Department of Radiation Oncology, Duke University School of Medicine, Durham, North Carolina.
Department of Radiation Oncology, Baylor College of Medicine, Houston, Texas.
Radiat Res. 2024 Nov 1;202(5):734-744. doi: 10.1667/RADE-24-00004.1.
The main deterrent to long-term space travel is the risk of Radiation Exposure Induced Death (REID). The National Aeronautics and Space Administration (NASA) has adopted Permissible Exposure Levels (PELs) to limit the probability of REID to 3% for the risk of death due to radiation-induced carcinogenesis. The most significant contributor to current REID estimates for astronauts is the risk of lung cancer. Recently updated lung cancer estimates from Japan's atomic bomb survivors showed that the excess relative risk of lung cancer by age 70 is roughly fourfold higher in females compared to males. However, whether sex differences may impact the risk of lung cancer due to exposure to high charge and energy (HZE) radiation is not well studied. Thus, to evaluate the impact of sex differences on the risk of solid cancer development after HZE radiation exposure, we irradiated Rbfl/fl, Trp53fl/+ male and female mice infected with Adeno-Cre with various doses of 320 kVp X rays or 600 MeV/n 56Fe ions and monitored them for any radiation-induced malignancies. We conducted complete necropsy and histopathology of major organs on 183 male and 157 female mice after following them for 350 days postirradiation. We observed that lung adenomas/carcinomas and esthesioneuroblastomas (ENBs) were the most common primary malignancies in mice exposed to X rays and 56Fe ions, respectively. In addition, 1 Gy 56Fe-ion exposure compared to X-ray exposure led to a significantly increased incidence of lung adenomas/carcinomas (P = 0.02) and ENBs (P < 0.0001) in mice. However, we did not find a significantly higher incidence of any solid malignancies in female mice as compared to male mice, regardless of radiation quality. Furthermore, gene expression analysis of ENBs suggested a distinct gene expression pattern with similar hallmark pathways altered, such as MYC targets and MTORC1 signaling, in ENBs induced by X rays and 56Fe ions. Thus, our data revealed that 56Fe-ion exposure significantly accelerated the development of lung adenomas/carcinomas and ENBs compared to X rays, but the rate of solid malignancies was similar between male and female mice, regardless of radiation quality.
长期太空旅行的主要障碍是辐射暴露诱发死亡(REID)的风险。美国国家航空航天局(NASA)已采用可接受的暴露水平(PEL),将因辐射诱发致癌而导致 REID 的概率限制在 3%。目前宇航员的 REID 估计中,最大的贡献因素是肺癌风险。最近更新的日本原子弹幸存者的肺癌估计显示,女性到 70 岁时肺癌的超额相对风险比男性高约四倍。然而,性别差异是否会影响因暴露于高电荷和能量(HZE)辐射而导致肺癌的风险尚未得到充分研究。因此,为了评估性别差异对 HZE 辐射暴露后实体癌发展风险的影响,我们用各种剂量的 320 kVp X 射线或 600 MeV/n56Fe 离子照射感染了 Adeno-Cre 的 Rbfl/fl、Trp53fl/+雄性和雌性小鼠,并监测它们是否发生任何辐射诱发的恶性肿瘤。我们对 183 只雄性和 157 只雌性小鼠进行了 350 天的辐射后,对它们进行了完整的尸检和主要器官的组织病理学检查。我们观察到,暴露于 X 射线和 56Fe 离子的小鼠中,肺腺瘤/癌和嗅神经母细胞瘤(ENB)是最常见的原发性恶性肿瘤。此外,与 X 射线照射相比,1 Gy 56Fe 离子照射导致小鼠肺腺瘤/癌(P = 0.02)和 ENB(P < 0.0001)的发生率显著增加。然而,无论辐射质量如何,我们都没有发现雌性小鼠的任何实体恶性肿瘤发生率明显高于雄性小鼠。此外,ENB 的基因表达分析表明,X 射线和 56Fe 离子诱导的 ENB 具有相似的特征途径改变的独特基因表达模式,如 MYC 靶标和 MTORC1 信号。因此,我们的数据表明,与 X 射线相比,56Fe 离子照射显著加速了肺腺瘤/癌和 ENB 的发展,但无论辐射质量如何,雄性和雌性小鼠的实体恶性肿瘤发生率相似。