Alidina R, Kikuchi M, Kashima M, Epstein J H, Fukuyama K
Department of Dermatology, University of California, San Francisco 94143.
Exp Mol Pathol. 1988 Aug;49(1):118-27. doi: 10.1016/0014-4800(88)90026-3.
Squamous cell carcinomas (SCC) were experimentally produced in hairless mouse skin, and cysteine protease and its inhibitor were simultaneously purified from extracts of 1 g of tissue of SCC and normal skin. Activity of cysteine proteinases, Mr greater than 50,000 and Mr 28,000, increased in SCC compared to those in normal skin. SCC also showed elevation of cysteine proteinase inhibitor activity and Mr 13,000 and Mr 82,000 inhibitors were purified. Mr 13,000 inhibitor was found to have biochemical properties which were the same as those of the inhibitor present in normal skin. Mr 82,000 inhibitor was not detectable in normal skin and it differed from a serum inhibitor with a similar Mr in terms of activity and stability at acidic pH. The findings suggest that the increased activity of both cysteine proteases and endogenous inhibitors may be involved in the regulatory mechanisms of malignant cell metabolism and tissue remodeling associated with SCC development.
在无毛小鼠皮肤中通过实验诱导产生鳞状细胞癌(SCC),并同时从1克SCC组织和正常皮肤组织的提取物中纯化半胱氨酸蛋白酶及其抑制剂。与正常皮肤相比,Mr大于50,000和Mr 28,000的半胱氨酸蛋白酶活性在SCC中有所增加。SCC中半胱氨酸蛋白酶抑制剂活性也升高,并纯化出了Mr 13,000和Mr 82,000的抑制剂。发现Mr 13,000抑制剂具有与正常皮肤中存在的抑制剂相同的生化特性。在正常皮肤中未检测到Mr 82,000抑制剂,并且在酸性pH条件下其活性和稳定性与具有相似Mr的血清抑制剂不同。这些发现表明,半胱氨酸蛋白酶和内源性抑制剂活性的增加可能参与了与SCC发生相关的恶性细胞代谢和组织重塑的调节机制。