Pang Jiao, Cen Changqian, Tian Yuan, Cao Xingrui, Hao Liang, Tao Xueshu, Cao Zhipeng
Department of Forensic Pathology, School of Forensic Medicine, China Medical University, Shenyang, Liaoning Province, PR China.
Department of Pathology and pathophysiology, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian Province, PR China.
Transl Psychiatry. 2025 Jan 10;15(1):6. doi: 10.1038/s41398-024-03222-1.
The incidence of neurodegenerative diseases (NDs) has increased recently. However, most of the current governance strategies are palliative and lack effective therapeutic drugs. Therefore, elucidating the pathological mechanism of NDs is the key to the development of targeted drugs. As a member of the tyrosine phosphatase family, the role of Shp2 has been studied in tumors, but the research in the nervous system is still in a sporadic state. It can be phosphorylated by tyrosine kinases and then positively regulate tyrosine kinase-dependent signaling pathways. It could also be used as an adaptor protein to mediate downstream signaling pathways. Most of the existing studies have shown that Shp2 may be a potential molecular "checkpoint" against NDs, but its role in promoting degenerative lesions is difficult to ignore as well, and its two-way effect of both activation and inhibition is very distinctive. Shp2 is closely related to NDs-related pathogenic factors such as oxidative stress, mitochondrial dysfunction, excitatory toxicity, immune inflammation, apoptosis, and autophagy. Its bidirectional effects interfere with these pathogenic factors, making it a core component of the feedback and crosstalk network between multiple signaling pathways. Therefore, this article reviews the molecular mechanism of Shp2 regulation in NDs and its regulatory role in various pathogenic factors, providing evidence for the treatment of NDs by targeting Shp2 and the development of molecular targeted drugs.
神经退行性疾病(NDs)的发病率近来有所上升。然而,当前大多数治疗策略都是姑息性的,且缺乏有效的治疗药物。因此,阐明神经退行性疾病的病理机制是开发靶向药物的关键。作为酪氨酸磷酸酶家族的一员,Shp2的作用已在肿瘤研究中有所涉及,但在神经系统中的研究仍处于零散状态。它可被酪氨酸激酶磷酸化,进而正向调节酪氨酸激酶依赖性信号通路。它还可用作衔接蛋白来介导下游信号通路。现有的大多数研究表明,Shp2可能是对抗神经退行性疾病的一个潜在分子“检查点”,但其在促进退行性病变中的作用也不容忽视,其激活和抑制的双向作用非常独特。Shp2与氧化应激、线粒体功能障碍、兴奋性毒性、免疫炎症、细胞凋亡和自噬等神经退行性疾病相关致病因素密切相关。其双向作用干扰这些致病因素,使其成为多条信号通路之间反馈和串扰网络的核心组成部分。因此,本文综述了Shp2在神经退行性疾病中的调控分子机制及其在各种致病因素中的调节作用,为通过靶向Shp2治疗神经退行性疾病及开发分子靶向药物提供依据。