DNA损伤
线性能量转移
DNA修复
放射治疗
质子疗法
粒子疗法
癌症研究
DNA
质子
辐照
化学
免疫系统
生物物理学
离子
医学
生物
生物化学
免疫学
内科学
物理
有机化学
核物理学
量子力学
作者
Gro Elise Rødland,Mihaela Temelie,Adrian Eek Mariampillai,Sissel Hauge,Antoine Gilbert,François Chevalier,Diana Savu,Randi G. Syljuåsen
出处
期刊:Cells
[MDPI AG]
日期:2024-06-19
卷期号:13 (12): 1058-1058
被引量:9
标识
DOI:10.3390/cells13121058
摘要
The use of charged particle radiotherapy is currently increasing, but combination therapy with DNA repair inhibitors remains to be exploited in the clinic. The high-linear energy transfer (LET) radiation delivered by charged particles causes clustered DNA damage, which is particularly effective in destroying cancer cells. Whether the DNA damage response to this type of damage is different from that elicited in response to low-LET radiation, and if and how it can be targeted to increase treatment efficacy, is not fully understood. Although several preclinical studies have reported radiosensitizing effects when proton or carbon ion irradiation is combined with inhibitors of, e.g., PARP, ATR, ATM, or DNA-PKcs, further exploration is required to determine the most effective treatments. Here, we examine what is known about repair pathway choice in response to high- versus low-LET irradiation, and we discuss the effects of inhibitors of these pathways when combined with protons and carbon ions. Additionally, we explore the potential effects of DNA repair inhibitors on antitumor immune signaling upon proton and carbon ion irradiation. Due to the reduced effect on healthy tissue and better immune preservation, particle therapy may be particularly well suited for combination with DNA repair inhibitors.
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