TNFRSF13B gene mutation in familial acute myeloid leukemia : A new piece in the complex scenario of hereditary predisposition?

© 2023 The Authors. Hematological Oncology published by John Wiley & Sons Ltd..

TNFRSF13B mutations are widely associated with common variable immunodeficiency. TNFRSF13B was recently counted among relevant genes associated with childhood-onset of hematological malignancies; nonetheless, its role in acute myeloid leukemia (AML) remains unexplored. We report the study of a family with two cases of AML, sharing a germline TNFRSF13B mutation favoring the formation of a more stable complex with its ligand TNFSF13: a positive regulator of AML-initiating cells. Our data turn the spotlight onto the TNFRSF13B role in AML onset, inserting a new fragment into the complex scenario of a hereditary predisposition to myeloid neoplasms.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:41

Enthalten in:

Hematological oncology - 41(2023), 5 vom: 21. Dez., Seite 942-946

Sprache:

Englisch

Beteiligte Personen:

Cumbo, Cosimo [VerfasserIn]
Orsini, Paola [VerfasserIn]
Tarantini, Francesco [VerfasserIn]
Anelli, Luisa [VerfasserIn]
Zagaria, Antonella [VerfasserIn]
Tragni, Vincenzo [VerfasserIn]
Coccaro, Nicoletta [VerfasserIn]
Tota, Giuseppina [VerfasserIn]
Parciante, Elisa [VerfasserIn]
Conserva, Maria Rosa [VerfasserIn]
Redavid, Immacolata [VerfasserIn]
Minervini, Crescenzio Francesco [VerfasserIn]
Minervini, Angela [VerfasserIn]
Attolico, Immacolata [VerfasserIn]
Gentile, Mattia [VerfasserIn]
Pierri, Ciro Leonardo [VerfasserIn]
Specchia, Giorgina [VerfasserIn]
Musto, Pellegrino [VerfasserIn]
Albano, Francesco [VerfasserIn]

Links:

Volltext

Themen:

Case Reports
Familial AML
Hereditary predisposition
TNFRSF13B
TNFRSF13B protein, human
Transmembrane Activator and CAML Interactor Protein

Anmerkungen:

Date Completed 16.12.2023

Date Revised 16.12.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1002/hon.3212

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM360343783