Fudan University Shanghai Cancer Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, 200032, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Cell Death Dis. 2020 Mar 20;11(3):197. doi: 10.1038/s41419-020-2393-4.
The Shwachman-Bodian Diamond syndrome (SBDS)-associated gene, SBDS, is involved in rRNA synthesis and ribosome maturation, but the role of SBDS in cancer is largely elusive. In this study, we found that SBDS is often overexpressed or amplified in human cancers, and high level of endogenous SBDS is significantly associated with unfavorable prognosis. Conversely, knockdown of SBDS leads to p53 stabilization and activation through the ribosomal stress-RPL5/RPL11-MDM2 pathway, resulting in the repression of cancer cell proliferation and invasion. Interestingly, ectopic SBDS in the nucleoplasm also suppresses tumor cell growth and proliferation in vitro and in vivo. Mechanistically, ectopically expressed SBDS triggered by, for example, ribosomal stress binds to the transactivation domain of p53 and perturbs the MDM2-p53 interaction, consequently leading to impaired p53 ubiquitination and proteasomal degradation. Altogether, our finding for the first time demonstrates the dual functions of SBDS in cancer development by coordinating ribosome biogenesis and p53 activity.
Shwachman-Bodian Diamond 综合征(SBDS)相关基因 SBDS 参与 rRNA 合成和核糖体成熟,但 SBDS 在癌症中的作用在很大程度上仍不清楚。在这项研究中,我们发现 SBDS 在人类癌症中经常过表达或扩增,内源性 SBDS 水平高与不良预后显著相关。相反,SBDS 的敲低会通过核糖体应激-RPL5/RPL11-MDM2 途径导致 p53 稳定和激活,从而抑制癌细胞的增殖和侵袭。有趣的是,核质中的异位 SBDS 也能抑制体外和体内肿瘤细胞的生长和增殖。在机制上,例如由核糖体应激触发的异位表达的 SBDS 与 p53 的转录激活结构域结合,并扰乱 MDM2-p53 相互作用,从而导致 p53 泛素化和蛋白酶体降解受损。总之,我们的研究首次表明 SBDS 通过协调核糖体生物发生和 p53 活性在癌症发展中具有双重功能。