• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

2 MeV 快中子诱导 Ptch1+/- 小鼠髓母细胞瘤的高相对生物学效应,该小鼠在染色体 13 上具有辐射特异性缺失。

High Relative Biological Effectiveness of 2 MeV Fast Neutrons for Induction of Medulloblastoma in Ptch1+/- Mice with Radiation-specific Deletion on Chromosome 13.

机构信息

Department of Radiation Effects Research, National Institute of Radiological Sciences, National Institutes for Quantum and Radiological Science and Technology, Chiba, Japan.

Institute for Environmental Science, Kamikita-gun, Aomori, Japan.

出版信息

Radiat Res. 2021 Aug 1;196(2):225-234. doi: 10.1667/RADE-20-00025.1.

DOI:10.1667/RADE-20-00025.1
PMID:34046685
Abstract

Neutron radiation, a high-linear energy transfer radiation, has a high relative biological effectiveness (RBE) for various end points. The age at exposure is an important modifier of the effects of radiation, including carcinogenesis, with infants being generally more radiosensitive. Ptch1+/- mice offer a unique experimental system for assessing radiation carcinogenesis. Spontaneous development of medulloblastoma tumors occurs in nonirradiated animals that lose their Ptch1+ allele, most frequently by a loss of heterozygosity (LOH) of chromosome 13 via recombination or non-disjunction (referred to as S-type tumors). In contrast, tumors occur in irradiated Ptch1+/- mice as a result of chromosome 13 LOH with an interstitial deletion (R-type), making spontaneous and radiation-induced tumors discernible. To elucidate the influence of age on the effect of fast neutrons, we irradiated Ptch1+/- mice with neutrons (mean energy, ∼2 MeV) or γ rays on embryonic day (E)14 and E17 and on postnatal day (P)1, 4 or 10 and classified the resulting medulloblastomas based on chromosome 13 aberrations. Instead of LOH, some tumors harbored mutations in their Ptch1+ gene via a nonirradiation-associated mechanism such as duplication, insertion, base substitution or deletion with microhomology-mediated end joining; thus, these tumors were classified as S-type. The RBE regarding the induction of R-type tumors was 12.9 (8.6, 17.2), 9.6 (6.9, 12.3), 21.5 (17.2, 25.8), and 7.1 (4.7, 9.5) (mean and 95% confidence interval) for mice irradiated on E14, E17, P1 and P4, respectively, with the highest value seen during the most active development of the tissue and P10 being completely resistant. These results indicate that the developmental stage at exposure of the tissue influences the RBE of neutrons.

摘要

中子辐射是一种高线性能量转移辐射,对各种终点具有高相对生物效应(RBE)。暴露年龄是辐射效应的重要调节剂,包括致癌作用,婴儿通常更敏感。Ptch1+/- 小鼠为评估辐射致癌作用提供了一个独特的实验系统。非照射动物中自发发生髓母细胞瘤肿瘤,这些动物失去了 Ptch1+等位基因,最常见的是通过染色体 13 的重组或非分离(称为 S 型肿瘤)丢失杂合性(LOH)。相比之下,在照射的 Ptch1+/- 小鼠中,由于染色体 13 的 LOH 伴有中间缺失(R 型)而发生肿瘤,从而可区分自发和辐射诱导的肿瘤。为了阐明年龄对快中子效应的影响,我们在胚胎期(E)14 日和 17 日以及出生后(P)1、4 或 10 日用中子(平均能量,约 2 MeV)或γ射线照射 Ptch1+/- 小鼠,并根据染色体 13 异常对所得的髓母细胞瘤进行分类。一些肿瘤通过非照射相关机制(如复制、插入、碱基替换或缺失伴微同源介导的末端连接)在其 Ptch1+基因中产生突变,而不是 LOH;因此,这些肿瘤被归类为 S 型。诱导 R 型肿瘤的 RBE 分别为 12.9(8.6,17.2)、9.6(6.9,12.3)、21.5(17.2,25.8)和 7.1(4.7,9.5)(平均值和 95%置信区间)对于分别在 E14、E17、P1 和 P4 照射的小鼠,最高值出现在组织最活跃发育期间,而 P10 完全抵抗。这些结果表明,组织暴露的发育阶段影响中子的 RBE。

相似文献

1
High Relative Biological Effectiveness of 2 MeV Fast Neutrons for Induction of Medulloblastoma in Ptch1+/- Mice with Radiation-specific Deletion on Chromosome 13.2 MeV 快中子诱导 Ptch1+/- 小鼠髓母细胞瘤的高相对生物学效应,该小鼠在染色体 13 上具有辐射特异性缺失。
Radiat Res. 2021 Aug 1;196(2):225-234. doi: 10.1667/RADE-20-00025.1.
2
Relative Biological Effectiveness of Carbon Ion Beams for Induction of Medulloblastoma with Radiation-specific Chromosome 13 Deletion in Ptch1+/- Mice.碳离子射线诱导 Ptch1+/- 小鼠髓母细胞瘤及其辐射特异性 13 号染色体缺失的相对生物效应。
Radiat Res. 2024 Sep 1;202(3):503-509. doi: 10.1667/RADE-23-00229.1.
3
Sensitive Detection of Radiation-Induced Medulloblastomas after Acute or Protracted Gamma-Ray Exposures in Ptch1 Heterozygous Mice Using a Radiation-Specific Molecular Signature.利用辐射特异性分子特征对Ptch1杂合小鼠急性或长期γ射线照射后辐射诱导的髓母细胞瘤进行灵敏检测。
Radiat Res. 2016 Oct;186(4):407-414. doi: 10.1667/RR14499.1. Epub 2016 Sep 30.
4
Genomic and gene expression signatures of radiation in medulloblastomas after low-dose irradiation in Ptch1 heterozygous mice.在 Ptch1 杂合子小鼠中低剂量照射后髓母细胞瘤中的辐射的基因组和基因表达特征。
Carcinogenesis. 2010 Sep;31(9):1694-701. doi: 10.1093/carcin/bgq145. Epub 2010 Jul 8.
5
Transgenerational inheritance of enhanced susceptibility to radiation-induced medulloblastoma in newborn Ptch1⁺/⁻ mice after paternal irradiation.父系照射后新生Ptch1⁺/⁻小鼠对辐射诱导的髓母细胞瘤易感性增强的跨代遗传。
Oncotarget. 2015 Nov 3;6(34):36098-112. doi: 10.18632/oncotarget.5553.
6
Cancer risk from low dose radiation in Ptch1 mice with inactive DNA repair systems: Therapeutic implications for medulloblastoma.Ptch1 小鼠中低剂量辐射的致癌风险:对髓母细胞瘤的治疗意义。
DNA Repair (Amst). 2019 Feb;74:70-79. doi: 10.1016/j.dnarep.2018.12.003. Epub 2018 Dec 16.
7
Influence of Age on Leukemia Mortality Associated with Exposure to γ rays and 2-MeV Fast Neutrons in Male C3H Mice.年龄对雄性 C3H 小鼠接受 γ 射线和 2-MeV 快中子照射所致白血病死亡率的影响。
Radiat Res. 2024 Oct 1;202(4):685-696. doi: 10.1667/RADE-23-00069.1.
8
Lung-Cancer Risk in Mice after Exposure to Gamma Rays, Carbon Ions or Neutrons: Egfr Pathway Activation and Frequent Nuclear Abnormality.暴露于伽马射线、碳离子或中子后的小鼠肺癌风险:表皮生长因子受体(Egfr)通路激活与频繁的核异常
Radiat Res. 2022 Nov 1;198(5):475-487. doi: 10.1667/RADE-21-00192.1.
9
Survival and diseases in C57BL mice exposed to X rays or 3.1 MeV neutrons at an age of 7 or 21 days.7日龄或21日龄的C57BL小鼠在接受X射线或3.1兆电子伏特中子照射后的存活情况及疾病发生情况。
Radiat Res. 1996 Oct;146(4):453-60.
10
Age Modifies the Effect of 2-MeV Fast Neutrons on Rat Mammary Carcinogenesis.年龄改变2兆电子伏快中子对大鼠乳腺癌发生的影响。
Radiat Res. 2017 Oct;188(4):419-425. doi: 10.1667/RR14829.1. Epub 2017 Aug 15.

引用本文的文献

1
Trans-Scale Insights into Variability in Radiation Cancer Risk Across Tissues, Individuals, and Species.跨尺度洞察组织、个体和物种间辐射致癌风险的变异性
Biology (Basel). 2025 Aug 9;14(8):1025. doi: 10.3390/biology14081025.
2
Establishment and activity of the planning and acting network for low dose radiation research in Japan (PLANET): 2016-2023.日本低剂量辐射研究计划与行动网络(PLANET)的建立与活动:2016-2023 年。
J Radiat Res. 2024 Sep 24;65(5):561-574. doi: 10.1093/jrr/rrae049.
3
Newly discovered genomic mutation patterns in radiation-induced small intestinal tumors of ApcMin/+ mice.
新发现的 ApcMin/+ 小鼠辐射诱导小肠肿瘤中的基因组突变模式。
PLoS One. 2023 Oct 12;18(10):e0292643. doi: 10.1371/journal.pone.0292643. eCollection 2023.
4
Interstitial deletion of the Apc locus in β-catenin-overexpressing cells is a signature of radiation-induced intestinal tumors in C3B6F1 ApcMin/+ mice†.β-连环蛋白过表达细胞中 APC 基因座的间质缺失是 C3B6F1 ApcMin/+ 小鼠辐射诱导肠道肿瘤的特征。
J Radiat Res. 2023 May 25;64(3):622-631. doi: 10.1093/jrr/rrad021.
5
Inhibitory Effect of Ursolic Acid on Proliferation and Migration of Renal Carcinoma Cells and Its Mechanism.乌索酸对肾癌细胞增殖和迁移的抑制作用及其机制。
Comput Intell Neurosci. 2022 May 4;2022:1529132. doi: 10.1155/2022/1529132. eCollection 2022.