SMAD公司
生物
基因敲除
Smad2蛋白
癌症研究
信号转导
磷酸化
肺癌
长非编码RNA
转化生长因子
细胞生物学
核糖核酸
内科学
医学
细胞凋亡
基因
遗传学
作者
Lele Xu,Wenzhong Liu,Tongtong Li,Yuying Hu,Yu Wang,Lijie Huang,Yan Wang,Shujuan Shao,Xuefeng Liu,Qimin Zhan
出处
期刊:Oncogene
[Springer Nature]
日期:2021-04-30
卷期号:40 (20): 3578-3592
被引量:32
标识
DOI:10.1038/s41388-021-01760-2
摘要
TGF-β/Smad signaling pathway plays an important role in EMT during cancer progression. Long non-coding RNAs (lncRNAs) are involved in various behaviors of cancer cells, including EMT. Here, we report a novel lncRNA adjacent to Smad3, named Smad3-associated long non-coding RNA (SMASR). SMASR is downregulated by TGF-β via Smad2/3 in lung cancer cells. Knockdown of SMASR induces EMT and increases the migration and invasion of lung cancer cells. Moreover, knockdown of SMASR promotes the phosphorylation of Smad2/3. Mechanistically, SMASR interacts with Smad2/3 and inhibits the expression of TGFBR1, the TGF-β type I receptor responsible for phosphorylation of Smad2/3, thus leading to inactivation of TGF-β/Smad signaling pathway. Clinically, SMASR is downregulated in lung cancer tissues. Collectively, our findings prove a critical role of SMASR in EMT of lung cancer by forming a negative feedback loop with TGF-β/Smad signaling pathway.
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