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The first publications reported enzyme activity involving displacement of a halide ion from an aromatic compound, resulting in an S-substituted glutathione conjugate ( GSTs were first recognized as enzymes inactivating xenobiotics, in particular electrophilic mutagens and carcinogens, leading to their excretion as mercapturic acids ( An independent set of reports identified a remarkably abundant protein in liver with affinity for carcinogens, steroid hormones, bilirubin and synthetic dyes

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reported reduced resistance to cisplatin, docetaxel, DOX, and 5-FU in drug-resistant cancer cell lines following the application of CRISPR/Cas9 to knock out urokinase plasminogen activator receptor (uPAR), which is overexpressed in several cancers (456)