• 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

正常及化学诱导增生性表皮中暗细胞数量随动物年龄及肿瘤促进剂效率的变化

Numerical variation of dark cells in normal and chemically induced hyperplastic epidermis with age of animal and efficiency of tumor promoter.

作者信息

Klein-Szanto A J, Slaga T J

出版信息

Cancer Res. 1981 Nov;41(11 Pt 1):4437-40.

PMID:6796260
Abstract

The percentages of dark keratinocytes was quantitatively assessed in normal epidermis of Sencar mice before and after birth and in adult epidermis after topical application of several compounds of varying promoting efficiency. The percentage of dark keratinocytes reached a maximum at the 19th day of gestation (approximately 40%) and fell abruptly after birth (approximately 3%). Old animals exhibited a very low number of dark basal cells (0.2%). After topical application of the weak promoters resiniferotoxin, anthralin, ethylphenylpropiolate, and 12-deoxyphorbol-13-2,4,6-decatrienoate, the percentage of dark cells in young adult epidermis did not differ markedly from that in control (acetone-treated) specimens. The strong first-stage promoters 4-O-methyl-12-O-tetradecanoylphorbol-13-acetate and calcium ionophore A 23187, as well as the strong complete promoter 12-deoxyphorbol-13-deoxyphorbol-13-decanoate, induced the appearance of large numbers of dark keratinocytes, in a percentage similar to that seen after 12-O-tetradecanoylphorbol-13-acetate application (approximately 20%). The similarities between the dark keratinocytes seen after topical application of 12-O-tetradecanoylphorbol-13-acetate or other strong promoters and the dark cells observed in the fetal epidermis before the onset of the adult type of epidermal keratinization indicate that potent and/or first stage tumor promoters can be identified by their ability to induce cells resembling fetal-type dedifferentiated keratinocytes.

摘要

在出生前后的Sencar小鼠正常表皮以及成年表皮局部应用几种具有不同促进效率的化合物后,对深色角质形成细胞的百分比进行了定量评估。深色角质形成细胞的百分比在妊娠第19天达到最高(约40%),出生后急剧下降(约3%)。老年动物的深色基底细胞数量非常少(0.2%)。在局部应用弱启动子树脂毒素、蒽林、乙基苯基丙炔酸酯和12-脱氧佛波醇-13-2,4,6-癸三烯酸酯后,年轻成年表皮中深色细胞的百分比与对照(丙酮处理)标本相比无明显差异。强的第一阶段启动子4-O-甲基-12-O-十四烷酰佛波醇-13-乙酸酯和钙离子载体A 23187,以及强的完全启动子12-脱氧佛波醇-13-脱氧佛波醇-13-癸酸酯,诱导出现大量深色角质形成细胞,其百分比与应用12-O-十四烷酰佛波醇-13-乙酸酯后所见相似(约20%)。局部应用12-O-十四烷酰佛波醇-13-乙酸酯或其他强启动子后所见的深色角质形成细胞与成年型表皮角质化开始前胎儿表皮中观察到的深色细胞之间的相似性表明,强效和/或第一阶段肿瘤启动子可以通过其诱导类似于胎儿型去分化角质形成细胞的细胞的能力来识别。

相似文献

1
Numerical variation of dark cells in normal and chemically induced hyperplastic epidermis with age of animal and efficiency of tumor promoter.正常及化学诱导增生性表皮中暗细胞数量随动物年龄及肿瘤促进剂效率的变化
Cancer Res. 1981 Nov;41(11 Pt 1):4437-40.
2
Quantitative evaluation of dark keratinocytes induced by several promoting and hyperplasiogenic agents: their use as an early morphological indicator of tumor-promoting action.几种促癌和增生剂诱导的暗角质形成细胞的定量评估:其作为肿瘤促进作用早期形态学指标的应用。
Carcinog Compr Surv. 1982;7:305-9.
3
Cutaneous changes during prolonged application of 12-O-tetradecanoylphorbol-13-acetate on mouse skin and residual effects after cessation of treatment.12 - O - 十四酰佛波醇 - 13 - 乙酸酯长期涂抹于小鼠皮肤期间的皮肤变化及停药后的残留效应。
Cancer Res. 1985 Jun;45(6):2753-9.
4
Activation of the epidermal growth factor receptor by skin tumor promoters and in skin tumors from SENCAR mice.皮肤肿瘤启动子及SENCAR小鼠皮肤肿瘤中表皮生长因子受体的激活
Cell Growth Differ. 1995 Nov;6(11):1447-55.
5
Activation of erbB2 and c-src in phorbol ester-treated mouse epidermis: possible role in mouse skin tumor promotion.佛波酯处理的小鼠表皮中erbB2和c-src的激活:在小鼠皮肤肿瘤促进中的可能作用。
Oncogene. 1997 Mar 27;14(12):1435-44. doi: 10.1038/sj.onc.1200980.
6
Induction of dark keratinocytes by 12-O-tetradecanoylphorbol-13-acetate and mezerein as an indicator of tumor-promoting efficiency.以12-O-十四烷酰佛波醇-13-乙酸酯和芫花酯甲诱导暗角质形成细胞作为肿瘤促进效率的指标。
Carcinogenesis. 1980 May;1(5):399-406. doi: 10.1093/carcin/1.5.399.
7
A morphometric study of dedifferentiated and involutional dark keratinocytes in 12-O-tetradecanoylphorbol-13-acetate-treated mouse epidermis.12-O-十四酰佛波醇-13-乙酸酯处理的小鼠表皮中去分化和退化深色角质形成细胞的形态计量学研究。
Cancer Res. 1984 Jun;44(6):2711-7.
8
Host factors in the susceptibility of mice to tumour initiating and promoting agents.小鼠对肿瘤引发剂和促进剂易感性中的宿主因素。
IARC Sci Publ. 1983(51):257-73.
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
Effects of single applications of 12-O-tetradecanoylphorbol-13-acetate, mezerein, or ethylphenylpropiolate on DNA synthesis and polyamine levels in hairless mouse epidermis.单次应用12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯、大戟二萜醇酯或苯丙炔酸乙酯对无毛小鼠表皮DNA合成和多胺水平的影响。
Cancer Res. 1983 Sep;43(9):4126-31.

引用本文的文献

1
Overview of tumor promotion in animals.动物肿瘤促进作用概述。
Environ Health Perspect. 1983 Apr;50:3-14. doi: 10.1289/ehp.83503.
2
Effects of chronic topical application of 12-O-tetradecanoylphorbol-13-acetate on the skin and internal organs of SENCAR mice.长期局部应用12-O-十四酰佛波醇-13-乙酸酯对SENCAR小鼠皮肤和内脏器官的影响。
Environ Health Perspect. 1986 Sep;68:75-80. doi: 10.1289/ehp.866875.
3
Epidermal tissue homeostasis: apoptosis and cell emigration as mechanisms of controlled cell deletion in the epidermis of the toad, Bufo bufo.
表皮组织稳态:凋亡和细胞迁移作为蟾蜍(Bufo bufo)表皮中受控细胞清除的机制。
Cell Tissue Res. 1989 Jun;256(3):475-86. doi: 10.1007/BF00225595.