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Balancing neurotrophin pathway and sortilin function: Its role in human disease

  • Canterbury Christ Church University
  • Liverpool University Dental Hospital
  • University of Liverpool

Research output: Contribution to journalReview articlepeer-review

Abstract

Neurotensin receptor-3 or sortilin is a vacuolar protein sorting 10 protein domain (Vps10p) has been firstly discovered in the human brain, it acts as receptor or co-receptor of the cell and traffics different proteins within the cell. Sortilin deregulation contributes to the development of several diseases, including neurological diseases and cancer. On the other hand, neurotrophins which are a family of proteins essential for the nervous system development, function and plasticity. The first discovered member is the nerve growth factor; other members are brain-derived growth factor, neurotrophin-3 and neurotrophin-4. Nerve growth factor and brain-derived growth factor are the common neurotrophins that have a role in cancer. Neurotrophins initiate their signals through interaction with tyrosine receptor kinases TrkA, TrkB, and TrkC; each member has an affinity for a specific receptor to stimulate cell survival, while the interaction with p75NTR initiates cell apoptosis pathway by forming a complex with sortilin and neurotrophin precursors. A number of therapeutic approaches are emerging to target the neurotrophins pathway as well as sortilin.

Original languageEnglish
Pages (from-to)188429
JournalBiochimica et Biophysica Acta - Reviews on Cancer
Volume1874
Issue number2
DOIs
Publication statusPublished - 1 Dec 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adaptor Proteins, Vesicular Transport/metabolism
  • Gene Expression Regulation
  • Humans
  • Neoplasms/metabolism
  • Nerve Growth Factors/metabolism
  • Nervous System Diseases/metabolism
  • Protein Transport
  • Receptor Protein-Tyrosine Kinases/metabolism
  • Signal Transduction

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