PI3K/AKT/mTOR通路
蛋白激酶B
转移
癌症研究
癌症
基因沉默
增强子
基因敲除
磷酸化
生物
信号转导
细胞生物学
基因表达
基因
遗传学
作者
Yong Jae Jin,Ying Xia,Hong Du,T. Xiang,Bingxue Lan,Sixi Wei,Hongyu Li,Hai Huang
标识
DOI:10.1016/j.bbrc.2023.149188
摘要
This study focused on exploring the mechanism of the EMT mediated by endonuclease/exonuclease/phosphatase family domain-containing 1 (EEPD1) in gastric cancer metastasis. Through bioinformatics analysis, EEPD1 was found to be a target gene of super enhancers (SEs) in gastric cancer tissues. EEPD1 exhibited higher expression levels in tumor tissues and was associated with poor prognosis. In vitro and in vivo studies have demonstrated that silencing EEPD1 significantly suppressed the proliferation, metastasis, and invasion of gastric cancer cells. Furthermore, EEPD1 knockdown was involved in the regulation of the EMT and suppressed expression of AKT, a downstream component of the PI3K pathway, leading to a reduction in the phosphorylation levels of AKT and its downstream molecule, mTOR. These results showed the potential of EEPD1 as a prognostic indicator and therapeutic target in gastric cancer.
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