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Through mechanisms such as inhibition of drug efflux pumps, modulation of metabolic pathways, regulation of miRNAs, and manipulation of key signaling pathways, UA sensitizes cancer cells to drugs like adriamycin, cisplatin, paclitaxel, and sorafenib

However, most of the developed chromophores and fluorophores exhibit poor selectivity between GSH and other thiol compounds in cells, which may cause interference to the test results [10, 15,16,17,18,19]