• 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

Correlation of initiating potency of skin carcinogens with potency to induce resistance to terminal differentiation in cultured mouse keratinocytes.

作者信息

Kilkenny A E, Morgan D, Spangler E F, Yuspa S H

出版信息

Cancer Res. 1985 May;45(5):2219-25.

PMID:3921239
Abstract

The induction by chemical carcinogens of resistance to terminal differentiation in cultured mouse keratinocytes has been proposed to represent a cellular change associated with the initiation phase of skin carcinogenesis. Previous results with this culture model indicated that the number of differentiation-resistant foci was correlated with the dose and known potency for several chemical carcinogens. Assay conditions were optimized to provide quantitative results for screening a variety of carcinogens for their potency as inducers of foci resistant to terminal differentiation. Eight skin initiators of varying potency and from different chemical classes and ultraviolet light were studied for their activity to induce this alteration in cultured epidermal cells from newborn BALB/c mice. There was an excellent positive correlation for the potency of these agents as initiators in vivo and as inducers of altered differentiation in vitro. The induction of resistant foci was independent of the relative cytotoxic effects of each agent except where cytotoxicity was extensive and reduced the number of foci. The results support the hypothesis that initiation of carcinogenesis in skin results in an alteration in the program of epidermal cell differentiation. The results also suggest that the assay is useful for identifying relative potency classes (strong, moderate, weak) of initiating agents.

摘要

相似文献

1
Correlation of initiating potency of skin carcinogens with potency to induce resistance to terminal differentiation in cultured mouse keratinocytes.
Cancer Res. 1985 May;45(5):2219-25.
2
Initiator and promoter induced specific changes in epidermal function and biological potential.引发剂和促癌剂可引起表皮功能和生物学潜能的特定变化。
J Supramol Struct Cell Biochem. 1981;17(3):245-57. doi: 10.1002/jsscb.380170306.
3
Benzo(a)pyrene-DNA adduct formation and removal in mouse epidermis in vivo and in vitro: relationship of DNA binding to initiation of skin carcinogenesis.苯并(a)芘-DNA加合物在小鼠表皮中的体内外形成与去除:DNA结合与皮肤癌发生起始的关系
Cancer Res. 1984 Sep;44(9):4087-95.
4
Adult gerbil epidermal cells resistant to terminal differentiation associated with initiation of carcinogenesis.成年沙鼠表皮细胞对与致癌作用起始相关的终末分化具有抗性。
Acta Cient Venez. 1997;48(3):134-8.
5
Association of resistance to terminal differentiation with initiation of carcinogenesis in adult mouse epidermal cells.
Cancer Res. 1985 Jun;45(6):2748-52.
6
Molecular and cellular basis for tumor promotion in mouse skin.小鼠皮肤肿瘤促进的分子和细胞基础。
Princess Takamatsu Symp. 1983;14:315-26.
7
Mechanisms of initiation and promotion in mouse epidermis.小鼠表皮起始和促癌的机制。
IARC Sci Publ. 1984(56):191-204.
8
Enhanced skin carcinogenesis in cyclin D1-conditional transgenic mice: cyclin D1 alters keratinocyte response to calcium-induced terminal differentiation.细胞周期蛋白D1条件性转基因小鼠皮肤癌发生增强:细胞周期蛋白D1改变角质形成细胞对钙诱导的终末分化的反应。
Cancer Res. 2002 Mar 15;62(6):1641-7.
9
Connexin expression in epidermal cell lines from SENCAR mouse skin tumors.SENCAR小鼠皮肤肿瘤表皮细胞系中的连接蛋白表达。
Mol Carcinog. 1996 Mar;15(3):190-201. doi: 10.1002/(SICI)1098-2744(199603)15:3<190::AID-MC5>3.0.CO;2-M.
10
A course of very small doses of DMBA, each of them allegedly with no promoting potency, acts with clear synergistic effect as a strong promoter of DMBA-initiated mouse skin carcinogenesis. A comparison of the tumorigenic and carcinogenic effects of DMBA (7,12-dimethylbenz-alpha-anthracene) and TPA (12-O-tetradecanoyl-phorbol-13-acetate) used as initiators and promoters in classical two-stage experimental protocols.一系列非常小剂量的二甲基苯并蒽(DMBA),据称每剂都没有促癌能力,但作为DMBA引发的小鼠皮肤癌发生的强力促进剂却具有明显的协同作用。比较了在经典的两阶段实验方案中用作引发剂和促进剂的二甲基苯并蒽(7,12 - 二甲基苯并-α-蒽,DMBA)和十四酰佛波醇乙酯(TPA)的致瘤和致癌作用。
APMIS Suppl. 1994;41:1-38.

引用本文的文献

1
Isolation and short-term culture of primary keratinocytes, hair follicle populations and dermal cells from newborn mice and keratinocytes from adult mice for in vitro analysis and for grafting to immunodeficient mice.从新生小鼠中分离并短期培养原代角质形成细胞、毛囊细胞群和真皮细胞,以及从成年小鼠中分离角质形成细胞,用于体外分析和移植到免疫缺陷小鼠体内。
Nat Protoc. 2008;3(5):799-810. doi: 10.1038/nprot.2008.50.
2
Transgenic mice and squamous multistage skin carcinogenesis.转基因小鼠与鳞状多阶段皮肤癌发生
Cancer Metastasis Rev. 1995 Jun;14(2):113-24. doi: 10.1007/BF00665795.
3
c-myc and c-fos expression in differentiating mouse primary keratinocytes.
c-myc和c-fos在分化的小鼠原代角质形成细胞中的表达。
EMBO J. 1986 Nov;5(11):2853-7. doi: 10.1002/j.1460-2075.1986.tb04579.x.
4
Transfection of the EJ rasHa gene into keratinocytes derived from carcinogen-induced mouse papillomas causes malignant progression.将EJ rasHa基因转染到由致癌物诱导的小鼠乳头瘤衍生的角质形成细胞中会导致恶性进展。
Mol Cell Biol. 1986 Sep;6(9):3144-9. doi: 10.1128/mcb.6.9.3144-3149.1986.
5
The malignant conversion step of mouse skin carcinogenesis.小鼠皮肤癌发生的恶性转化步骤。
Environ Health Perspect. 1990 Aug;88:193-5. doi: 10.1289/ehp.9088193.