Slaga T J, Thompson S, Schwarz J A
J Invest Dermatol. 1977 May;68(5):307-9. doi: 10.1111/1523-1747.ep12494574.
The binding of the potent anticarcinogenic agent, dexamethasone, to mouse epidermal and dermal subcellular fractions was investigated. When applied to mouse skin, 3H-labeled dexamethasone remained associated, after extensive dialysis, with epidermal and dermal cytosol, microsomes, microsomes, mitochondria, and chromatin. The specific activity of dexamethasone binding to these fractions was from 2 to 5 times as high in the epidermis as in the dermis. Epidermal chromatin had the highest specific activity fo binding. Dexamethasone was not associated with the cytosol protein receptor which was previously found to specifically bind tumor promoters and polycyclic hydrocarbon carcinogens.
研究了强效抗癌剂地塞米松与小鼠表皮和真皮亚细胞组分的结合情况。将3H标记的地塞米松应用于小鼠皮肤后,经过大量透析,它仍与表皮和真皮的胞质溶胶、微粒体、线粒体及染色质相关联。地塞米松与这些组分结合的比活性在表皮中是真皮中的2至5倍。表皮染色质具有最高的结合比活性。地塞米松与先前发现能特异性结合肿瘤启动子和多环烃致癌物的胞质溶胶蛋白受体无关。