Ribosomal protein L6 suppresses hepatocellular carcinoma by modulating FBXO22-mediated p53 degradation

IF 3.7 2区 生物学 Q2 CELL BIOLOGY Cellular signalling Pub Date : 2025-03-01 Epub Date: 2025-01-21 DOI:10.1016/j.cellsig.2025.111612
Zhen Lei , Yiming Luo , Qinggang Fu , Junli Lu , Chao Wang , Long Zhang , Zhiwei Zhang
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Abstract

The ribosomal protein L6 (RPL6) is significant in the progression of different cancer types. However, its precise role in hepatocellular carcinoma (HCC) remains unclear. This research demonstrated that the expression levels of RPL6 are notably decreased in HCC tissues. The decreased expression of RPL6 is strongly linked to tumor size, the presence of vascular invasion, and a worse prognosis. Functional experiments revealed that the expression of RPL6 impedes the proliferation of HCC cells and the advancement of xenograft tumors. Mechanistically, we found that RPL6 binds to and is degraded by the E3 ubiquitin ligase FBXO22, thereby inhibiting the polyubiquitination and subsequent degradation of p53 by FBXO22. The enhanced activity of p53 further contributes to cell growth inhibition. In contrast, the levels of p53 decreased significantly following RPL6 depletion, indicating that RPL6 is essential for the stabilization of p53. In summary, RPL6 inhibits the proliferation of HCC cells via the FBXO22/p53 signaling pathway, suggesting its potential as a biomarker and a therapeutic target for HCC.
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核糖体蛋白L6通过调节fbxo22介导的p53降解抑制肝细胞癌。
核糖体蛋白L6 (RPL6)在不同癌症类型的进展中具有重要意义。然而,其在肝细胞癌(HCC)中的确切作用尚不清楚。本研究表明,RPL6在HCC组织中的表达水平明显降低。RPL6表达的降低与肿瘤大小、血管浸润和较差的预后密切相关。功能实验显示,RPL6的表达可以抑制肝癌细胞的增殖和异种移植肿瘤的进展。在机制上,我们发现RPL6与E3泛素连接酶FBXO22结合并被其降解,从而抑制了FBXO22对p53的多泛素化和随后的降解。p53活性的增强进一步抑制了细胞的生长。相反,p53水平在RPL6缺失后显著下降,表明RPL6对p53的稳定至关重要。综上所述,RPL6通过FBXO22/p53信号通路抑制HCC细胞的增殖,提示其作为HCC生物标志物和治疗靶点的潜力。
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来源期刊
Cellular signalling
Cellular signalling 生物-细胞生物学
CiteScore
8.40
自引率
0.00%
发文量
250
审稿时长
27 days
期刊介绍: Cellular Signalling publishes original research describing fundamental and clinical findings on the mechanisms, actions and structural components of cellular signalling systems in vitro and in vivo. Cellular Signalling aims at full length research papers defining signalling systems ranging from microorganisms to cells, tissues and higher organisms.
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