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神经系统疾病中Wnt信号过度激活

Excess Wnt in neurological disease.

作者信息

Pascual Danielle M, Jebreili Rizi Delaram, Kaur Harsimran, Marcogliese Paul C

机构信息

Department of Biochemistry and Medical Genetics, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Manitoba, Canada.

Children's Hospital Research Institute of Manitoba (CHRIM), Winnipeg, Manitoba, Canada.

出版信息

Biochem J. 2025 May 16;482(10):601-18. doi: 10.1042/BCJ20240265.

Abstract

Wnt pathways are critical developmental signaling cascades that are conserved across multicellular life. A clear role for Wnt signaling in proper neural development has been well-established, yet less is known about its sustained expression and signaling in the mature nervous system. The precise role for Wnt pathways, canonical or otherwise, and individual Wnt components (ligands, receptors, transducers, effectors, and regulators) in the mature brain are poorly understood. However, genetic evidence implicating Wnt-related components in both neurodevelopmental and neurodegenerative disorders suggests that fine-tuned regulation of Wnt signaling is required for proper nervous system development and long-term homeostasis. Much has been documented about down-regulated Wnt signaling and its association with neurological conditions. Hence, the focus of this review is to consolidate and highlight the evidence for up-regulated Wnt transcription and/or signaling in neurodevelopmental and neurodegenerative disorders with a brief discussion on the role of deregulated Wnt in cancer. Finally, we touch upon the therapeutic prospect of Wnt inhibition in the nervous system.

摘要

Wnt信号通路是多细胞生物中保守的关键发育信号级联反应。Wnt信号在正常神经发育中的明确作用已得到充分证实,但对其在成熟神经系统中的持续表达和信号传导了解较少。Wnt信号通路(经典或其他)以及单个Wnt组分(配体、受体、转导子、效应器和调节剂)在成熟大脑中的精确作用尚不清楚。然而,遗传证据表明Wnt相关组分与神经发育和神经退行性疾病有关,这表明Wnt信号的精细调节对于正常神经系统发育和长期稳态是必需的。关于Wnt信号下调及其与神经系统疾病的关联已有大量文献记载。因此,本综述的重点是巩固和强调神经发育和神经退行性疾病中Wnt转录和/或信号上调的证据,并简要讨论失调的Wnt在癌症中的作用。最后,我们探讨了Wnt抑制在神经系统中的治疗前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcfc/12203940/553b0871de88/BCJ-482-10-BCJ20240265-g001.jpg

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