Edmondson E F, Gatti D M, Ray F A, Garcia E L, Fallgren C M, Kamstock D A, Weil M M
Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Colorado State University, Fort Collins, CO 80523, USA.
Sci Adv. 2020 Apr 15;6(16):eaax5940. doi: 10.1126/sciadv.aax5940. eCollection 2020 Apr.
Cancer risk from galactic cosmic radiation exposure is considered a potential "showstopper" for a manned mission to Mars. Calculating the actual risks confronted by spaceflight crews is complicated by our limited understanding of the carcinogenic effects of high-charge, high-energy (HZE) ions, a radiation type for which no human exposure data exist. Using a mouse model of genetic diversity, we find that the histotype spectrum of HZE ion-induced tumors is similar to the spectra of spontaneous and γ-ray-induced tumors and that the genomic loci controlling susceptibilities overlap between groups for some tumor types. Where it occurs, this overlap indicates shared tumorigenesis mechanisms regardless of the type of radiation exposure and supports the use of human epidemiological data from γ-ray exposures to predict cancer risks from galactic cosmic rays.
来自银河宇宙辐射暴露的癌症风险被认为是载人火星任务的一个潜在“阻碍因素”。由于我们对高电荷、高能(HZE)离子的致癌作用了解有限,计算航天机组人员面临的实际风险变得复杂,对于这种辐射类型,不存在人类暴露数据。利用遗传多样性的小鼠模型,我们发现HZE离子诱导肿瘤的组织型谱与自发和γ射线诱导肿瘤的谱相似,并且对于某些肿瘤类型,控制易感性的基因组位点在各组之间重叠。这种重叠出现的地方表明,无论辐射暴露类型如何,肿瘤发生机制都是相同的,并支持使用来自γ射线暴露的人类流行病学数据来预测银河宇宙射线导致的癌症风险。