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地塞米松敏感性降低的大鼠肝癌细胞中甲胎蛋白合成的激活

Activation of alpha-fetoprotein synthesis in rat hepatoma cells with reduced sensitivity to dexamethasone.

作者信息

Venetianer A, Poliard A, Poiret M, Erdös T, Hermesz E, Sala-Trepat J M

出版信息

Differentiation. 1986;32(2):148-56. doi: 10.1111/j.1432-0436.1986.tb00567.x.

Abstract

The Faza 967 'differentiated', dexamethasone (DEX)-sensitive cell line of Reuber rat hepatoma cells does not synthesize detectable amounts of alpha-fetoprotein (AFP), whereas it does produce albumin. AFP production was activated in 'differentiated' variants of Faza 967 cells with reduced glucocorticoid sensitivity upon culture for several months in the presence of high concentrations of dexamethasone. The stability of AFP production differed among the variants, while albumin synthesis did not change, thus indicating that the regulation of these two genes is not co-ordinated. Using molecular hybridization techniques, we found that the AFP message could not be detected in the non-AFP-producing cells, suggesting that the lack of AFP synthesis most probably originates from a transcriptional block of the AFP gene. AFP-producing and non-AFP-producing variants of Faza 967 cells constitute a valuable model system for studying the regulatory mechanisms involved in the activation and inactivation of the gene coding for the oncodevelopmental protein, AFP.

摘要

Faza 967“分化型”、地塞米松(DEX)敏感的鲁伯大鼠肝癌细胞系不合成可检测量的甲胎蛋白(AFP),但能产生白蛋白。在高浓度地塞米松存在下培养数月后,糖皮质激素敏感性降低的Faza 967细胞“分化型”变体中,AFP的产生被激活。不同变体中AFP产生的稳定性有所不同,而白蛋白合成没有变化,这表明这两个基因的调控并非协同进行。使用分子杂交技术,我们发现在不产生AFP的细胞中检测不到AFP信息,这表明AFP合成的缺乏很可能源于AFP基因的转录阻滞。Faza 967细胞产生AFP和不产生AFP的变体构成了一个有价值的模型系统,用于研究参与肿瘤发育蛋白AFP编码基因激活和失活的调控机制。

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