Acute Myeloid Leukemia (AML) is an aggressive hematological malignancy that relies on highly heterogeneous cytogenetic alterations. Although in the last few years new agents have been developed for AML treatment, the overall survival prospects for AML patients are still gloomy and new therapeutic options are still urgently needed. Constitutive NF-kappa B activation has been reported in around 40% of AML patients, where it sustains AML cell survival and chemoresistance. Given the central role of NF-kappa B in AML, targeting the NF-kappa B pathway represents an attractive strategy to treat AML. This review focuses on current knowledge of NF-kappa B's roles in AML pathogenesis and summarizes the main therapeutic approaches used to treat NF-kappa B-driven AML.

NF-κB: A Druggable Target in Acute Myeloid Leukemia

Di Francesco, Barbara;Verzella, Daniela
;
Capece, Daria;Vecchiotti, Davide;Di Vito Nolfi, Mauro;Flati, Irene;Cornice, Jessica;Di Padova, Monica;Angelucci, Adriano;Alesse, Edoardo;Zazzeroni, Francesca
2022-01-01

Abstract

Acute Myeloid Leukemia (AML) is an aggressive hematological malignancy that relies on highly heterogeneous cytogenetic alterations. Although in the last few years new agents have been developed for AML treatment, the overall survival prospects for AML patients are still gloomy and new therapeutic options are still urgently needed. Constitutive NF-kappa B activation has been reported in around 40% of AML patients, where it sustains AML cell survival and chemoresistance. Given the central role of NF-kappa B in AML, targeting the NF-kappa B pathway represents an attractive strategy to treat AML. This review focuses on current knowledge of NF-kappa B's roles in AML pathogenesis and summarizes the main therapeutic approaches used to treat NF-kappa B-driven AML.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/195417
Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 16
  • ???jsp.display-item.citation.isi??? 14
social impact