Hasenson M, Hartley-Asp B, Kihlfors C, Lundin A, Gustafsson J A, Pousette A
Prostate. 1985;7(2):183-94. doi: 10.1002/pros.2990070208.
The use of ATP content as a measurement for cell growth was evaluated in the LNCaP prostatic cancer cell line. ATP content was found to correlate well with cell counts and was an easy and reliable method for following the effect of substances on cell growth. During cultivation for 9 days no effect on cell counts or ATP content could be seen when testosterone (10(-10) to 10(-6) M), estradiol-17 beta (10(-10) to 10(-5) M), 5 alpha-DHT (10(-9) to 10(-6) M), prolactin, vitamin A, or antiandrogen was added to the cell medium in different combinations. However, a weak positive effect was seen on the mitotic index when 10 or 100 nM 5 alpha-DHT was added to the cells, whereas 1 microM 5 alpha-DHT inhibited cell growth. Thus despite the fact that this LNCaP line contained 16 fmol androgen receptor/mg protein (Kd 0.6 nM), it is unresponsive to hormones and should be designated LNCaP-r (resistant). Chromosome analysis revealed that a shift in the modal chromosome number had occurred from the original LNCaP line, which could account for the lack of hormonal sensitivity.
在LNCaP前列腺癌细胞系中评估了将ATP含量用作细胞生长测量指标的情况。发现ATP含量与细胞计数密切相关,是一种追踪物质对细胞生长影响的简便可靠方法。在9天的培养过程中,当以不同组合向细胞培养基中添加睾酮(10(-10)至10(-6)M)、雌二醇-17β(10(-10)至10(-5)M)、5α-双氢睾酮(10(-9)至10(-6)M)、催乳素、维生素A或抗雄激素时,未观察到对细胞计数或ATP含量的影响。然而,当向细胞中添加10或100 nM的5α-双氢睾酮时,观察到对有丝分裂指数有微弱的正向影响,而1 μM的5α-双氢睾酮则抑制细胞生长。因此,尽管该LNCaP细胞系含有16 fmol雄激素受体/毫克蛋白(解离常数0.6 nM),但它对激素无反应,应被指定为LNCaP-r(抗性)。染色体分析显示,与原始LNCaP细胞系相比,众数染色体数发生了变化,这可能解释了其缺乏激素敏感性的原因。