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在妊娠第6至20天用7,12 - 二甲基苯并[a]蒽对NMRI小鼠进行经胎盘起始处理,并对F1代小鼠产后用佛波酯12 - O - 十四酰佛波醇 - 13 - 乙酸酯进行处理:皮肤以外器官的肿瘤发生率

Diaplacental initiation of NMRI mice with 7,12-dimethylbenz[a]anthracene during gestation days 6--20 and postnatal treatment of the F1-generation with the phorbol ester 12-O-tetradecanoylphorbol-13-acetate: tumor incidence in organs other than the skin.

作者信息

Goerttler K, Loehrke H, Hesse B, Milz A, Schweizer J

出版信息

Carcinogenesis. 1981;2(11):1087-94. doi: 10.1093/carcin/2.11.1087.

DOI:10.1093/carcin/2.11.1087
PMID:6797749
Abstract

The tumor spectrum and tumor incidence in organs other than the skin were investigated in the 12-O-tetradecanoylphorbol-13-acetate (TPA) treated F 1-generation of 13 groups of NMRI mice which had been initiated by a single intragastric dose of 7,12-dimethylbenz[a]anthracene during days 6, 8, and 10--20 of pregnancy. Promotion by topical application of TPA to the back skin was carried out twice per week 12 weeks after birth over a period of 26 weeks. The forestomach epithelium represented the only organ in which statistically significant 2-stage carcinogenesis could be demonstrated. A promotion effect could be seen in tumors of the Harderian gland, of the liver of male animals and on the development of both benign and malignant tumors of the lung in both sexes. Promotion treatment therefore led to an activation of initiated tumor cells in those organs in which a very sensitive, more or less narrowly spaced oncogenic determination period exists.

摘要

在孕期第6、8和10 - 20天经单次胃内给予7,12 - 二甲基苯并[a]蒽启动的13组NMRI小鼠的F1代中,研究了12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)处理后皮肤以外器官的肿瘤谱和肿瘤发生率。出生后12周开始,每周两次在背部皮肤局部涂抹TPA进行促癌,持续26周。前胃上皮是唯一能证明有统计学意义的两阶段致癌作用的器官。在哈德氏腺肿瘤、雄性动物肝脏肿瘤以及两性肺部良性和恶性肿瘤的发生发展中可观察到促癌作用。因此,促癌治疗导致了那些存在非常敏感、致癌决定期或多或少间隔较窄的器官中已启动的肿瘤细胞的激活。

相似文献

1
Diaplacental initiation of NMRI mice with 7,12-dimethylbenz[a]anthracene during gestation days 6--20 and postnatal treatment of the F1-generation with the phorbol ester 12-O-tetradecanoylphorbol-13-acetate: tumor incidence in organs other than the skin.在妊娠第6至20天用7,12 - 二甲基苯并[a]蒽对NMRI小鼠进行经胎盘起始处理,并对F1代小鼠产后用佛波酯12 - O - 十四酰佛波醇 - 13 - 乙酸酯进行处理:皮肤以外器官的肿瘤发生率
Carcinogenesis. 1981;2(11):1087-94. doi: 10.1093/carcin/2.11.1087.
2
7,12-Dimethylbenz[a]anthracene/12-O-tetradecanoyl-phorbol-13-acetate-mediated skin tumor initiation and promotion in male Sprague-Dawley rats.7,12-二甲基苯并[a]蒽/12-O-十四烷酰佛波醇-13-乙酸酯介导的雄性斯普拉格-道利大鼠皮肤肿瘤启动和促进
Carcinogenesis. 1982;3(7):785-9. doi: 10.1093/carcin/3.7.785.
3
Skin tumor formation in the European hamster (Cricetus cricetus L.) after topical initiation with 7,12-dimethylbenz[a]anthracene (DMBA) and promotion with 12-O-tetradecanoylphorbol-13-acetate (TPA).用7,12-二甲基苯并[a]蒽(DMBA)进行局部启动并随后用12-O-十四烷酰佛波醇-13-乙酸酯(TPA)进行促癌后,欧洲仓鼠(Cricetus cricetus L.)皮肤肿瘤的形成。
Carcinogenesis. 1984 Apr;5(4):521-4. doi: 10.1093/carcin/5.4.521.
4
Diaplacental carcinogenesis: initiation with the carcinogens dimethylbenzanthracene (DMBA) and urethane during fetal life and postnatal promotion with the phorbol ester TPA in a modified 2-stage Berenblum/Mottram experiment.经胎盘致癌作用:在改良的两阶段贝伦布卢姆/莫特拉姆实验中,在胎儿期用致癌物二甲基苯并蒽(DMBA)和氨基甲酸乙酯引发,产后用佛波酯TPA促进。
Virchows Arch A Pathol Anat Histol. 1976 Nov 22;372(1):29-38. doi: 10.1007/BF00429714.
5
Systemic two-stage carcinogenesis in the epithelium of the forestomach of mice using 7,12-dimethylbenz(a)anthracene as initiator and the phorbol ester 12-O-tetradecanoylphorbol-13-acetate as promoter.以7,12-二甲基苯并(a)蒽为引发剂、佛波酯12-O-十四酰佛波醇-13-乙酸酯为促癌剂,在小鼠前胃上皮细胞中进行的系统性两阶段致癌作用。
Cancer Res. 1979 Apr;39(4):1293-7.
6
Two-stage skin carcinogenesis by systemic initiation of pregnant mice with 7,12-dimethylbenz(a)anthracene during gestation days 6-20 and postnatal promotion of the F 1-generation with the phorbol ester 12-tetradecanoylphorbol-13-acetate.通过在妊娠第6至20天用7,12 - 二甲基苯并(a)蒽对怀孕小鼠进行全身启动,并在F1代出生后用佛波酯12 - 十四酰佛波醇-13 - 乙酸酯进行促进,诱导两阶段皮肤癌发生。
J Cancer Res Clin Oncol. 1980;98(3):267-75. doi: 10.1007/BF00410789.
7
Two-stage carcinogenesis in NMRI mice: intravaginal application of 7,12-dimethylbenz[a]anthracene as initiator followed by the phorbol ester 12-O-tetradecanoylphorbol-13-acetate as promoter.NMRI小鼠的两阶段致癌作用:经阴道应用7,12-二甲基苯并[a]蒽作为引发剂,随后应用佛波酯12-O-十四烷酰佛波醇-13-乙酸酯作为促癌剂。
Carcinogenesis. 1980 Aug;1(8):707-13. doi: 10.1093/carcin/1.8.707.
8
Dehydroepiandrosterone (DHEA) and 3 beta-methylandrost-5-en-17-one: inhibitors of 7,12-dimethylbenz[a]anthracene (DMBA)-initiated and 12-O-tetradecanoylphorbol-13-acetate (TPA)-promoted skin papilloma formation in mice.脱氢表雄酮(DHEA)和3β-甲基雄甾-5-烯-17-酮:7,12-二甲基苯并[a]蒽(DMBA)引发及12-O-十四烷酰佛波醇-13-乙酸酯(TPA)促进的小鼠皮肤乳头瘤形成的抑制剂。
Carcinogenesis. 1984 Apr;5(4):463-6. doi: 10.1093/carcin/5.4.463.
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Effect of the promoter 12-O-tetradecanoylphorbol-13-acetate on the evolution of carcinogen-altered cell populations in tracheas initiated with 7,12-dimethylbenz(a)anthracene.启动子12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯对用7,12 - 二甲基苯并(a)蒽启动的气管中致癌物改变的细胞群体演变的影响。
Cancer Res. 1983 Apr;43(4):1461-6.
10
Chemical carcinogenesis by the two-stage protocol in the skin Mastomys natalensis (Muridae) using topical initiation with 7,12-dimethylbenz(a)anthracene and topical promotion with 12-0-tetradecanoylphorbol-13-acetate.使用7,12-二甲基苯并(a)蒽进行局部启动和12-O-十四酰佛波醇-13-乙酸酯进行局部促进,通过两阶段方案在南非多乳鼠(鼠科)皮肤中诱导化学致癌作用。
Virchows Arch B Cell Pathol Incl Mol Pathol. 1981;38(1):13-21. doi: 10.1007/BF02892799.

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