Deregulation of New Cell Death Mechanisms in Leukemia

Author:

Favale Gregorio1,Donnarumma Federica1,Capone Vincenza1,Della Torre Laura1,Beato Antonio1,Carannante Daniela1,Verrilli Giulia1,Nawaz Asmat12,Grimaldi Francesco3,De Simone Maria Carla4,Del Gaudio Nunzio1,Megchelenbrink Wouter Leonard15,Caraglia Michele12ORCID,Benedetti Rosaria1ORCID,Altucci Lucia1267ORCID,Carafa Vincenzo12ORCID

Affiliation:

1. Dipartimento di Medicina di Precisione, Università degli Studi della Campania “Luigi Vanvitelli”, 80138 Napoli, Italy

2. Biogem, Molecular Biology and Genetics Research Institute, 83031 Ariano Irpino, Italy

3. Dipartimento di Medicina Clinica e Chirurgia, Divisione di Ematologia, Università degli Studi di Napoli Federico II, 80131 Napoli, Italy

4. A.O.R.N. Cardarelli, Divisione di Ematologia, 80131 Napoli, Italy

5. Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, The Netherlands

6. Institute of Experimental Endocrinology and Oncology “Gaetano Salvatore” (IEOS)-National Research Council (CNR), 80131 Napoli, Italy

7. Programma di Epigenetica Medica, A.O.U. “Luigi Vanvitelli”, 80138 Napoli, Italy

Abstract

Hematological malignancies are among the top five most frequent forms of cancer in developed countries worldwide. Although the new therapeutic approaches have improved the quality and the life expectancy of patients, the high rate of recurrence and drug resistance are the main issues for counteracting blood disorders. Chemotherapy-resistant leukemic clones activate molecular processes for biological survival, preventing the activation of regulated cell death pathways, leading to cancer progression. In the past decade, leukemia research has predominantly centered around modulating the well-established processes of apoptosis (type I cell death) and autophagy (type II cell death). However, the development of therapy resistance and the adaptive nature of leukemic clones have rendered targeting these cell death pathways ineffective. The identification of novel cell death mechanisms, as categorized by the Nomenclature Committee on Cell Death (NCCD), has provided researchers with new tools to overcome survival mechanisms and activate alternative molecular pathways. This review aims to synthesize information on these recently discovered RCD mechanisms in the major types of leukemia, providing researchers with a comprehensive overview of cell death and its modulation.

Funder

MUR-PRIN/PNRR2022

Publisher

MDPI AG

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