AraC interacts with p75


Journal

Cell death & disease
ISSN: 2041-4889
Titre abrégé: Cell Death Dis
Pays: England
ID NLM: 101524092

Informations de publication

Date de publication:
17 07 2023
Historique:
received: 22 04 2023
accepted: 11 07 2023
revised: 29 06 2023
medline: 19 7 2023
pubmed: 18 7 2023
entrez: 17 7 2023
Statut: epublish

Résumé

Cytosine arabinoside (AraC) is one of the main therapeutic treatments for several types of cancer, including acute myeloid leukaemia. However, after a high-dose AraC chemotherapy regime, patients develop severe neurotoxicity and cell death in the central nervous system leading to cerebellar ataxia, dysarthria, nystagmus, somnolence and drowsiness. AraC induces apoptosis in dividing cells. However, the mechanism by which it leads to neurite degeneration and cell death in mature neurons remains unclear. We hypothesise that the upregulation of the death receptor p75

Identifiants

pubmed: 37460457
doi: 10.1038/s41419-023-05979-7
pii: 10.1038/s41419-023-05979-7
pmc: PMC10352303
doi:

Substances chimiques

Receptor, Nerve Growth Factor 0
Receptors, Nerve Growth Factor 0
Ngfr protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

440

Informations de copyright

© 2023. The Author(s).

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Auteurs

Vanessa Lopes-Rodrigues (V)

Department of Physiology and Life Sciences Institute, National University of Singapore, Singapore, 117597, Singapore.

Pia Boxy (P)

Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark.

Eunice Sim (E)

Department of Physiology and Life Sciences Institute, National University of Singapore, Singapore, 117597, Singapore.

Dong Ik Park (DI)

Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark.

Michael Habeck (M)

Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark.
Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.

Josep Carbonell (J)

Department of Neuroscience, Karolinska Institute, Stockholm, S-17177, Sweden.

Annika Andersson (A)

Department of Neuroscience, Karolinska Institute, Stockholm, S-17177, Sweden.

Diana Fernández-Suárez (D)

Department of Neuroscience, Karolinska Institute, Stockholm, S-17177, Sweden.

Poul Nissen (P)

Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark.
Department of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.

Anders Nykjær (A)

Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark.

Lilian Kisiswa (L)

Department of Biomedicine, Aarhus University, Aarhus, Denmark. liki@biomed.au.dk.
Danish Research Institute of Translational Neuroscience (DANDRITE)-Nordic EMBL Partnership for Molecular Medicine, Aarhus University, Aarhus, Denmark. liki@biomed.au.dk.
The Danish National Research Foundation Center, PROMEMO, Aarhus University, Aarhus, Denmark. liki@biomed.au.dk.

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