Wang Wei, Nag Subhasree, Zhang Xu, Wang Ming-Hai, Wang Hui, Zhou Jianwei, Zhang Ruiwen
Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, Texas, 79106; Cancer Biology Center, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, Texas, 79106.
Med Res Rev. 2015 Mar;35(2):225-85. doi: 10.1002/med.21327. Epub 2014 Aug 28.
Ribosomes are essential components of the protein synthesis machinery. The process of ribosome biogenesis is well organized and tightly regulated. Recent studies have shown that ribosomal proteins (RPs) have extraribosomal functions that are involved in cell proliferation, differentiation, apoptosis, DNA repair, and other cellular processes. The dysfunction of RPs has been linked to the development and progression of hematological, metabolic, and cardiovascular diseases and cancer. Perturbation of ribosome biogenesis results in ribosomal stress, which triggers activation of the p53 signaling pathway through RPs-MDM2 interactions, resulting in p53-dependent cell cycle arrest and apoptosis. RPs also regulate cellular functions through p53-independent mechanisms. We herein review the recent advances in several forefronts of RP research, including the understanding of their biological features and roles in regulating cellular functions, maintaining cell homeostasis, and their involvement in the pathogenesis of human diseases. We also highlight the translational potential of this research for the identification of molecular biomarkers, and in the discovery and development of novel treatments for human diseases.
核糖体是蛋白质合成机制的重要组成部分。核糖体生物发生过程组织有序且受到严格调控。最近的研究表明,核糖体蛋白(RPs)具有核糖体之外的功能,参与细胞增殖、分化、凋亡、DNA修复及其他细胞过程。RPs功能失调与血液学、代谢、心血管疾病及癌症的发生发展有关。核糖体生物发生的紊乱会导致核糖体应激,通过RPs-MDM2相互作用触发p53信号通路的激活,从而导致p53依赖的细胞周期停滞和凋亡。RPs还通过不依赖p53的机制调节细胞功能。我们在此综述了RP研究几个前沿领域的最新进展,包括对其生物学特性以及在调节细胞功能、维持细胞稳态和参与人类疾病发病机制方面作用的理解。我们还强调了该研究在鉴定分子生物标志物以及发现和开发人类疾病新疗法方面的转化潜力。