医学
RNA干扰
NF-κB
蛋白酶体
转录因子
药品
IκB激酶
癌症治疗
癌症研究
药理学
生物信息学
计算生物学
癌症
基因
核糖核酸
免疫学
生物
内科学
遗传学
炎症
作者
Derek J. Erstad,James C. Cusack
标识
DOI:10.1016/j.soc.2013.06.011
摘要
Most NF-κB inhibitors target the IKK complex, IκB proteins, or NF-κB transcription factors. The most promising classes of inhibitors include antioxidants, antiinflammatory compounds, natural compounds, statins, proteasome inhibitors, IKKβ inhibitors, biologics, gene therapy, and RNA interference. Targeting NF-κB is limited by intrinsic pathway complexity, cross-talk with other pathways, a lack of biomarkers, poor drug specificity, drug resistance, and difficulty with drug delivery. Future NF-κB targeting will be improved through better understanding of the pathway, more specific inhibitors, and multimodality therapies.
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