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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Differentially expressed genes from the glioblastoma cell line SHG-44 treated with all-trans retinoic acid in vitro.
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Differentially expressed genes from the glioblastoma cell line SHG-44 treated with all-trans retinoic acid in vitro.

机译:胶质母细胞瘤细胞系SHG-44的差异表达基因在体外经全反式维甲酸处理。

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摘要

Morphology, immunocytochemistry, growth curve assay, and flow cytometry were used to investigate the effects of all-trans retinoic acid (RA) on cell proliferation, cell cycle progression and differentiation of the astrocytoma cell line SHG-44 from glioblastoma multiforme (World Health Organization grade IV). The differentially expressed genes from RA-treated and normal SHG-44 were identified by cDNA microarray after the cell line SHG-44 was treated with 10muM RA for 3 days. Validation of some differentially expressed genes was performed by Northern Blot analysis. The expression of glial fibrillary acidic protein (GFAP) was markedly increased in RA-treated SHG-44 cells. Other changes included a short shuttle shape, small nucleus, decreased karyoplasm proportion, the formation of increased thin cytoplasmic processes, reduced cell growth and a 15% increase in G0/G1 phase cell populations. In addition, 42 known genes were identified with altered expression in our cDNA microarray. There was stable down-regulation of MDM2 and UGB as well as overexpression of SOD2, CSTB, and G3BP when RA-treated SHG-44 was compared with normal SHG-44. RA simultaneously suppressed the proliferation of SHG-44 cells significantly as well as induced differentiation and altered gene expression.
机译:形态学,免疫细胞化学,生长曲线测定和流式细胞仪用于研究全反式维甲酸(RA)对星形胶质母细胞瘤星形细胞瘤细胞SHG-44细胞增殖,细胞周期进程和分化的影响(世界卫生组织四级)。用10μMRA处理细胞系SHG-44 3天后,通过cDNA微阵列鉴定出RA处理过的和正常SHG-44差异表达的基因。通过Northern Blot分析验证一些差异表达的基因。 RA处理的SHG-44细胞中神经胶质纤维酸性蛋白(GFAP)的表达明显增加。其他变化包括短的穿梭形状,小的核,核质比例减少,形成的稀薄细胞质过程,减少的细胞生长以及G0 / G1期细胞群增加15%。此外,在我们的cDNA微阵列中鉴定出42个已知基因的表达发生了改变。当将RA处理的SHG-44与正常SHG-44进行比较时,MDM2和UGB的稳定下调以及SOD2,CSTB和G3BP的过表达。 RA同时显着抑制SHG-44细胞的增殖以及诱导分化和基因表达改变。

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