癌症研究
染色质免疫沉淀
化学
转录因子
细胞凋亡
体内
流式细胞术
脂质过氧化
活性氧
细胞毒性
药理学
分子生物学
生物
基因表达
氧化应激
发起人
体外
生物化学
生物技术
基因
标识
DOI:10.3389/fcell.2025.1637767
摘要
Alisertib is identified as a potent enhancer of Donafenib-induced ferroptosis through inhibition of the NF-κB/NRF2 pathway. This suggests a novel combinatorial strategy that targets ferroptosis through NF-κB inhibition. Further research is needed to translate these promising results into clinical practice.
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