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布雷菲德菌素A(一种影响神经节苷脂生物合成的药物)诱导人结肠癌细胞发生终末分化和凋亡。

Induction of terminal differentiation and apoptosis in human colonic carcinoma cells by brefeldin A, a drug affecting ganglioside biosynthesis.

作者信息

Nojiri H, Manya H, Isono H, Yamana H, Nojima S

机构信息

Faculty of Pharmaceutical Sciences, Teikyo University, Tsukui-gun, Kanagawa, Japan.

出版信息

FEBS Lett. 1999 Jun 18;453(1-2):140-4. doi: 10.1016/s0014-5793(99)00709-7.

Abstract

An appreciable increase in G(M3) with a concomitant decrease in some neolacto-series gangliosides was observed during differentiation of human colonic carcinoma HCT 116 cells induced by a differentiating agent. When the cells were treated with brefeldin A (BFA), a striking increase in de novo biosynthesis of G(M3) and a decrease in biosynthesis of neolactoseries gangliosides were observed after 6 h. Clear morphological changes to differentiated epithelial cells and an arrest of cells in the G0/G1 phase of the cell cycle were observed after 1 day of treatment. Then the cells were led to apoptosis. This activity was not affected by forskolin, which antagonizes the effects of BFA on protein transport and the Golgi apparatus. These results suggest that the differentiation-inducing activity of BFA might be due to its modulatory effect on ganglioside biosynthesis, and that a specific change in ganglioside pattern is an essential prerequisite for induction of differentiation, providing a novel target for differentiation therapy of cancer.

摘要

在用分化剂诱导人结肠癌HCT 116细胞分化的过程中,观察到G(M3)显著增加,同时一些新乳糖系列神经节苷脂减少。当细胞用布雷菲德菌素A(BFA)处理时,6小时后观察到G(M3)的从头生物合成显著增加,新乳糖系列神经节苷脂的生物合成减少。处理1天后,观察到细胞明显分化为上皮细胞并停滞在细胞周期的G0/G1期。然后细胞发生凋亡。这种活性不受福斯高林的影响,福斯高林可拮抗BFA对蛋白质转运和高尔基体的作用。这些结果表明,BFA的分化诱导活性可能归因于其对神经节苷脂生物合成的调节作用,并且神经节苷脂模式的特定变化是诱导分化的必要前提,为癌症的分化治疗提供了新的靶点。

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