• 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

Change in ascorbate radical production in an irradiated experimental tumor with increased tumor size.

作者信息

Isoda H, Akagi K, Murata T, Aoki Y, Ikeda S, Tanaka Y, Kihara T, Ikeda M

机构信息

Department of Radiology, Kansai Medical University, Osaka, Japan.

出版信息

Cancer Res. 1996 Dec 15;56(24):5741-4.

PMID:8971185
Abstract

We have reported that ascorbate radical (Asc.-) could serve as an indicator of the amount of hydroxyl radical and superoxide produced by irradiation in vivo. Using this method, we investigated the relationship between tumor size and Asc.- production after irradiation (10 Gy) and between tumor size and the radical-scavenging ability of WR-2721 (300 mg/kg). Asc.- was measured in normal muscle and SCC-VII tumors transplanted into mice (n = 6). In tumors, the increase in Asc.- significantly decreased with increasing tumor size (r = -0.483; P < 0.05). The increase in Asc.- production after irradiation was more inhibited by WR-2721 in normal muscle tissue than in tumor tissue at various sizes. In tumors, the increase in Asc.- was less inhibited by WR-2721 with increasing tumor size. These results demonstrate that the increase in radical production after irradiation and drug distribution decreased with increasing tumor size and that WR-2721 has excellent differential protection. This method is expected to measure changes in the amounts of local hydroxyl radical and superoxide modified by a change of tumor environment or drug administration.

摘要

相似文献

1
Change in ascorbate radical production in an irradiated experimental tumor with increased tumor size.
Cancer Res. 1996 Dec 15;56(24):5741-4.
2
Detection of an ascorbate radical in an irradiated mice using electron spin resonance (ESR).利用电子自旋共振(ESR)检测辐照小鼠体内的抗坏血酸自由基。
Indian J Exp Biol. 1996 Sep;34(9):898-900.
3
[Measurement of radical in irradiated experimental tumor: direct detection of ascorbate radical in mice using ESR].
Nihon Igaku Hoshasen Gakkai Zasshi. 1995 Sep;55(11):769-73.
4
Detection of an increase in ascorbate radical in an irradiated experimental tumour system using ESR.
Int J Radiat Biol. 1995 Oct;68(4):467-73. doi: 10.1080/09553009514551431.
5
Toxicity, radiation sensitivity modification, and combined drug effects of ascorbic acid with misonidazole in vivo on FSaII murine fibrosarcomas.抗坏血酸与米索硝唑在体内对FSaII小鼠纤维肉瘤的毒性、辐射敏感性改变及联合药物效应
J Natl Cancer Inst. 1987 Aug;79(2):377-81.
6
Comparison of the protective effects of three phosphorothioate radioprotectors in the RIF-1 tumor.三种硫代磷酸酯辐射防护剂对RIF-1肿瘤的保护作用比较。
Radiat Res. 1986 Nov;108(2):167-75.
7
Tissue-protective effects of fullerenol C60(OH)24 and amifostine in irradiated rats.富勒醇C60(OH)24和氨磷汀对辐照大鼠的组织保护作用
Colloids Surf B Biointerfaces. 2007 Jul 1;58(1):39-43. doi: 10.1016/j.colsurfb.2007.01.005. Epub 2007 Jan 16.
8
Ascorbate as a "redox sensor" and protector against irradiation-induced oxidative stress in 32D CL 3 hematopoietic cells and subclones overexpressing human manganese superoxide dismutase.抗坏血酸盐作为“氧化还原传感器”以及对32D CL 3造血细胞和过表达人锰超氧化物歧化酶的亚克隆中辐射诱导的氧化应激的保护剂。
Int J Radiat Oncol Biol Phys. 2004 Mar 1;58(3):851-61. doi: 10.1016/j.ijrobp.2003.10.022.
9
Evaluation of hypoxic cell radio-sensitizers in terms of radio-sensitizing and repair-inhibiting potential. Dependency on p53 status of tumor cells and the effects on intratumor quiescent cells.从放射增敏和修复抑制潜力方面评估乏氧细胞放射增敏剂。取决于肿瘤细胞的p53状态以及对肿瘤内静止细胞的影响。
Anticancer Res. 2006 Mar-Apr;26(2A):1261-70.
10
Modification of radiation induced damage in mouse intestine by WR-2721.WR-2721对小鼠肠道辐射损伤的修饰作用
Indian J Exp Biol. 2000 Jul;38(7):669-74.

引用本文的文献

1
Amifostine alleviates radiation-induced lethal small bowel damage via promotion of 14-3-3σ-mediated nuclear p53 accumulation.氨磷汀通过促进14-3-3σ介导的细胞核p53积累减轻辐射诱导的致死性小肠损伤。
Oncotarget. 2014 Oct 30;5(20):9756-69. doi: 10.18632/oncotarget.2386.