Table 3.
Therapeutic treatments targeting the NF-κB pathway.
Target in the NF-κB pathway | compounds | type | Mechanism of action | Ref. |
---|---|---|---|---|
NF-κB | Glucocorticoids | Anti-inflammatory | Binds to NF-κB and prevents transactivation. Induces transcription and synthesis of IκBα | (244, 245) |
IKK | sulfasalazine | Anti-inflammatory | Inhibits IKKα and β activation | (246) |
P65 | Mesalamine | Anti-inflammatory | Inhibits IOL-1mediated p65 phosphorylation | (247) |
IκBα | Aspirine (high dose) | Anti-inflammatory | Prevents IκBα degradation and suppresses NF-κB-dependent transcription | (248) |
IL-1 | Anakinra | Recombinant IL-1Rα | Prevents binding of IL-1β to its receptor | (249) |
TNF-α | Adalimumab | Recombinant IgG1 mAb | Binds to TNF-α and prevent it to activate its receptor | (249) |
IKKβ | SPC-839 | Antiinflammatory | IKKβ inhibitor | (250) |
IKKβ | ML120B | Antiinflammatory | IKKβ inhibitor | (251) |
NF-κB | TPCA1 | Antiinflammatory | Inhibits NF-κB and STAT3 | (252) |
RANKL | DTCM-glutarimide | Antiinflammatory | RANKL inhibitor | (253) |
IKKα and IKKβ | BMS-345541 | Antiinflammatory | IKKα and IKKβ inhibitor | (254) |
NEMO | NEMO antagonist peptides | Peptides | (255) | |
Proteasome | Bortezomib | Cytotoxic agent (cell cycle arrest and apoptosis) | Proteasome inhibitor | (256) |
Immunoproteasome | KZR-616 | Immunoproteasome inhibitor | (257) | |
NF-κB | ODNi | Oligodeoxynucleotides | Inhibits binding of NF-κB to DNA | (255) |