蛋白酶体
细胞周期
细胞生长
癌症
肿瘤进展
癌症研究
癌细胞
细胞生物学
调节器
细胞
SKP2型
生物
泛素
遗传学
基因
泛素连接酶
作者
Liyun Zheng,Jiajia Shen,Chen Yang,Jingyu Lin,Pengyu Li,Xiaoli Zhao,Hangjiang Ren,Yi Sun,Zhen Wang
出处
期刊:Cancer Letters
[Elsevier]
日期:2024-04-09
卷期号:591: 216848-216848
被引量:1
标识
DOI:10.1016/j.canlet.2024.216848
摘要
FBXO43 is a member of the FBXO subfamily of F-box proteins, known to be a regulatory hub during meiosis. A body of data showed that FBXO43 is overexpressed in a number of human cancers. However, whether and how FBXO43 affects cell cycle progression and growth of cancer cells remain elusive. In this study, we provide first piece of evidence, showing a pivotal role of FBXO43 in cell cycle progression and growth of cancer cells. Specifically, FBXO43 acts as a positive cell cycle regulator with an oncogenic activity in variety types of human cancer, including non-small cell lung cancer, hepatocellular carcinoma and sarcoma. Mechanistically, FBXO43 interacts with phosphorylated SKP2 induced by AKT1, leading to reduced SKP2 auto-ubiquitylation and subsequent proteasome degradation. Taken together, our study demonstrates that FBXO43 promotes cell cycle progression by stabilizing SKP2, and FBXO43 could serve as a potential anti-cancer target.
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