Absence of Tissue-Sparing Effects in Partial Proton FLASH Irradiation in Murine Intestine.
Qixian ZhangLeo E GerweckEthan CascioLiqun GuQingyuan YangXinyue DongPeigen HuangAlejandro BertoletKonrad Pawel NesterukWonmo SungAimee L McNamaraSchuemann JanPublished in: Cancers (2023)
Ultra-high dose rate irradiation has been reported to protect normal tissues more than conventional dose rate irradiation. This tissue sparing has been termed the FLASH effect. We investigated the FLASH effect of proton irradiation on the intestine as well as the hypothesis that lymphocyte depletion is a cause of the FLASH effect. A 16 × 12 mm 2 elliptical field with a dose rate of ~120 Gy/s was provided by a 228 MeV proton pencil beam. Partial abdominal irradiation was delivered to C57BL/6j and immunodeficient Rag1 -/- /C57 mice. Proliferating crypt cells were counted at 2 days post exposure, and the thickness of the muscularis externa was measured at 280 days following irradiation. FLASH irradiation did not reduce the morbidity or mortality of conventional irradiation in either strain of mice; in fact, a tendency for worse survival in FLASH-irradiated mice was observed. There were no significant differences in lymphocyte numbers between FLASH and conventional-dose-rate mice. A similar number of proliferating crypt cells and a similar thickness of the muscularis externa following FLASH and conventional dose rate irradiation were observed. Partial abdominal FLASH proton irradiation at 120 Gy/s did not spare normal intestinal tissue, and no difference in lymphocyte depletion was observed. This study suggests that the effect of FLASH irradiation may depend on multiple factors, and in some cases dose rates of over 100 Gy/s do not induce a FLASH effect and can even result in worse outcomes.
Keyphrases
- high dose
- radiation induced
- type diabetes
- optical coherence tomography
- gene expression
- induced apoptosis
- peripheral blood
- cardiovascular disease
- radiation therapy
- cell cycle arrest
- cell proliferation
- low dose
- weight loss
- skeletal muscle
- stem cell transplantation
- signaling pathway
- endoplasmic reticulum stress
- oxidative stress
- robot assisted