Abstract
External beam radiation therapy (RT) is a cornerstone of modern cancer management, being utilized in both curative and palliative settings due to its safety, efficacy, and widespread availability. A primary biological effect of RT is DNA damage, which leads to significant cytostatic and cytotoxic effects. Importantly, malignant cells possess a limited capacity for DNA repair compared to normal cells, and when combined with irradiation techniques that minimize damage to healthy tissues, this creates an advantageous therapeutic window. However, the clinical effectiveness of RT also appears to involve both direct and indirect interactions between RT and non-transformed components of the tumoral ecosystem, particularly immune cells. In this review, we describe the molecular and cellular mechanisms by which irradiated cancer cells modify the immunological tumor microenvironment and how such changes ultimately impact tumor growth.
| Original language | English |
|---|---|
| Pages (from-to) | 678-693 |
| Number of pages | 16 |
| Journal | Cell Chemical Biology |
| Volume | 32 |
| Issue number | 5 |
| Early online date | Apr 22 2025 |
| DOIs | |
| State | Published - May 15 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- CD8 cytotoxic T lymphocytes
- CGAS/STING signaling
- PD-1
- dendritic cells
- immune checkpoint inhibitors
- tumor-associated macrophages
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