• 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

一种用于研究大鼠肝脏致癌作用起始和促进过程的新方案及其理论依据。

A new protocol and its rationale for the study of initiation and promotion of carcinogenesis in rat liver.

作者信息

Potter V R

出版信息

Carcinogenesis. 1981;2(12):1375-9. doi: 10.1093/carcin/2.12.1375.

DOI:10.1093/carcin/2.12.1375
PMID:7326837
Abstract

A new protocol for carcinogenesis in rat liver is described in order that confirmatory experiments might be undertaken concurrently. The basic protocol, designated IPI (initiator + promoter + initiator), is presented in several alternative forms including the possible use of X-irradiation as the initiator. The rationale is discussed in terms of the two-hit somatic mutation theory of Armitage and Doll, with an initial hit produced by the first dose of initiator and expansion of single cells to sizable clones by promotion thereby increasing the probability of a second hit by the second dose of initiator. The question of relevant mutations is taken up and it is proposed that genes for chalones and for chalone receptors are logical targets for consideration in a two-mutation sequence.

摘要

本文描述了一种新的大鼠肝癌发生实验方案,以便能同时进行验证性实验。基本方案被命名为IPI(启动剂+促进剂+启动剂),有几种不同形式,包括可能使用X射线作为启动剂。依据阿米蒂奇和多尔的双打击体细胞突变理论对该原理进行了讨论,首次剂量的启动剂产生初始打击,促进剂使单个细胞扩增为相当大的克隆,从而增加了第二次剂量启动剂产生第二次打击的可能性。文中讨论了相关突变的问题,并提出抑素和抑素受体的基因是双突变序列中值得考虑的合理靶点。

相似文献

1
A new protocol and its rationale for the study of initiation and promotion of carcinogenesis in rat liver.一种用于研究大鼠肝脏致癌作用起始和促进过程的新方案及其理论依据。
Carcinogenesis. 1981;2(12):1375-9. doi: 10.1093/carcin/2.12.1375.
2
Alternative hypotheses for the role of promotion in chemical carcinogenesis.关于促进作用在化学致癌过程中所起作用的其他假说。
Environ Health Perspect. 1983 Apr;50:139-48. doi: 10.1289/ehp.8350139.
3
Effect of lithocholic acid on DL-ethionine carcinogenesis in rat liver.石胆酸对大鼠肝脏中DL-乙硫氨酸致癌作用的影响。
Gan. 1971 Aug;62(4):239-45.
4
Synergism in carcinogenesis.致癌作用中的协同作用。
Food Cosmet Toxicol. 1968 Dec;6(4):520-3.
5
[Synergism between orally active carcinogens. IV. Results of simultaneous feeding of 4 carcinogens in rats].[口服活性致癌物之间的协同作用。IV. 大鼠同时投喂4种致癌物的结果]
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1967;257(1):12.
6
Dose-response characteristics of aflatoxin B1 carcinogenesis in the rat.黄曲霉毒素B1在大鼠体内致癌作用的剂量-反应特征。
Cancer Res. 1967 Dec;27(12):2370-6.
7
Promotion of hepatocarcinogenesis in humans and animal models.人类和动物模型中肝癌发生的促进作用。
Arch Toxicol. 2008 Sep;82(9):623-31. doi: 10.1007/s00204-007-0273-7. Epub 2008 Jan 16.
8
[Experimental investigations in "syncarcinogenesis". VI. Addition of minimum doses of 4 different liver carcinogens in rats in liver cancer development].
Z Krebsforsch. 1970;74(4):457-66.
9
Short-term in vivo initiation/promotion bioassay for hepatocarcinogens.
J Environ Pathol Toxicol. 1980 Nov;4(5-6):39-46.
10
Some conclusions derived from a liver model for carcinogenesis.从一个肝脏致癌模型得出的一些结论。
Natl Cancer Inst Monogr. 1981 Dec(58):49-53.

引用本文的文献

1
Inorganic arsenic trioxide induces gap junction loss in association with the downregulation of connexin43 and E-cadherin in rat hepatic "stem-like" cells.三氧化二砷诱导大鼠肝“干细胞样”细胞缝隙连接丢失,与连接蛋白 43 和 E-钙黏蛋白下调有关。
Kaohsiung J Med Sci. 2014 Feb;30(2):57-67. doi: 10.1016/j.kjms.2013.10.002. Epub 2013 Dec 8.
2
Inhibition of gap junctional Intercellular communication in WB-F344 rat liver epithelial cells by triphenyltin chloride through MAPK and PI3-kinase pathways.三苯基锡通过 MAPK 和 PI3-激酶通路抑制 WB-F344 大鼠肝上皮细胞缝隙连接细胞间通讯。
J Occup Med Toxicol. 2010 Jun 30;5:17. doi: 10.1186/1745-6673-5-17.
3
Mechanisms of multistep carcinogenesis and carcinogen risk assessment.
多步骤致癌作用机制与致癌物风险评估
Environ Health Perspect. 1993 Apr;100:9-20. doi: 10.1289/ehp.931009.
4
Genetic alterations in thyroid tumor progression: association with p53 gene mutations.甲状腺肿瘤进展中的基因改变:与p53基因突变的关联
Jpn J Cancer Res. 1993 May;84(5):526-31. doi: 10.1111/j.1349-7006.1993.tb00171.x.
5
Hepatic proliferation inhibitor.肝增殖抑制剂。
Mol Cell Biochem. 1984;59(1-2):57-80. doi: 10.1007/BF00231305.
6
Alternative hypotheses for the role of promotion in chemical carcinogenesis.关于促进作用在化学致癌过程中所起作用的其他假说。
Environ Health Perspect. 1983 Apr;50:139-48. doi: 10.1289/ehp.8350139.
7
Cellular and molecular mechanisms of multistep carcinogenesis: relevance to carcinogen risk assessment.多步骤致癌作用的细胞和分子机制:与致癌物风险评估的相关性。
Environ Health Perspect. 1987 Dec;76:65-70. doi: 10.1289/ehp.877665.
8
Progressive dysplasia and aneuploidy are hallmarks of mouse skin papillomas: relevance to malignancy.进行性发育异常和非整倍体是小鼠皮肤乳头瘤的标志:与恶性肿瘤的相关性。
Proc Natl Acad Sci U S A. 1987 Apr;84(7):2029-32. doi: 10.1073/pnas.84.7.2029.
9
Progression: the terminal stage in carcinogenesis.进展:致癌作用的终末阶段。
Jpn J Cancer Res. 1989 Jul;80(7):599-607. doi: 10.1111/j.1349-7006.1989.tb01683.x.
10
Biological bases for cancer dose-response extrapolation procedures.癌症剂量反应外推程序的生物学基础。
Environ Health Perspect. 1991 Jan;90:293-6. doi: 10.1289/ehp.90-1519475.