Yang Zhi-Zhi, Yang Bing, Yan Haiyan, Ma Xingyu, Tian Bin, Zheng Bingqi, Chen Yong-Xian, Dong Yi-Ming, Deng Jinsi, Zhan Ziling, Shi Yanmei, Zhang Jing Yuan, Lu Daning, He Jie-Hua, Zhang Yin, Hu KaiShun, Zhu Shuang, Zhou Keda, Zhang Yu-Chan, Zheng Yiqing, Yin Dong, Liao Jian-You
Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Guangdong-Hong Kong Joint Laboratory for RNA Medicine, Medical Research Center, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, PR China.
Department of Clinical Laboratory, Shenshan Central Hospital, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Shanwei, Guangdong, 516600, PR China.
Nat Commun. 2025 Jan 9;16(1):557. doi: 10.1038/s41467-025-55851-9.
Hyperactivation of ribosome biogenesis (RiBi) drives cancer progression, yet the role of RiBi-associated proteins (RiBPs) in breast cancer (BC) is underexplored. In this study, we perform a comprehensive multi-omics analysis and reveal that assembly and maturation factors (AMFs), a subclass of RiBPs, are upregulated at both RNA and protein levels in BC, correlating with poor patient outcomes. In contrast, ribosomal proteins (RPs) do not show systematic upregulation across various cancers, including BC. We further demonstrate that the oncogenic activation of a top AMF candidate in BC, DCAF13, enhances Pol I transcription and promotes proliferation in BC cells both in vitro and in vivo. Mechanistically, DCAF13 promotes Pol I transcription activity by facilitating the K63-linked ubiquitination of RPA194. This process stimulates global protein synthesis and cell growth. Our findings uncover a modification of RPA194 that regulates Pol I activity; this modification is dysregulated in BC, contributing to cancer progression.
核糖体生物合成(RiBi)的过度激活驱动癌症进展,然而,RiBi相关蛋白(RiBPs)在乳腺癌(BC)中的作用尚未得到充分研究。在本研究中,我们进行了全面的多组学分析,发现作为RiBPs一个亚类的组装和成熟因子(AMFs)在BC的RNA和蛋白质水平上均上调,与患者的不良预后相关。相比之下,核糖体蛋白(RPs)在包括BC在内的各种癌症中并未表现出系统性上调。我们进一步证明,BC中一个顶级AMF候选基因DCAF13的致癌激活增强了Pol I转录,并在体外和体内促进了BC细胞的增殖。从机制上讲,DCAF13通过促进RPA194的K63连接泛素化来促进Pol I转录活性。这一过程刺激了整体蛋白质合成和细胞生长。我们的研究结果揭示了一种调节Pol I活性的RPA194修饰;这种修饰在BC中失调,促进了癌症进展。