首页> 外文期刊>World Journal of Gastroenterology >Altered profiles of nuclear matrix proteins during the differentiation of human gastric mucous adenocarcinoma MGc80-3 cells.
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Altered profiles of nuclear matrix proteins during the differentiation of human gastric mucous adenocarcinoma MGc80-3 cells.

机译:人胃黏膜腺癌MGc80-3细胞分化过程中核基质蛋白的分布改变。

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AIM: To find and identify specific nuclear matrix proteins associated with proliferation and differentiation of carcinoma cells, which will be potential markers for cancer diagnosis and targets in cancer therapy. METHODS: Nuclear matrix proteins were selectively extracted from MGc80-3 cells treated with or without hexamethylamine bisacetamide (HMBA), and subjected to 2-D gel electrophoresis. The resulted protein patterns were analyzed by Melanie software. Spots of nuclear matrix proteins differentially expressed were excised and subjected to in situ digestion with trypsin. Peptide masses were obtained by matrix-assisted laser-desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS) analysis and submitted for database searching using Mascot tool. RESULTS: The MGc80-3 cells were induced into differentiation by HMBA. There were 22 protein spots which changed remarkably in the nuclear matrix, from differentiation of MGc80-3 cells compared to control. Eleven of which were identified. Seven proteins - actin, prohibitin, porin 31HL, heterogeneous nuclear ribonucleoprotein A2/B1, vimentin, ATP synthase, and heat shock protein 60 were downregulated, whereas three proteins - heat shock protein gp96, heat shock protein 90-beta, and valosin-containing protein were upregulated, and the oxygen-regulated protein was only found in the differentiated MGc80-3 cells. CONCLUSION: The induced differentiation of carcinoma cells is accompanied by the changes of nuclear matrix proteins. Further characterization of those proteins will show the mechanism of cellular proliferation and differentiation, as well as cancer differentiation.
机译:目的:寻找并鉴定与癌细胞增殖和分化有关的特定核基质蛋白,这些蛋白将成为癌症诊断的潜在标志物和癌症治疗的靶标。方法:从经或不经六甲胺双乙酰胺(HMBA)处理的MGc80-3细胞中选择性提取核基质蛋白,并进行2-D凝胶电泳。通过Melanie软件分析所得的蛋白质模式。切下差异表达的核基质蛋白斑点,并用胰蛋白酶原位消化。通过基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)分析获得肽质量,并使用Mascot工具提交数据库搜索。结果:HMBA诱导MGc80-3细胞分化。与对照相比,从MGc80-3细胞的分化来看,在核基质中有22个蛋白点发生了显着变化。确定了其中的11个。七个蛋白-肌动蛋白,抑制素,孔蛋白31HL,异质核糖核糖核蛋白A2 / B1,波形蛋白,ATP合酶和热休克蛋白60被下调,而三个蛋白-热休克蛋白gp96,热休克蛋白90-beta和含缬氨酸蛋白质被上调,而氧调节的蛋白质仅在分化的MGc80-3细胞中被发现。结论:癌细胞的诱导分化伴随着核基质蛋白的变化。这些蛋白质的进一步表征将显示细胞增殖和分化以及癌症分化的机制。

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