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机构地区:[1]北京医科大学生化教研室,北京医科大学天然药物及仿生药物国家重点实验室
出 处:《生物化学杂志》1994年第1期21-24,共4页
摘 要:本文利用Northern印迹分析技术研究了完全致癌物二甲基苯蒽(DMBA)对小鼠表皮鸟氨酸脱羧酶(ODC)mRNA和转化生长因子β(TGF-β)mRNA水平的影响。DMBA在15μg和900μg剂量下一次涂用于小鼠皮肤,可使表皮ODCmRNA和TGF-βmRNA表达增加。ODCmRNA为单一的2.0kb大小的条带,其表达在在36h时最为明显。而TGF-βmRNA大小为2.5kb和1.9kb,其表达在36h时最高,到48h几乎降至正常,但在72h又有增加。ODC和TGF-β可能在DMBA诱癌过程中起重要作用。The effects of 7,12-dimethylbena[a] anthracene(DMBA) on the mRNA levels of ornithine decarboxylase(ODC) and transforming growth factor-β (TGF-β) in mouse epidermis were studied by Northern blotting in this paper. A single topical treatment of mouse skin with DMBA at doses of 150μg and 900 μg resulted in increased expressions of ODC and TGF-β mRNA. ODC mRNA was a single major band of 2. 0 kb in size. Its expression appeared to be maximal at 36h after treatment and returned to near control level after 96h.TGF-β mRNA exhibited two bands of 2. 5kb and 1.9kb in size. Its level reached maximum at about 36h and then declined to normal level at 48h. A second, less intense maximum was observed at about 72h after treatment. These results indicate that ODC and TG-βmay play roles in DMBA-induced carcinogenesis.
分 类 号:R730.231.1[医药卫生—肿瘤]
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