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维生素B6抑制人肝癌细胞系HepG2中白蛋白基因的生长和表达。

Vitamin B6 suppresses growth and expression of albumin gene in a human hepatoma cell line HepG2.

作者信息

Molina A, Oka T, Muńoz S M, Chikamori-Aoyama M, Kuwahata M, Natori Y

机构信息

Department of Nutrition, School of Medicine, University of Tokushima, Japan.

出版信息

Nutr Cancer. 1997;28(2):206-11. doi: 10.1080/01635589709514576.

Abstract

The effect of vitamin B6 on the growth of a human hepatoma cell line HepG2 in culture was studied. The growth of HepG2 cells and protein synthesis were almost completely inhibited in medium supplemented with 5 mM pyridoxine. Pyridoxal was as effective as pyridoxine, but pyridoxamine showed no inhibitory action. The growth inhibition of HepG2 cells by pyridoxine was accompanied by a marked inhibition of secretion of plasma proteins, particularly albumin. Northern blot analysis of albumin mRNA showed that pyridoxine caused a rapid decrease in the expression of albumin gene. The electron-microscopic examination of pyridoxine-treated HepG2 cells revealed a smoothing of nuclear membrane, a decrease in the number of nucleoli, and an appearance of aggregated heterochromatin structures. These morphological features are compatible with the depressed transcriptional activity in the pyridoxine-treated cells. The mechanism by which vitamin B6 exerts its inhibitory effect was discussed in terms of our recent finding that vitamin B6 modulates expression of albumin gene by inactivating tissue-specific DNA-binding proteins. Binding of pyridoxal phosphate with tissue-specific transcription factors may reduce the capacity of these factors to interact with the regulatory region of albumin gene, resulting in the inhibition of the gene expression.

摘要

研究了维生素B6对培养的人肝癌细胞系HepG2生长的影响。在添加5 mM吡哆醇的培养基中,HepG2细胞的生长和蛋白质合成几乎完全受到抑制。吡哆醛与吡哆醇的效果相同,但吡哆胺没有抑制作用。吡哆醇对HepG2细胞的生长抑制伴随着血浆蛋白尤其是白蛋白分泌的显著抑制。白蛋白mRNA的Northern印迹分析表明,吡哆醇导致白蛋白基因表达迅速下降。对经吡哆醇处理的HepG2细胞进行电子显微镜检查发现,核膜变得平滑,核仁数量减少,出现聚集的异染色质结构。这些形态学特征与经吡哆醇处理的细胞中降低的转录活性相符。根据我们最近的发现,即维生素B6通过使组织特异性DNA结合蛋白失活来调节白蛋白基因的表达,讨论了维生素B6发挥其抑制作用的机制。磷酸吡哆醛与组织特异性转录因子的结合可能会降低这些因子与白蛋白基因调控区域相互作用的能力,从而导致基因表达受到抑制。

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