化学
亚精胺
MAPK/ERK通路
信号转导
细胞生物学
过氧化脂质
精胺
活性氧
转录因子
脂质过氧化
氧化应激
基因
生物化学
生物
酶
作者
Zhou Liu,Hongjin Chen,Yingnan Song,Kaiyuan Chen,Sisi Pan,Siyuan Yang,Deqin Lu
标识
DOI:10.3389/fphar.2024.1476718
摘要
In sum, this study demonstrated Sat1 expression was increased in MIRI, inhibition of Sat1 can alleviate MIRI by regulating ferroptosis via MAPK/ERK pathway, and Sat1 was negatively regulated by Sox2. These findings suggested that Sat1 may serve as a potential therapeutic target for the treatment of MIRI.
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