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- W2924069622 abstract "Collapsin response mediator proteins (CRMPs) are a family of ubiquitously expressed, homologous phosphoproteins best known for coordinating cytoskeletal formation and regulating cellular division, migration, polarity, and synaptic connection. CRMP2, the most studied of the five family members, is best known for its affinity for tubulin heterodimers and function in regulating the microtubule network. These functions are tightly regulated by post-translational modifications including phosphorylation, SUMOylation, oxidation, and O-GlcNAcylation. While CRMP2’s physiological functions rely mostly on its non-phosphorylated state, dysregulation of CRMP2 phosphorylation and SUMOylation has been reported to be involved in the pathophysiology of multiple diseases including cancer, chronic pain, spinal cord injury, neurofibromatosis type 1, and others. Here, we provide a consolidated update on what is known about CRMP2 signaling and function, first focusing on axonal growth and neuronal polarity, then illustrating the link between dysregulated CRMP2 post-translational modifications and diseases. We additionally discuss the roles of CRMP2 in non-neuronal cells, both in the CNS and regions of the periphery. Finally, we offer thoughts on the therapeutic implications of modulating CRMP2 function in a variety of diseases." @default.
- W2924069622 created "2019-04-01" @default.
- W2924069622 creator A5007835784 @default.
- W2924069622 creator A5012031138 @default.
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- W2924069622 creator A5045111286 @default.
- W2924069622 creator A5078663344 @default.
- W2924069622 creator A5079797658 @default.
- W2924069622 date "2019-03-27" @default.
- W2924069622 modified "2023-10-15" @default.
- W2924069622 title "Dysregulation of CRMP2 Post-Translational Modifications Drive Its Pathological Functions" @default.
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