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[人前列腺癌细胞系的研究:酸性磷酸酶产生能力的评估及性激素对细胞的影响]

[Studies on human prostatic carcinoma cell lines: evaluation of acid phosphatase productivity and effects of sex hormones on the cells].

作者信息

Nakagami Y, Minowa T, Tozuka K, Hiraoka Y, Nakajima H, Ishizaki R, Mastsumoto K

出版信息

Gan To Kagaku Ryoho. 1983 Sep;10(9):1993-9.

PMID:6614935
Abstract

The established cell lines from human prostatic cancer, such as Duke 145, 8PC93, and 19PC93, were examined in terms of their producing activity of acid phosphatase (ACP) and sensitivity to sex hormones. The results obtained are summarized. 1. ACP producing activity ACP was estimated with phenyl phosphate as a substrate. Values of the materials from each of the cells extracted with 5% Triton X-100 were Duke 145 (6.1 u/mg), 8PC93 (40.6 u/mg), and 19PC93 (40.4 u/mg), respectively. Activities of ACP were prohibited by the presence of L-tartrate. Histochemistry of ACP was demonstrated by azo-dye staining procedure, revealing the positive reactions in the cytoplasms of 8PC93 and 19PC93 cells, but weak reaction in duke 145 cells. Disk polyacrylamide gel electrophoresis (D-PAGE) was employed for ACP analysis of the cell extracts with 5% Tryton X-100 treatment. Two main bands were observed near original point and at another point proposed as ACP-2. These ACP positive reactions on the gels were also inhibited by the presence of L-tartrate in staining solution. In the case of Duke 145 cell material, the intensity of the reaction was observed weak in those specific two bands. 2. Hormone effects to the cells The prostatic cancer cells were examined in terms of sensitivity to sex steroid hormones such as androsterone, progesterone, estrone, estradiol, and estriol, by a colony formation method. Fifty percent reduction in colony formation of the 8PC93 and 19PC93 cells was found at the concentration of ca. 1.5 micrograms/ml in the case using progesterone or estrone, or estradiol, while 50% reduction of the Duke 145 cells was observed at 5 micrograms/ml only in a case using progesterone.

摘要

对来自人类前列腺癌的既定细胞系,如杜克145、8PC93和19PC93,就其酸性磷酸酶(ACP)的产生活性和对性激素的敏感性进行了检测。现将所得结果总结如下。1. ACP产生活性 以磷酸苯酯为底物估算ACP。用5% Triton X-100提取的各细胞物质的值分别为:杜克145(6.1单位/毫克)、8PC93(40.6单位/毫克)和19PC93(40.4单位/毫克)。L-酒石酸盐的存在会抑制ACP的活性。通过偶氮染料染色法进行ACP的组织化学检测,结果显示8PC93和19PC93细胞的细胞质呈阳性反应,而杜克145细胞的反应较弱。采用圆盘聚丙烯酰胺凝胶电泳(D-PAGE)对经5%曲通X-100处理的细胞提取物进行ACP分析。在原点附近和另一个被认为是ACP-2的点附近观察到两条主要条带。染色液中L-酒石酸盐的存在也会抑制凝胶上这些ACP阳性反应。就杜克145细胞物质而言,在这两条特定条带中观察到反应强度较弱。2. 激素对细胞的影响 通过集落形成法检测前列腺癌细胞对雄酮、孕酮、雌酮、雌二醇和雌三醇等性甾体激素的敏感性。在使用孕酮、雌酮或雌二醇的情况下,当浓度约为1.5微克/毫升时,8PC93和19PC93细胞的集落形成减少50%,而仅在使用孕酮的情况下,当浓度为5微克/毫升时,杜克145细胞的集落形成减少50%。

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