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首页> 外文期刊>Medical oncology >{2-((3-Carboxy-1-oxopropyl) amino)-2-deoxy-D-Glucose} suppresses proliferation and induces apoptosis in the human esophageal cancer cell line.
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{2-((3-Carboxy-1-oxopropyl) amino)-2-deoxy-D-Glucose} suppresses proliferation and induces apoptosis in the human esophageal cancer cell line.

机译:{2-((3-羧基-1-氧丙基)氨基)-2-脱氧-D-葡萄糖}在人食道癌细胞系中抑制增殖并诱导凋亡。

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摘要

The aim of this study was to investigate the molecular mechanisms of apoptosis induced by {2-[(3-Carboxy-1-oxopropyl) amino]-2-deoxy-D-Glucose} (COPADG) in the esophageal cancer cell line Eca-109 and to establish a relationship between the rate of apoptosis and Fas and Bcl-2 protein expression. Eca-109 cells were cultured under standard condition. Cell growth was measured by MTT assay. Apoptosis and cell proliferation were determined by flow cytometry. Expressions of apoptosis-regulated genes Fas and Bcl-2 were detected by immunohistochemical methods and image analysis. COPADG dose- and time-dependently inhibited the growth of Eca-109 cells in vitro. Incubation of Eca-109 cells with 40 mumol/l of COPADG for 48 h induced significant apoptosis. After drug treatment, Fas protein expression was increased, while Bcl-2 protein expression was decreased. COPADG is able to induce apoptosis in the esophageal cancer cell line Eca-109. The mechanism of apoptosis in these cells may be related to up-regulation of Fas gene expression and the down-regulation of Bcl-2, which may serve as the experimental evidence for development of new drugs for the non-surgical management of human esophageal cancer.
机译:这项研究的目的是研究由{2-[(3-羧基-1-氧丙基)氨基] -2-脱氧-D-葡萄糖}(COPADG)诱导的食管癌细胞株Eca-凋亡的分子机制。 109并建立凋亡率与Fas和Bcl-2蛋白表达之间的关系。在标准条件下培养Eca-109细胞。通过MTT测定法测量细胞生长。通过流式细胞术确定细胞凋亡和细胞增殖。通过免疫组织化学方法和图像分析检测凋亡调控基因Fas和Bcl-2的表达。 COPADG在体外剂量和时间依赖性抑制Eca-109细胞的生长。将Eca-109细胞与40μmol/ l的COPADG孵育48小时可诱导明显的凋亡。药物治疗后,Fas蛋白表达增加,而Bcl-2蛋白表达减少。 COPADG能够在食道癌细胞系Eca-109中诱导凋亡。这些细胞凋亡的机制可能与Fas基因表达的上调和Bcl-2的下调有关,这可以作为开发用于非手术治疗食管癌的新药的实验证据。 。

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