IκB激酶
激活剂(遗传学)
磷酸化
激酶
信号转导
细胞生物学
STAT蛋白
蛋白激酶B
贾纳斯激酶
肿瘤坏死因子α
化学
生物
NF-κB
车站3
受体
生物化学
免疫学
作者
Jaehwi Lee,Man Hee Rhee,Eunji Kim,Jae Youl Cho
摘要
BAY 11-7082 (BAY) is an inhibitor of κ B kinase (IKK) that has pharmacological activities that include anticancer, neuroprotective, and anti-inflammatory effects. In this study, BAY-pharmacological target pathways were further characterized to determine how this compound simultaneously suppresses various responses. Primary and cancerous (RAW264.7 cells) macrophages were activated by lipopolysaccharide, a ligand of toll-like receptor 4. As reported previously, BAY strongly suppressed the production of nitric oxide, prostaglandin E 2 , and tumor necrosis factor- α and reduced the translocation of p65, major subunit of nuclear factor- κ B, and its upstream signaling events such as phosphorylation of I κ B α , IKK, and Akt. In addition, BAY also suppressed the translocation and activation of activator protein-1, interferon regulatory factor-3, and signal transducer and activator of transcription-1 by inhibiting the phosphorylation or activation of extracellular signal-related kinase, p38, TANK-binding protein, and Janus kinase-2. These data strongly suggest that BAY is an inhibitor with multiple targets and could serve as a lead compound in developing strong anti-inflammatory drugs with multiple targets in inflammatory responses.
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