Abstract:
Glutathione S-transferase (GST
π), one of the phase Ⅱ detoxification enzymes, is usually over-expressed in many human tumors. It displays a key role in protecting cells through catalyzing the conjugation of glutathione (GSH) with a broad range of electrophilic substrates including chemotherapeutic agents. As the above conjugates can be effluxed from cells easily, the efficacy of various chemotherapeutic agents is reduced. Recent studies suggest that GST
π also plays an important role in inhibiting apoptosis through blocking the JNK signaling pathway. In this way, GST
π protects cells from apoptosis. Therefore, GST
π has become an attractive target against cancers, especially for drug-resistant tumors. A great deal of effort has been devoted to the discovery of GST
π inhibitors and prodrugs over the last decade. In connection with authors' current research, we provide a review on studies on progress of GST
π inhibitors and prodrugs along with the future strategies.