下调和上调
基因敲除
肾上腺素
癌症研究
调节器
肝细胞癌
信号转导
肿瘤进展
内科学
细胞生物学
化学
医学
生物
癌症
基因
生物化学
作者
Chen Wang,Jiaping Ni,Dayong Zhai,Yanchao Xu,Zijie Wu,Yuyuan Chen,Ning Liu,Juan Du,Yumeng Shen,Guilai Liu,Yong Yang,Linjun You,Weiwei Hu
标识
DOI:10.1038/s12276-024-01223-0
摘要
Hepatocellular carcinoma (HCC) is associated with a poor prognosis. Our previous study demonstrated that Pleomorphic adenoma gene like-2 (PLAGL2) was a potential therapeutic target in HCC. However, the mechanisms that lead to the upregulation of PLAGL2 in HCC remain unclear. The present study revealed that stress-induced epinephrine increased the expression of PLAGL2, thereby promoting the progression of HCC. Furthermore, PLAGL2 knockdown inhibited epinephrine-induced HCC development. Mechanistically, epinephrine upregulated ubiquitin-specific protease 10 (USP10) to stabilize PLAGL2 via the adrenergic β-receptor-2-c-Myc (ADRB2-c-Myc) axis. Furthermore, PLAGL2 acted as a transcriptional regulator of USP10, forming a signaling loop. Taken together, these results reveal that stress-induced epinephrine activates the PLAGL2-USP10 signaling loop to enhance HCC progression. Furthermore, PLAGL2 plays a crucial role in psychological stress-mediated promotion of HCC progression.
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