TY - JOUR
T1 - Deregulation of New Cell Death Mechanisms in Leukemia
AU - Favale, Gregorio
AU - Donnarumma, Federica
AU - Capone, Vincenza
AU - Della Torre, Laura
AU - Beato, Antonio
AU - Carannante, Daniela
AU - Verrilli, Giulia
AU - Nawaz, Asmat
AU - Grimaldi, Francesco
AU - De Simone, Maria Carla
AU - Del Gaudio, Nunzio
AU - Megchelenbrink, Wouter Leonard
AU - Caraglia, Michele
AU - Benedetti, Rosaria
AU - Altucci, Lucia
AU - Carafa, Vincenzo
N1 - Publisher Copyright:
© 2024 by the authors.
PY - 2024/5
Y1 - 2024/5
N2 - 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.
AB - 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.
KW - drug discovery
KW - drug resistance
KW - drug-induced cell death
KW - leukemia
KW - regulated cell death
UR - https://www.scopus.com/pages/publications/85192774008
U2 - 10.3390/cancers16091657
DO - 10.3390/cancers16091657
M3 - Review article
AN - SCOPUS:85192774008
SN - 2072-6694
VL - 16
JO - Cancers
JF - Cancers
IS - 9
M1 - 1657
ER -