Typical NF2 and LTZR1 mutations are retained in an immortalized human schwann cell model of schwannomatosis.
Journal
Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560
Informations de publication
Date de publication:
15 Oct 2024
15 Oct 2024
Historique:
received:
19
06
2024
revised:
26
09
2024
accepted:
03
10
2024
medline:
24
10
2024
pubmed:
24
10
2024
entrez:
24
10
2024
Statut:
epublish
Résumé
Human SCs play a primary role in SWN, a rare genetic disorder in which patients develop multiple schwannomas. So that, their isolation and immortalization could represent an irreplaceable tool to investigate the disease etiopathology. Although few clones of tumoural SCs have been obtained, unfortunately they present genetic, morphological and biological characteristics that do not fully represent the original cells. Herein we isolated, characterized and immortalized primary SCs from human schwannomas. Our immortalized human SCs present typical
Identifiants
pubmed: 39444403
doi: 10.1016/j.heliyon.2024.e38957
pii: S2405-8440(24)14988-2
pmc: PMC11497399
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e38957Informations de copyright
© 2024 The Authors. Published by Elsevier Ltd.
Déclaration de conflit d'intérêts
The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Valerio Magnaghi reports financial support was provided by the Ministry of University and Research (MUR). Other authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.