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Ferroptosis and cuproptosis: Metal-dependent cell death pathways activated in response to classical chemotherapy – Significance for cancer treatment?

Mateusz Kciuk, Adrianna Gielecińska, Żaneta Kałuzińska‐Kołat, Esam Bashir Yahya, Renata Kontek

2024Biochimica et Biophysica Acta (BBA) - Reviews on Cancer37 citationsDOIOpen Access PDF

Abstract

Apoptosis has traditionally been regarded as the desired cell death pathway activated by chemotherapeutic drugs due to its controlled and non-inflammatory nature. However, recent discoveries of alternative cell death pathways have paved the way for immune-stimulatory treatment approaches in cancer. Ferroptosis (dependent on iron) and cuproptosis (dependent on copper) hold promise for selective cancer cell targeting and overcoming drug resistance. Copper ionophores and iron-bearing nano-drugs show potential for clinical therapy as single agents and as adjuvant treatments. Here we review up-to-date evidence for the involvement of metal ion-dependent cell death pathways in the cytotoxicity of classical chemotherapeutic agents (alkylating agents, topoisomerase inhibitors, antimetabolites, and mitotic spindle inhibitors) and their combinations with cuproptosis and ferroptosis inducers, indicating the prospects, advantages, and obstacles of their use.

Topics & Concepts

Programmed cell deathCancer cellCytotoxicityApoptosisCancer researchTopoisomeraseCellChemotherapeutic drugsImmunogenic cell deathAdjuvantCancerChemistryBiologyPharmacologyImmunologyBiochemistryEnzymeIn vitroGeneticsFerroptosis and cancer prognosisDrug Transport and Resistance MechanismsCancer, Lipids, and Metabolism
Ferroptosis and cuproptosis: Metal-dependent cell death pathways activated in response to classical chemotherapy – Significance for cancer treatment? | Litcius