首页> 外文期刊>World Journal of Gastroenterology >Effect of c-fos antisense probe on prostaglandin E(2)-induced upregulation of vascular endothelial growth factor mRNA in human liver cancer cells.
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Effect of c-fos antisense probe on prostaglandin E(2)-induced upregulation of vascular endothelial growth factor mRNA in human liver cancer cells.

机译:c-fos反义探针对前列腺素E(2)诱导的人肝癌细胞血管内皮生长因子mRNA上调的影响。

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AIM: To examine the effect of prostaglandin E(2) (PGE(2)) on the expression of vascular endothelial growth factor (VEGF) mRNA in the human hepatocellular carcinoma (HCC) HepG2 cells and the possible involvement of c-fos protein in this process. METHODS: Human HCC HepG2 cells were divided into three groups treated respectively with PGE(2), a combination of PGE(2) and c-fos antisense oligodeoxynucleotide (ASO), and PGE(2) plus c-fos sense oligodeoxynucleotide (SO). The expression of VEGF mRNA in HepG2 cells after different treatments was detected by reverse transcriptase-polymerase chain reaction (RT-PCR). The relative expression level of VEGF mRNA in HepG2 cells in each group was measured. RESULTS: Administration of PGE(2) resulted in an increased expression of c-fos and VEGF mRNA in HepG2 cells. The relative expression level of c-fos mRNA reached the peak at 3 h (68.4+/-4.7%) after PGE(2) treatment, which was significantly higher than that at 0 h (20.6+/-1.7%, P<0.01). Whereas, the highest expression level of VEGF mRNA was observed at 6 h (100.5+/-6.1%) after PGE(2) treatment, which was significantly higher than that at 0 h (33.2+/-2.4%, P<0.01). C-fos ASO significantly reduced PGE(2)-induced VEGF mRNA expression in HepG2 cells. CONCLUSION: PGE(2) increases the expression and secretion of VEGF in HCC cells by activating the transcription factor c-fos, promotes the angiogenesis of HCC and plays an important role in the pathogenesis of liver cancer.
机译:目的:研究前列腺素E(2)(PGE(2))对人肝细胞癌(HCC)HepG2细胞中血管内皮生长因子(VEGF)mRNA表达的影响以及c-fos蛋白可能参与了这个过程。方法:将人肝癌HepG2细胞分为三组,分别用PGE(2),PGE(2)和c-fos反义寡脱氧核苷酸(ASO)和PGE(2)加c-fos正义寡脱氧核苷酸(SO)组合处理。通过逆转录聚合酶链反应(RT-PCR)检测不同处理后HepG2细胞中VEGF mRNA的表达。测定各组HepG2细胞中VEGF mRNA的相对表达水平。结果:PGE(2)的使用导致HepG2细胞中c-fos和VEGF mRNA的表达增加。 c-fos mRNA的相对表达水平在PGE(2)处理后3 h达到峰值(68.4 +/- 4.7%),显着高于0 h(20.6 +/- 1.7%),P <0.01 )。而在PGE(2)处理后6 h(100.5 +/- 6.1%)观察到VEGF mRNA的最高表达水平,显着高于0 h(33.2 +/- 2.4%,P <0.01)。 。 C-fos ASO显着降低HepG2细胞中PGE(2)诱导的VEGF mRNA表达。结论:PGE(2)通过激活转录因子c-fos增加肝癌细胞中VEGF的表达和分泌,促进肝癌的血管生成,在肝癌的发病中起重要作用。

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