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芫花酯素对SENCAR小鼠皮肤肿瘤促进和进展的进一步表征

Further characterization of skin tumor promotion and progression by mezerein in SENCAR mice.

作者信息

Ewing M W, Conti C J, Phillips J L, Slaga T J, DiGiovanni J

机构信息

University of Texas, M. D. Anderson Cancer Center, Science Park Research Division, Smithville 78957.

出版信息

J Natl Cancer Inst. 1989 May 3;81(9):676-82. doi: 10.1093/jnci/81.9.676.

Abstract

This study evaluated the skin tumor-promoting activity of mezerein in SENCAR mice. The effect of initiation dose of 7,12-dimethylbenz(a)anthracene (DMBA) on tumor promotion by mezerein was examined. Excellent dose-response relationships were observed for initiation with DMBA at 0.2-20 micrograms per mouse with mezerein as a complete promoter. None of the mezerein-only promotion groups had papilloma responses similar to those of the corresponding groups receiving two-stage promotion with 12-O-tetradecanoylphorbol-13-acetate (TPA) followed by mezerein, even when a 40-micrograms initiating dose of DMBA was used. The effect delaying promotion with mezerein for 10 weeks was also examined in mice initiated with either 0.2, 2, 20, or 40 micrograms of DMBA per mouse. The 10-week delay led to a slight increase in the number of papillomas per mouse in some but not all treatment groups. Again, none of the delayed-mezerein-treatment groups had papilloma responses similar to those of the corresponding two-stage promotion (TPA-mezerein) groups at any corresponding initiating dose of DMBA. Finally, the progression of papillomas to carcinomas during promotion with mezerein was examined in groups of mice initiated with either 2 or 20 micrograms of DMBA. Higher ratios of carcinomas to papillomas were observed in mice promoted with mezerein than in mice receiving TPA promotion or two-stage promotion (TPA-mezerein). However, the presence of two to four times more papillomas in some mezerein-treated groups did not lead to greater numbers of carcinomas than in the groups with fewer papillomas. The data do not support the idea that spontaneous stage I promotion can be induced by delaying mezerein treatment for 10 weeks. Furthermore, the data suggest that the higher ratio of carcinomas to papillomas observed with mezerein promotion may be a function of the lower tumor burdens obtained after promotion with this compound rather than a specific property of the chemical.

摘要

本研究评估了芫花酯素在SENCAR小鼠中的皮肤肿瘤促进活性。检测了起始剂量的7,12-二甲基苯并(a)蒽(DMBA)对芫花酯素肿瘤促进作用的影响。以芫花酯素作为完全促进剂时,观察到DMBA起始剂量为每只小鼠0.2 - 20微克时具有良好的剂量反应关系。仅使用芫花酯素促进的组中,没有一组出现与相应的先接受12-O-十四酰佛波醇-13-乙酸酯(TPA)然后接受芫花酯素两阶段促进的组相似的乳头状瘤反应,即使使用40微克的起始剂量DMBA也是如此。还在每只小鼠分别用0.2、2、20或40微克DMBA起始的小鼠中检测了用芫花酯素延迟促进10周的效果。10周的延迟导致一些但并非所有治疗组中每只小鼠的乳头状瘤数量略有增加。同样,在任何相应的DMBA起始剂量下,延迟芫花酯素治疗的组中都没有出现与相应的两阶段促进(TPA - 芫花酯素)组相似的乳头状瘤反应。最后,在分别用2或20微克DMBA起始的小鼠组中检测了用芫花酯素促进期间乳头状瘤向癌的进展情况。与接受TPA促进或两阶段促进(TPA - 芫花酯素)的小鼠相比,用芫花酯素促进的小鼠中观察到癌与乳头状瘤的比例更高。然而,在一些芫花酯素处理组中,乳头状瘤数量多两到四倍,但其癌的数量并不比乳头状瘤较少的组更多。这些数据不支持延迟芫花酯素治疗10周可诱导自发的I期促进的观点。此外,数据表明,芫花酯素促进时观察到的癌与乳头状瘤的较高比例可能是该化合物促进后肿瘤负荷较低的结果,而非该化学物质的特定特性。

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