» Articles » PMID: 32117972

Molecular Mechanisms of Radiation-Induced Cancer Cell Death: A Primer

Overview
Specialty Cell Biology
Date 2020 Mar 3
PMID 32117972
Citations 149
Authors
Affiliations
Soon will be listed here.
Abstract

Radiation therapy (RT) is responsible for at least 40% of cancer cures, however treatment resistance remains a clinical problem. There have been recent advances in understanding the molecular mechanisms of radiation-induced cell death. The type of cell death after radiation depends on a number of factors including cell type, radiation dose and quality, oxygen tension, status, DNA repair capacity, cell cycle phase at time of radiation exposure, and the microenvironment. Mitotic catastrophe (a pathway preceding cell death that happens in mitosis or as a consequence of aberrant mitotic progression) is the primary context of radiation-induced cell death in solid cancers, although in a small subset of cancers such as haematopoietic malignancies, radiation results in immediate interphase apoptosis, occurring within hours after exposure. There is intense therapeutic interest in using stereotactic ablative body radiotherapy (SABR), a precise, high-dose form of RT given in a small number of fractions, to prime the immune system for cancer cell killing, but the optimal radiation dose and fractionation remain unclear. Additionally, promising novel radiosensitisers targeting the cell cycle and DNA repair pathways are being trialled. In the context of the increasing use of SABR and such novel agents in the clinic, we provide an updated primer on the major types of radiation-induced cell death, focussing on their molecular mechanisms, factors affecting their initiation, and their implications on immunogenicity.

Citing Articles

Enhancing radiation-induced reactive oxygen species generation through mitochondrial transplantation in human glioblastoma.

Marshall K, Velayutham M, Khramtsov V, Mizener A, Cifarelli C Sci Rep. 2025; 15(1):7618.

PMID: 40038364 PMC: 11880374. DOI: 10.1038/s41598-025-91331-2.


A VAT1-related gene signature predicts radioresistance in gliomas.

Shan X, Sun Z, Huang R, Wang K, Qiu X, Yang P Heliyon. 2025; 11(4):e42583.

PMID: 40034328 PMC: 11875813. DOI: 10.1016/j.heliyon.2025.e42583.


Unravelling physical and radiobiological effects of proton boron fusion reaction with anionic metallacarboranes ([o-COSAN]) in breast cancer cells.

Belchior A, Alves B, Mendes E, Megre F, Alves L, Santos P EJNMMI Res. 2025; 15(1):13.

PMID: 39982528 PMC: 11845649. DOI: 10.1186/s13550-025-01199-6.


Biophysics at the edge of life and death: radical control of apoptotic mechanisms.

Hack S, Beane W, Tseng K Front Cell Death. 2025; 2.

PMID: 39897412 PMC: 11784940. DOI: 10.3389/fceld.2023.1147605.


The role of cGAS-STING pathway in the development of radiation-induced lung injury.

Zhao X, Du L, Ma N, Tan X, Lei X, Zhang P J Cancer Res Clin Oncol. 2025; 151(2):48.

PMID: 39856464 PMC: 11761121. DOI: 10.1007/s00432-025-06088-y.


References
1.
Brown J, Brenner D, Carlson D . Dose escalation, not "new biology," can account for the efficacy of stereotactic body radiation therapy with non-small cell lung cancer. Int J Radiat Oncol Biol Phys. 2013; 85(5):1159-60. PMC: 3608927. DOI: 10.1016/j.ijrobp.2012.11.003. View

2.
Vakkila J, Lotze M . Inflammation and necrosis promote tumour growth. Nat Rev Immunol. 2004; 4(8):641-8. DOI: 10.1038/nri1415. View

3.
Dikic I, Elazar Z . Mechanism and medical implications of mammalian autophagy. Nat Rev Mol Cell Biol. 2018; 19(6):349-364. DOI: 10.1038/s41580-018-0003-4. View

4.
Kroemer G, Galluzzi L, Vandenabeele P, Abrams J, Alnemri E, Baehrecke E . Classification of cell death: recommendations of the Nomenclature Committee on Cell Death 2009. Cell Death Differ. 2008; 16(1):3-11. PMC: 2744427. DOI: 10.1038/cdd.2008.150. View

5.
Grassberger C, Ellsworth S, Wilks M, Keane F, Loeffler J . Assessing the interactions between radiotherapy and antitumour immunity. Nat Rev Clin Oncol. 2019; 16(12):729-745. DOI: 10.1038/s41571-019-0238-9. View