SOX2
肺癌
基因敲除
癌症干细胞
癌症研究
下调和上调
信使核糖核酸
生物
核糖核酸
长非编码RNA
肺
分子生物学
化学
细胞生物学
干细胞
医学
转录因子
内科学
病理
细胞培养
基因
遗传学
生物化学
作者
You Lü,Jing Cheng,Qixing Mao,Zhongqiu Wang,Qiang Wei
摘要
Abstract The roles of long non‐coding RNA TDRG1 have been revealed in several tumors, especially its roles in CSC progression have been recently elucidated; However, its effects in lung CSC progression have not been revealed. In the present study, we collected 3D non‐adherent spheres as the CSC model to measure lncRNA TDRG1 level in lung CSC and the parental lung cancer cells, and found that TDRG1 level was significantly upregulated in lung CSCs compared to that of parental lung cancer cells. Then we constructed the lung CSCs with or without TDRG1 stable knockdown and lung cancer cells with or without TDRG1 stable overexpression. It was found that TDRG1 positively regulated lung cancer stemness. Mechanistically, we identified that TDRG1 directly bound to Sox2 mRNA, which is a critical stemness regulator, enhanced its mRNA stability, and thus increased Sox2 expression. Indeed, we demonstrated that TDRG1 aggravated lung cancer stemness dependent on Sox2 expression. Thus, this study suggests that TDRG1 is a critical stemness promoter of lung cancer cells by acting as a stabilizer for Sox2 mRNA.
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