Unraveling Mitochondrial Determinants of Tumor Response to Radiation Therapy

被引:7
作者
Zaffaroni, Mattia [1 ]
Vincini, Maria Giulia [1 ]
Corrao, Giulia [1 ]
Marvaso, Giulia [1 ,2 ]
Pepa, Matteo [1 ]
Viglietto, Giuseppe [3 ]
Amodio, Nicola [3 ]
Jereczek-Fossa, Barbara Alicja [1 ,2 ]
机构
[1] IRCCS, Div Radiat Oncol, IEO European Inst Oncol, I-20141 Milan, Italy
[2] Univ Milan, Dept Oncol & Hematooncol, I-20122 Milan, Italy
[3] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, I-88100 Catanzaro, Italy
关键词
mitochondria; radiotherapy; radioresistance; ROS; tumor hypoxia; mitochondria-targeting compounds; INDUCED GENOMIC INSTABILITY; IONIZING-RADIATION; OXIDATIVE STRESS; TARGETING HYPOXIA; RADIOTHERAPY EFFICACY; CANCER; METABOLISM; METFORMIN; RADIORESISTANCE; COMBINATION;
D O I
10.3390/ijms231911343
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Radiotherapy represents a highly targeted and efficient treatment choice in many cancer types, both with curative and palliative intents. Nevertheless, radioresistance, consisting in the adaptive response of the tumor to radiation-induced damage, represents a major clinical problem. A growing body of the literature suggests that mechanisms related to mitochondrial changes and metabolic remodeling might play a major role in radioresistance development. In this work, the main contributors to the acquired cellular radioresistance and their relation with mitochondrial changes in terms of reactive oxygen species, hypoxia, and epigenetic alterations have been discussed. We focused on recent findings pointing to a major role of mitochondria in response to radiotherapy, along with their implication in the mechanisms underlying radioresistance and radiosensitivity, and briefly summarized some of the recently proposed mitochondria-targeting strategies to overcome the radioresistant phenotype in cancer.
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页数:13
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