Goerttler K, Loehrke H, Hesse B, Pyerin W G
Carcinogenesis. 1982;3(7):791-5. doi: 10.1093/carcin/3.7.791.
Initiation of dermal melanocytes by 7,12-dimethylbenz[a]-anthracene (DMBA) in the dorsal skin of Syrian golden hamsters was investigated for its sensitivity to inhibition by 7,8-benzoflavone (BF). Initiation was carried out by a single intragastric application of DMBA (50 mg/kg body weight) and melanoma development pursued with or without subsequent promotion through repeated topical administration of 12-O-tetradecanoylphorbol-13-acetate (40 nmol/animal, 3 X weekly). A single intragastric application of BF (200 mg/kg body weight) 2 h prior to DMBA resulted in a suppression of melanoma yields by approximately 70%. Further, there were indications that BF generally causes a decrease of melanoma rates and an increase of survival rates. The study provides a first mechanistic concept for melanoma initiation by DMBA. It shows that metabolic activation of DMBA (i) is prerequisite to initiation and (ii) has a similar molecular basis as in other target cells of DMBA, the essential pathway including the cytochrome P-448-dependent monooxygenase system.
研究了7,12-二甲基苯并[a]蒽(DMBA)对叙利亚金仓鼠背部皮肤真皮黑素细胞的启动作用及其对7,8-苯并黄酮(BF)抑制作用的敏感性。通过单次胃内给予DMBA(50mg/kg体重)进行启动,并通过重复局部给予12-O-十四烷酰佛波醇-13-乙酸酯(40nmol/动物,每周3次)进行或不进行后续促癌处理来追踪黑色素瘤的发展。在给予DMBA前2小时单次胃内给予BF(200mg/kg体重)可使黑色素瘤产量降低约70%。此外,有迹象表明BF通常会导致黑色素瘤发生率降低和存活率提高。该研究为DMBA引发黑色素瘤提供了首个机制概念。研究表明,DMBA的代谢活化(i)是启动的先决条件,(ii)与DMBA的其他靶细胞具有相似的分子基础,基本途径包括细胞色素P-448依赖性单加氧酶系统。