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小鼠皮肤反复损伤促进表皮癌发生

Promotion of epidermal carcinogenesis by repeated damage to mouse skin.

作者信息

Argyris T S

出版信息

Am J Ind Med. 1985;8(4-5):329-37. doi: 10.1002/ajim.4700080412.

DOI:10.1002/ajim.4700080412
PMID:4073030
Abstract

Chemically induced epidermal carcinogenesis is usually divided into two stages: initiation, which involves the conversion of some epidermal cells into latent neoplastic cells; and promotion, which results in tumors. The hallmark of chemical promoters is epidermal hyperplasia. The hyperplasia caused by a strong promoter, such as 12-O-tetradecanoylphorbol-13-acetate (TPA), differs morphologically from that caused by weak promoters, such as acetic acid and mezerin. The epidermal regeneration that follows abrasion results in a hyperplastic epidermis that resembles the effects of strong promoters. Repeated mechanical injuries are capable of enhancing papillomas and carcinomas in mouse skin initiated with 7,12-dimethylbenzanthracene (DMBA). Thus, a regenerative epidermal hyperplasia appears to be a precondition for tumor promotion. It is highly probable that many epidermal cells are initiated during the lifetime of man. In the work place, repeated mechanical injury could predispose to epidermal neoplasms.

摘要

化学诱导的表皮癌发生通常分为两个阶段

启动阶段,涉及将一些表皮细胞转化为潜伏性肿瘤细胞;以及促进阶段,导致肿瘤形成。化学促进剂的标志是表皮增生。由强促进剂如12-O-十四酰佛波醇-13-乙酸酯(TPA)引起的增生在形态上不同于由弱促进剂如乙酸和密执毒素引起的增生。擦伤后随之而来的表皮再生会导致增生性表皮,类似于强促进剂的作用。反复的机械损伤能够增强用7,12-二甲基苯并蒽(DMBA)启动的小鼠皮肤中的乳头状瘤和癌。因此,再生性表皮增生似乎是肿瘤促进的一个先决条件。很可能在人的一生中许多表皮细胞会被启动。在工作场所,反复的机械损伤可能易患表皮肿瘤。

相似文献

1
Promotion of epidermal carcinogenesis by repeated damage to mouse skin.小鼠皮肤反复损伤促进表皮癌发生
Am J Ind Med. 1985;8(4-5):329-37. doi: 10.1002/ajim.4700080412.
2
Regeneration and the mechanism of epidermal tumor promotion.
Crit Rev Toxicol. 1985;14(3):211-58. doi: 10.3109/10408448509037459.
3
Tumor promotion by abrasion induced epidermal hyperplasia in the skin of mice.小鼠皮肤中磨损诱导的表皮增生对肿瘤的促进作用。
J Invest Dermatol. 1980 Oct;75(4):360-2. doi: 10.1111/1523-1747.ep12531153.
4
Only a subset of 12-O-tetradecanoylphorbol-13-acetate-promoted mouse skin papillomas are promotable by benzoyl peroxide.仅一部分由12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯诱导的小鼠皮肤乳头瘤可被过氧化苯甲酰促进。
Mutat Res. 2004 Apr 14;548(1-2):35-45. doi: 10.1016/j.mrfmmm.2003.12.017.
5
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.
6
Enhancement of mezerein-promoted papilloma formation by treatment with 12-O-tetradecanoylphorbol-13-acetate or mezerein prior to initiation.在引发之前用12-O-十四酰佛波醇-13-乙酸酯或芫花素处理可增强芫花素促进的乳头瘤形成。
Carcinogenesis. 1988 Mar;9(3):405-10. doi: 10.1093/carcin/9.3.405.
7
Differential down-regulation of epidermal protein kinase C by 12-O-tetradecanoylphorbol-13-acetate and diacylglycerol: association with epidermal hyperplasia and tumor promotion.12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯和二酰基甘油对表皮蛋白激酶C的差异性下调:与表皮增生和肿瘤促进的关联
Cancer Res. 1990 Sep 15;50(18):5740-5.
8
All-trans retinoic acid protects against conversion of chemically induced and ultraviolet B radiation-induced skin papillomas to carcinomas.全反式维甲酸可预防化学诱导和紫外线B辐射诱导的皮肤乳头状瘤转变为癌。
Carcinogenesis. 1991 Dec;12(12):2325-9. doi: 10.1093/carcin/12.12.2325.
9
Protection against 12-O-tetradecanoylphorbol-13-acetate induced skin-hyperplasia and tumor promotion, in a two-stage carcinogenesis mouse model, by the 2,3-dimethyl-6(2-dimethylaminoethyl)-6H-indolo-[2,3-b]quinoxaline analogue of ellipticine.在两阶段致癌小鼠模型中,椭圆玫瑰树碱的2,3-二甲基-6-(2-二甲基氨基乙基)-6H-吲哚并-[2,3-b]喹喔啉类似物对12-O-十四烷酰佛波醇-13-乙酸酯诱导的皮肤增生和肿瘤促进具有保护作用。
Chem Biol Interact. 1999 Sep 30;122(2):89-106. doi: 10.1016/s0009-2797(99)00117-9.
10
Tumor progression in Sencar mouse skin as a function of initiator dose and promoter dose, duration, and type.Sencar小鼠皮肤肿瘤进展与引发剂剂量、促进剂剂量、持续时间及类型的关系。
Cancer Res. 1988 Dec 15;48(24 Pt 1):7048-54.

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