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  • Lipid-derived electrophiles mediate the effects of chemotherapeutic topoisomerase I poisons.

Lipid-derived electrophiles mediate the effects of chemotherapeutic topoisomerase I poisons.

Cell chemical biology (2020-12-23)
Amy Flor, Donald Wolfgeher, Jing Li, Leslyn A Hanakahi, Stephen J Kron
ABSTRACT

Topoisomerase 1 (Top1) reversibly nicks chromosomal DNA to relax strain accumulated during transcription, replication, chromatin assembly, and chromosome condensation. The Top1 poison camptothecin targets cancer cells by trapping the enzyme in the covalent complex Top1cc, tethered to cleaved DNA by a tyrosine-3'-phosphate bond. In vitro mechanistic studies point to interfacial inhibition, where camptothecin binding to the Top1-DNA interface stabilizes Top1cc. Here we present a complementary covalent mechanism that is critical in vivo. We observed that camptothecins induce oxidative stress, leading to lipid peroxidation, lipid-derived electrophile accumulation, and Top1 poisoning via covalent modification. The electrophile 4-hydroxy-2-nonenal can induce Top1cc on its own and forms a Michael adduct to a cysteine thiol in the Top1 active site, potentially blocking tyrosine dephosphorylation and 3' DNA phosphate release. Thereby, camptothecins may leverage a physiological cysteine-based redox switch in Top1 to mediate their selective toxicity to rapidly proliferating cancer cells.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
AldeRed® ALDH Detection Assay
Sigma-Aldrich
Anti-Topoisomerase I-DNA Covalent Complexes Antibody, clone 1.1A, clone 1.1A, from mouse