脂肪甘油三酯脂肪酶
脂解
乳腺癌
癌症研究
转移
脱氮酶
内科学
癌症
磷酸化
泛素
内分泌学
医学
生物
化学
脂肪组织
细胞生物学
生物化学
基因
作者
Yuanzhang Zhou,Peng Chu,Ya Wang,Na Li,Qiong Gao,Shengnan Wang,Juncheng Wei,Guoqing Xue,Yue Zhao,Huijun Jia,Jiankun Song,Yue Zhang,Yu-Qiao Pang,Houyu Zhu,Jia Sun,Suxian Ma,Chen Su,Bingjin Hu,Zhuoyue Zhao,Hui Zhang
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2024-08-16
卷期号:10 (33)
被引量:9
标识
DOI:10.1126/sciadv.ado1533
摘要
Chronic stress–induced epinephrine (EPI) accelerates breast cancer progression and metastasis, but the molecular mechanisms remain unclear. Herein, we found a strong positive correlation between circulating EPI levels and the tumoral expression of ubiquitin-specific peptidase 22 (USP22) in patients with breast cancer. USP22 facilitated EPI-induced breast cancer progression and metastasis by enhancing adipose triglyceride lipase (ATGL)–mediated lipolysis. Targeted USP22 deletion decreased ATGL expression and lipolysis, subsequently inhibiting EPI-mediated breast cancer lung metastasis. USP22 acts as a bona fide deubiquitinase for the Atgl gene transcription factor FOXO1, and EPI architects a lipolysis signaling pathway to stabilize USP22 through AKT-mediated phosphorylation. Notably, USP22 phosphorylation levels are positively associated with EPI and with downstream pathways involving both FOXO1 and ATGL in breast cancers. Pharmacological USP22 inhibition synergized with β-blockers in treating preclinical xenograft breast cancer models. This study reveals a molecular pathway behind EPI’s tumor-promoting effects and provides a strong rationale for combining USP22 inhibition with β-blockers to treat aggressive breast cancer.
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