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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >Abscisic-acid-induced cellular apoptosis and differentiation in glioma via the retinoid acid signaling pathway
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Abscisic-acid-induced cellular apoptosis and differentiation in glioma via the retinoid acid signaling pathway

机译:脱落酸通过类维生素A酸信号通路诱导神经胶质瘤细胞凋亡和分化

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摘要

Retinoid acid (RA) plays critical roles in regulating differentiation and apoptosis in a variety of cancer cells. Abscisic acid (ABA) and RA are direct derivatives of carotenoids and share structural similarities. Here we proposed that ABA may also play a role in cellular differentiation and apoptosis by sharing a similar signaling pathway with RA that may be involved in glioma pathogenesis. We reported for the first time that the ABA levels were twofold higher in low-grade gliomas compared with high-grade gliomas. In glioma tissues, there was a positive correlation between the ABA levels and the transcription of cellular retinoic acid-binding protein 2 (CRABP2) and a negative correlation between the ABA levels and transcription of fatty acid-binding protein 5 (FABP5). ABA treatment induced a significant increase in the expression of CRABP2 and a decrease in the expression of peroxisome proliferator-activated receptor (PPAR) in glioblastoma cells. Remarkably, both cellular apoptosis and differentiation were increased in the glioblastoma cells after ABA treatment. ABA-induced cellular apoptosis and differentiation were significantly reduced by selectively silencing RAR-α, while RAR-α overexpression exaggerated the ABA-induced effects. These results suggest that ABA may play a role in the pathogenesis of glioma by promoting cellular apoptosis and differentiation through the RA signaling pathway.
机译:维甲酸(RA)在调节多种癌细胞的分化和凋亡中起关键作用。脱落酸(ABA)和RA是类胡萝卜素的直接衍生物,并具有相似的结构。在这里,我们提出了ABA也可能通过与RA共享可能与神经胶质瘤发病机制有关的类似信号通路,在细胞分化和凋亡中发挥作用。我们首次报道低度神经胶质瘤的ABA水平是高度神经胶质瘤的两倍。在神经胶质瘤组织中,ABA水平与细胞视黄酸结合蛋白2(CRABP2)的转录之间呈正相关,而ABA水平与脂肪酸结合蛋白5(FABP5)的转录之间呈负相关。 ABA处理诱导胶质母细胞瘤细胞中CRABP2的表达显着增加,过氧化物酶体增殖物激活受体(PPAR)的表达减少。显着地,在ABA处理后,胶质母细胞瘤细胞中细胞凋亡和分化均增加。通过选择性沉默RAR-α可以显着降低ABA诱导的细胞凋亡和分化,而RAR-α的过表达则夸大了ABA诱导的作用。这些结果表明ABA可能通过促进细胞凋亡和通过RA信号通路的分化而在神经胶质瘤的发病中起作用。

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