new light on the development of anticancer drugs through inducing cuproptosis in the future. Finally, the important concepts and pressing questions of cuproptosis in future research that should be focused on were discussed. This review article suggests that targeting cuproptosis could be a novel antitumor therapy and treatment strategy to overcome cancer drug resistance.

AbbreviationsALDH2

aldehyde dehydrogenase 2

ATOX1

copper chaperone antioxidant 1 copper chaperone

ATP7B

copper exporter ATPase copper transporting beta

CCS

Cu chaperone for superoxide dismutase

CTR1

Cu transport protein 1

DCYTB

duodenal cytochrome b

DLAT

lipoylated dihydrolipoamide S-acetyltransferase

DMT1

divalent metal transporter 1

EMT

epithelial-to-mesenchymal transition

IMS

mitochondrial intermembrane space

MEMO1

Mediator of ErbB2-driven cell Motility

OXPHOS

oxidative phosphorylation

SCO1

synthesis of cytochrome C oxidase 1

SLC25A3

solute carrier family 25 member 3

STEAP

six-transmembrane epithelial antigen of the prostate

TCA

mitochondrial tricarboxylic acid

TTM

copper chelator ammonium tetrathiomolybdate

Keywords

Cuproptosis

Cancer

Copper

Drug resistance

Nanoparticles

© 2023 The Author(s). Published by Elsevier Ltd.

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