Elmets C A, Khan W A, Klemme J C, Mukhtar H
Department of Dermatology, University Hospitals of Cleveland, Ohio.
Biochem Biophys Res Commun. 1988 Feb 29;151(1):148-52. doi: 10.1016/0006-291x(88)90571-2.
7,12-dimethylbenz(a)anthracene (DMBA) is a polyaromatic hydrocarbon with potent mutagenic, carcinogenic and immunomodulatory activities. It has been postulated that the immunosuppressive effects of DMBA may contribute to the carcinogenicity of this agent. We investigated this issue by examining whether the pre-administration of DMBA at one skin site would augment its carcinogenic activity at a distant skin site. In animals placed on a cutaneous chemical carcinogenesis protocol to the skin of the back, pre-sensitization with DMBA to the abdomen augmented skin tumorigenicity whether the tumor data are considered as cumulative number of tumors, percent of mice with tumors, number of tumors per mouse, or numbers of tumors per tumor bearing mouse as a function of weeks on test. These data demonstrate that pre-treatment with DMBA augments its skin tumorigenicity by impairing immunological surveillance.
7,12-二甲基苯并(a)蒽(DMBA)是一种具有强大诱变、致癌和免疫调节活性的多环芳烃。据推测,DMBA的免疫抑制作用可能促成了该物质的致癌性。我们通过检查在一个皮肤部位预先给予DMBA是否会增强其在远处皮肤部位的致癌活性来研究这个问题。在接受背部皮肤化学致癌方案的动物中,用DMBA对腹部进行预先致敏会增强皮肤致瘤性,无论肿瘤数据是按累积肿瘤数量、患肿瘤小鼠的百分比、每只小鼠的肿瘤数量,还是按作为试验周数函数的每只荷瘤小鼠的肿瘤数量来计算。这些数据表明,DMBA预处理通过损害免疫监视增强了其皮肤致瘤性。