• 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

苯并(a)芘的十二种异构酚的皮肤肿瘤起始活性。

Skin tumor-initiating activities of the twelve isomeric phenols of benzo(a)pyrene.

作者信息

Slaga T J, Bracken W M, Dresner S, Levin W, Yagi H, Jerina D M, Conney A H

出版信息

Cancer Res. 1978 Mar;38(3):678-81.

PMID:626971
Abstract

The skin tumor-initiating activities of the 12 isomeric phenols of benzo(a)pyrene (BP) were determined in mice by use of a two-stage system of tumorigenesis. 11-Hydroxybenzo(a)pyrene was moderately active, whereas 2-hydroxybenzo(a)pyrene and BP were strong tumor initiators when applied topically to CD-1 mice and followed by twice-weekly applications of the promoter 12-O-tetradecanoylphorbol-13-acetate. 1-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, and 12-hydroxybenzo(a)pyrene had less than 5% of the tumor-initiating activity of BP when the data were expressed as papillomas per mouse. After 30 weeks of promotion, the number of papillomas per mouse was 8.4, 8.5, and 2.8, respectively, for the animals treated with BP, 2-hydroxybenzo(a)pyrene, and 11-hydroxybenzo(a)pyrene. A 5-week latency period before the appearance of the first tumor was observed after the application of either 2-hydroxybenzo(a)pyrene or BP, whereas a slightly longer latency period of 7 weeks was observed following application of 11-hydroxybenzo(a)pyrene. The time required for 50% of the animals to develop tumors was 13 weeks for animals treated with BP and 15 weeks for animals treated with 2- or 11-hydroxybenzo(a)pyrene.

摘要

利用肿瘤发生的两阶段系统,在小鼠中测定了苯并(a)芘(BP)的12种异构体酚类的皮肤肿瘤起始活性。当局部应用于CD-1小鼠,随后每周两次应用启动子12-O-十四酰佛波醇-13-乙酸酯时,11-羟基苯并(a)芘具有中等活性,而2-羟基苯并(a)芘和BP是强肿瘤起始剂。当数据表示为每只小鼠的乳头状瘤时,1-、3-、4-、5-、6-、7-、8-、9-、10-和12-羟基苯并(a)芘的肿瘤起始活性低于BP的5%。在促进30周后,用BP、2-羟基苯并(a)芘和11-羟基苯并(a)芘处理的动物每只小鼠的乳头状瘤数量分别为8.4、8.5和2.8。在应用2-羟基苯并(a)芘或BP后,观察到在第一个肿瘤出现前有5周的潜伏期,而在应用11-羟基苯并(a)芘后观察到稍长的7周潜伏期。用BP处理的动物50%发生肿瘤所需的时间为13周,用2-或11-羟基苯并(a)芘处理的动物为15周。

相似文献

1
Skin tumor-initiating activities of the twelve isomeric phenols of benzo(a)pyrene.苯并(a)芘的十二种异构酚的皮肤肿瘤起始活性。
Cancer Res. 1978 Mar;38(3):678-81.
2
Tumorigenic activity of benzo(e)pyrene derivatives on mouse skin and in newborn mice.苯并(e)芘衍生物对小鼠皮肤及新生小鼠的致癌活性。
Cancer Res. 1980 Feb;40(2):203-6.
3
Comparison of the tumor-initiating activities of benzo(a)pyrene arene oxides and diol-epoxides.苯并(a)芘芳烃氧化物和二醇环氧化物的肿瘤起始活性比较。
Cancer Res. 1977 Nov;37(11):4130-3.
4
Comparative tumor-initiating activity of methylated benzo(a)pyrene derivatives in mouse skin.甲基化苯并(a)芘衍生物在小鼠皮肤中的肿瘤起始活性比较
Cancer Res. 1980 Apr;40(4):1073-6.
5
Marked differences in the tumor-initiating activity of optically pure (+)- and (-)-trans-7,8-dihydroxy-7,8-dihydrobenzo(a)pyrene on mouse skin.光学纯的(+)-和(-)-反式-7,8-二羟基-7,8-二氢苯并(a)芘对小鼠皮肤的肿瘤起始活性存在显著差异。
Cancer Res. 1977 Aug;37(8 Pt 1):2721-5.
6
Lack of involvement of 6-hydroxymethylation in benzo[a]pyrene skin tumor initiation in mice.6-羟甲基化在小鼠苯并[a]芘诱发皮肤肿瘤起始过程中未发挥作用。
J Natl Cancer Inst. 1978 Aug;61(2):451-5.
7
Lack of carcinogenicity of 4-, 5-, 6-, 7-, 8-, 9-, and 10-hydroxybenzo(a)pyrene on mouse skin.
Cancer Res. 1976 Oct;36(10):3625-8.
8
Metabolism and tumorigenicity of 7-, 8-, 9-, and 10-fluorobenzo(a)pyrenes.7-、8-、9-和10-氟苯并(a)芘的代谢与致瘤性
Cancer Res. 1982 Nov;42(11):4779-83.
9
NTP Initiation/Promotion Study of o-Benzyl-p-Chlorophenol (CAS No. 120-32-1) in Swiss (CD-1(R)) Mice (Mouse Skin Study).邻苄基对氯苯酚(CAS编号:120 - 32 - 1)在瑞士(CD - 1(R))小鼠中的NTP启动/促进研究(小鼠皮肤研究)
Natl Toxicol Program Tech Rep Ser. 1995 May;444:1-136.
10
Carcinogenicity of 2-hydroxybenzo(a)pyrene and 6-hydroxybenzo(a)pyrene in newborn mice.2-羟基苯并(a)芘和6-羟基苯并(a)芘对新生小鼠的致癌性。
Cancer Res. 1979 Jul;39(7 Pt 1):2660-4.

引用本文的文献

1
Enhanced aggressiveness of benzopyrene-induced squamous carcinomas in transgenic mice overexpressing the proprotein convertase PACE4 (PCSK6).在过表达前体蛋白转化酶PACE4(PCSK6)的转基因小鼠中,苯并芘诱导的鳞状细胞癌侵袭性增强。
Mol Carcinog. 2015 Oct;54(10):1122-31. doi: 10.1002/mc.22183. Epub 2014 May 21.
2
Tumor-initiating activity in mouse skin and carcinogenicity in rat mammary gland of fluorinated derivatives of benzo[a]pyrene and 3-methylcholanthrene.苯并[a]芘和3-甲基胆蒽的氟化衍生物在小鼠皮肤中的肿瘤起始活性及在大鼠乳腺中的致癌性。
J Cancer Res Clin Oncol. 1988;114(1):16-22. doi: 10.1007/BF00390480.
3
SENCAR mouse skin tumorigenesis model versus other strains and stocks of mice.
SENCAR小鼠皮肤肿瘤发生模型与其他品系和种群的小鼠对比
Environ Health Perspect. 1986 Sep;68:27-32. doi: 10.1289/ehp.866827.