Monitoring the Action of Redox-directed Cancer Therapeutics Using a Human Peroxiredoxin-2-based Probe
Overview
Affiliations
Redox cancer therapeutics target the increased reliance on intracellular antioxidant systems and enhanced susceptibility to oxidant-induced stress of some cancer cells compared to normal cells. Many of these therapeutics are thought to perturb intracellular levels of the oxidant hydrogen peroxide (HO), a signaling molecule that modulates a number of different processes in human cells. However, fluorescent probes for this species remain limited in their ability to detect the small perturbations induced during successful treatments. We report a fluorescent sensor based upon human peroxiredoxin-2, which acts as the natural indicator of small HO fluctuations in human cells. The new probe reveals peroxide-induced oxidation in human cells below the detection limit of current probes, as well as peroxiredoxin-2 oxidation caused by two different redox cancer therapeutics in living cells. This capability will be useful in elucidating the mechanism of current redox-based therapeutics and in developing new ones.
Measurement of Mitochondrial ROS Formation.
Mena D, Arusei R, Rahhali K, Di Lisa F, Kaludercic N Methods Mol Biol. 2024; 2878():99-116.
PMID: 39546259 DOI: 10.1007/978-1-0716-4264-1_6.
Genetically Encoded Biosensors for the Fluorescence Detection of O and Reactive O Species.
Marchetti M, Ronda L, Cozzi M, Bettati S, Bruno S Sensors (Basel). 2023; 23(20).
PMID: 37896609 PMC: 10611200. DOI: 10.3390/s23208517.
Cuproptosis predicts the risk and clinical outcomes of lung adenocarcinoma.
Hu Q, Wang R, Ma H, Zhang Z, Xue Q Front Oncol. 2022; 12:922332.
PMID: 36003780 PMC: 9393616. DOI: 10.3389/fonc.2022.922332.
Lee J, Lee H, Kim H, Yun J, Lee T, Lee G Mater Today Bio. 2022; 14:100241.
PMID: 35313446 PMC: 8933517. DOI: 10.1016/j.mtbio.2022.100241.
Mitochondria-Targeting Chemodynamic Therapy Nanodrugs for Cancer Treatment.
Chen Q, Li N, Wang X, Yang Y, Xiang Y, Long X Front Pharmacol. 2022; 13:847048.
PMID: 35222052 PMC: 8866723. DOI: 10.3389/fphar.2022.847048.