Molecular Mechanisms of Radiation-Induced Cancer Cell Death: A Primer
Open accessAbstract
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, TP53 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 hematopoietic 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 trialed. 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, focusing on their molecular mechanisms, factors affecting their initiation, and their implications on immunogenicity.
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Not just cell intrinsic factors are involved in radiation-induced cell death, but also the microenvironment, including immunogenic cell death enhanced by radiation.
“It is also increasingly appreciated that not just cell intrinsic factors are involved, but also the microenvironment, including immunogenic cell death enhanced by radiation ( 19 ).”
From Normal-Tissue Tolerance to Radiopharmaceutical Therapies, the Knowns and the Unknowns (2021) · cites this paper as [19]
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References 103 · Cited by 378
- Authors
- Sia, J., Szmyd, R., Hau, E., & Gee, H. E.
- Affiliations
- The University of Melbourne (AU)
- The University of Sydney (AU)
- Corresponding author
- Gee, Harriet E.
- Venue
- Frontiers in Cell and Developmental Biology
- Publisher
- Frontiers Media SA
- Published
- 2020-02-13
- Volume
- 8
- Pages
- 41-41
- ISSN
- 2296-634X (ISSN-L)
- PMC
- PMC7031160
- OpenAlex
- W3005837382
- Cited by
- 378
- References
- 103
- Citations by year
- 2026: 32 · 2025: 55 · 2024: 65 · 2023: 68 · 2022: 77 · 2021: 62 · 2020: 18
- FWCI
- 5.38
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Cell and Developmental Biology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Minerva Access (University of Melbourne) (submittedVersion, cc-by)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Effects of Radiation Exposure
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Radiation Therapy and Dosimetry
- Keywords
- radiation-induced cell death, radiotherapy, mitotic catastrophe, stereotactic body radiotherapy, radiosensitizers, DNA repair, TP53, cell cycle, tumor microenvironment, immunogenicity, treatment resistance, hematologic malignancies, solid tumors
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