MAPK/ERK通路
PI3K/AKT/mTOR通路
糖酵解
体内
缺氧诱导因子1
癌症研究
转录因子
生物
缺氧(环境)
药理学
缺氧诱导因子
磷酸化
化学
信号转导
细胞生物学
生物化学
酶
基因
生物技术
有机化学
氧气
作者
Zhiyuan Zheng,Xu Tian,Zhiyan Liu,Wenyue Tian,Zhihong Jiang,Guo‐Yuan Zhu,Ting Li,Jin Gao,Liping Bai
标识
DOI:10.1016/j.biopha.2022.113319
摘要
As a characteristic transcription factor in solid tumors, hypoxia inducible factor-1 (HIF-1) acts as a master regulator in breast cancer progression. Cryptolepine, as a natural alkaloid, noticeably inhibited HIF-1 transcriptional activity and decreased the protein expression of hypoxia-induced HIF-1α in breast cancer cells. Further study showed that cryptolepine blocked HIF-1-mediated glycolysis and suppressed the expression of multiple glycolysis enzymes, resulting in a decrease in ATP production in hypoxic T47D and 4T1 cells. Meanwhile, cryptolepine displayed potent suppressive effect on tumor growth in a dose-dependent manner. In 4T1 tumor xenografts, cryptolepine reduced HIF-1α protein expression, and thus decreased the levels of both lactate acid and ATP productions. The mechanistic study revealed that cryptolepine could effectively suppress the process of HIF-1α mRNA translation rather than transcription, which was attributed to the inhibition on the phosphorylation of eIF4E regulated by both MAPK and mTOR signaling pathways. Collectively, current findings suggested that cryptolepine possesses the potential to treat breast cancers by modulating HIF-1 both in vitro and in vivo.
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