SOX2
生物
CD44细胞
癌症研究
肺癌
A549电池
分子生物学
细胞凋亡
细胞
胚胎干细胞
病理
遗传学
医学
基因
作者
Shuanglong Xiong,Donglin Wang,Yin Tang,Songmei Lu,Lumi Huang,Zhi‐Juan Wu,Shuangyi Lei,Guanzhong Liang,Dan Yang,Dairong Li,Yan Li
出处
期刊:Gene
[Elsevier]
日期:2023-02-16
卷期号:863: 147288-147288
被引量:7
标识
DOI:10.1016/j.gene.2023.147288
摘要
To explore HIF1α and HIF2α regulate the dedifferentiation of lung cancer cells under hypoxic conditions through Sox2 and Oct4.HIF1α, HIF2α, Sox2 and Oct4 expression was analysed in lung cancer tissues. We analysed sphere formation by single-cell of differentiated lung cancer under hypoxia, and detected the expression of CD133, CD44, Sox2, Oct4, HIF1α and HIF2α. We knocked out HIF1α, HIF2α, Sox2 or Oct4 in cells, cultured the cells under hypoxic conditions and detected CD133 and CD44 using western blotting. We also detected the apoptosis rate of cells with HIF1α, HIF2α, Sox2 or Oct4 knockout.There was more sphere formation of differentiated lung cancer cells under hypoxic conditions than of control cells under normoxic conditions. These newly formed spheres highly expressed CD133 and CD44. TCGA database showed high expression of HIF1α and HIF2α in lung cancer tissues. After knocking out HIF1α and HIF2α, the expression of Sox2, Oct4, CD133 and CD44 decreased significantly, and after knocking out Sox2 or Oct4, the expression of CD133 and CD44 decreased.HIF1α and HIF2α regulate non-small-cell lung cancer dedifferentiation through Sox2 and Oct4 under hypoxic conditions.
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