Zaher Amira, Duchman Bryce, Ivanovic Marina, Spitz Douglas R, Furqan Muhammad, Allen Bryan G, Petronek Michael S
Department of Radiation Oncology, Division of Free Radical and Radiation Biology, University of Iowa, Iowa City, IA 52242, USA.
Division of Pulmonary, Critical Care, Sleep Medicine & Physiology, UC San Diego Health, San Diego, CA 92093, USA.
Bioengineering (Basel). 2024 Feb 14;11(2):182. doi: 10.3390/bioengineering11020182.
Radiation therapy (RT) is an integral and commonly used therapeutic modality for primary lung cancer. However, radiation-induced lung injury (RILI) limits the irradiation dose used in the lung and is a significant source of morbidity. Disruptions in iron metabolism have been linked to radiation injury, but the underlying mechanisms remain unclear.
To utilize a targeted radiation delivery approach to induce RILI for the development of a model system to study the role of radiation-induced iron accumulation in RILI.
This study utilizes a Small Animal Radiation Research Platform (SARRP) to target the right lung with a 20 Gy dose while minimizing the dose delivered to the left lung and adjacent heart. Long-term pulmonary function was performed using RespiRate-x64image analysis. Normal-appearing lung volumes were calculated using a cone beam CT (CBCT) image thresholding approach in 3D Slicer software. Quantification of iron accumulation was performed spectrophotometrically using a ferrozine-based assay as well as histologically using Prussian blue and via Western blotting for ferritin heavy chain expression.
Mild fibrosis was seen histologically in the irradiated lung using hematoxylin and eosin-stained fixed tissue at 9 months, as well as using a scoring system from CBCT images, the Szapiel scoring system, and the highest fibrotic area metric. In contrast, no changes in breathing rate were observed, and median survival was not achieved up to 36 weeks following irradiation, consistent with mild lung fibrosis when only one lung was targeted. Our study provided preliminary evidence on increased iron content and ferritin heavy chain expression in the irradiated lung, thus warranting further investigation.
A targeted lung irradiation model may be a useful approach for studying the long-term pathological effects associated with iron accumulation and RILI following ionizing radiation.
放射治疗(RT)是原发性肺癌不可或缺且常用的治疗方式。然而,放射性肺损伤(RILI)限制了肺部放疗剂量,并且是发病的重要原因。铁代谢紊乱与放射损伤有关,但其潜在机制仍不清楚。
利用靶向放射递送方法诱导RILI,以建立一个模型系统来研究放射诱导的铁积累在RILI中的作用。
本研究利用小动物放射研究平台(SARRP)对右肺进行20 Gy剂量的靶向照射时,尽量减少对左肺和相邻心脏的照射剂量。使用RespiRate-x64图像分析进行长期肺功能检测。在3D Slicer软件中,采用锥束CT(CBCT)图像阈值法计算外观正常的肺体积。使用基于亚铁嗪的测定法通过分光光度法对铁积累进行定量,以及使用普鲁士蓝进行组织学定量,并通过蛋白质印迹法检测铁蛋白重链表达。
在9个月时,使用苏木精和伊红染色的固定组织对受照射的肺进行组织学观察,以及使用CBCT图像评分系统、Szapiel评分系统和最大纤维化面积指标,均可见轻度纤维化。相比之下,未观察到呼吸频率变化,并且在照射后36周内未达到中位生存期,这与仅对一侧肺进行靶向照射时出现的轻度肺纤维化一致。我们的研究提供了初步证据,表明受照射肺中铁含量和铁蛋白重链表达增加,因此值得进一步研究。
靶向肺照射模型可能是研究电离辐射后与铁积累和RILI相关的长期病理效应的有用方法。