Anderson K M, Harris J E
Department of Medicine, Rush Medical College, Chicago, Ill.
Clin Physiol Biochem. 1990;8(6):308-13.
5,8,11,14-eicosatetraynoic acid (ETYA), a competitive analogue of arachidonic acid reversibly inhibited human prostate PC3 DNA synthesis at 4 h. This was not due to reduced cellular viability, as judged by several criteria, and resulted in reduced cell numbers at 72 h. Several less specific inhibitors of 5'-lipoxygenase, and A63162, a highly specific inhibitor, reduced labeling of DNA with 3H-thymidine. A23187, a calcium ionophore, reduced DNA synthesis, and ETYA rapidly increased [Ca2+]i measured with the Fura II technique. Comparison of the biochemical events evoked by ETYA and A63162 should identify those required for the downregulation of DNA synthesis.
5,8,11,14-二十碳四炔酸(ETYA),一种花生四烯酸的竞争性类似物,在4小时时可逆地抑制人前列腺PC3细胞的DNA合成。根据多项标准判断,这并非由于细胞活力降低所致,且在72小时时导致细胞数量减少。几种5'-脂氧合酶的非特异性抑制剂以及一种高度特异性抑制剂A63162,均可减少用3H-胸腺嘧啶核苷标记的DNA。钙离子载体A23187可减少DNA合成,并且ETYA可迅速增加用Fura II技术测定的细胞内钙离子浓度([Ca2+]i)。对ETYA和A63162引发的生化事件进行比较,应能确定DNA合成下调所需的那些事件。