TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study.
Journal
NPJ precision oncology
ISSN: 2397-768X
Titre abrégé: NPJ Precis Oncol
Pays: England
ID NLM: 101708166
Informations de publication
Date de publication:
14 Jul 2021
14 Jul 2021
Historique:
received:
08
10
2020
accepted:
16
04
2021
entrez:
15
7
2021
pubmed:
16
7
2021
medline:
16
7
2021
Statut:
epublish
Résumé
In children with cancer, the heterogeneity in ototoxicity occurrence after similar treatment suggests a role for genetic susceptibility. Using a genome-wide association study (GWAS) approach, we identified a genetic variant in TCERG1L (rs893507) to be associated with hearing loss in 390 non-cranial irradiated, cisplatin-treated children with cancer. These results were replicated in two independent, similarly treated cohorts (n = 192 and 188, respectively) (combined cohort: P = 5.3 × 10
Identifiants
pubmed: 34262104
doi: 10.1038/s41698-021-00178-z
pii: 10.1038/s41698-021-00178-z
pmc: PMC8280110
doi:
Types de publication
Journal Article
Langues
eng
Pagination
64Investigateurs
A C H de Vries
(ACH)
M van Grotel
(M)
E van Dulmen-den Broeder
(E)
A L F van der Kooi
(ALF)
L C M Kremer
(LCM)
H J H van der Pal
(HJH)
G Calaminus
(G)
A E Hoetink
(AE)
M M van den Heuvel-Eibrink
(MM)
Informations de copyright
© 2021. The Author(s).
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