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As shown in this review, most reported literature on GSH transporter targeted brain drug delivery systems was developed based on the use of GSH-PEG compared with the diverse ligands available for the transferrin receptor, LDL-receptor and glucose transporter

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showed that (93), tetrandrine can down-regulate the expression or activation of Akt/JNK, MMP-2, MMP-9, and fibrous F-actin and focal adhesion kinase FAK, reduce the expression of migration-related proteins Rac1, Cdc42 and RhoA in MH7A cells, and block the migration and invasion of RA-FLS

The following pathways are among the most studied