[Effect of 5-Aza-dC on FHIT gene expression in hepatocellular carcinoma cell line HepG2].

Hong-Li Li, Wei-Dong Zhang, Wen-Tong Li, Chong-Gao Yin
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引用次数: 1

Abstract

Background and objective: FHIT gene methylation leads to down-regulation of its expression in hepatocellular carcinoma (HCC) cells. This study was to detect the expression of FHIT mRNA and protein in HCC cell line HepG2 after treatment of methylase inhibitor 5-Aza-2'-deoxycytidine (5-Aza-dC), and observe the effect of 5-Aza-dC on the proliferation of HepG2 cells.

Methods: HepG2 cells were treated with 5-Aza-dC. Methylation of FHIT in HepG2 cells was detected by methylation-specific polymerase chain reaction (MSP). FHIT mRNA expression was detected by reverse transcription-polymerase chain reaction (RT-PCR). FHIT protein expression was detected by immunohistochemistry and Western blot. Cell proliferation was detected by MTT assay.

Results: Before treatment of 5-Aza-dC, FHIT gene methylation was detected in HepG2 cells, while no FHIT mRNA and protein expression was detected. The hypermethylation of FHIT gene in HepG2 cells was effectively reversed after treatment of 5-Aza-dC. When HepG2 cells were treated with 1.0, 2.0, and 4.0 micromol/L of 5-Aza-dC for 48 h, the mRNA levels of FHIT were 0.80+/-0.32, 1.41+/-0.54, and 1.51+/-0.61, respectively; the protein levels of FHIT were 0.33+/-0.20, 1.00+/-0.26, and 1.12+/-0.38, respectively. Cell proliferation was significantly inhibited after being treated with 5-Aza-dC.

Conclusion: 5-Aza-dC can reverse the abnormal methylation of FHIT gene, activate the silenced gene and induce FHIT mRNA and protein expression in HepG2 cells.

5-Aza-dC对肝癌细胞系HepG2中FHIT基因表达的影响
背景与目的:FHIT基因甲基化导致其在肝细胞癌(HCC)细胞中的表达下调。本研究旨在检测甲基化酶抑制剂5-Aza-2′-脱氧胞苷(5-Aza-dC)处理肝癌细胞株HepG2后FHIT mRNA和蛋白的表达,并观察5-Aza-dC对HepG2细胞增殖的影响。方法:用5-Aza-dC处理HepG2细胞。甲基化特异性聚合酶链反应(MSP)检测HepG2细胞中FHIT的甲基化。采用逆转录聚合酶链反应(RT-PCR)检测FHIT mRNA表达。免疫组织化学和Western blot检测FHIT蛋白表达。MTT法检测细胞增殖情况。结果:5-Aza-dC处理前,HepG2细胞检测到FHIT基因甲基化,未检测到FHIT mRNA和蛋白的表达。5-Aza-dC可有效逆转HepG2细胞中FHIT基因的高甲基化。1.0、2.0和4.0微mol/L 5-Aza-dC作用HepG2细胞48 h后,FHIT mRNA表达水平分别为0.80+/-0.32、1.41+/-0.54和1.51+/-0.61;FHIT蛋白水平分别为0.33+/-0.20、1.00+/-0.26、1.12+/-0.38。5-Aza-dC处理后,细胞增殖明显受到抑制。结论:5-Aza-dC可逆转FHIT基因异常甲基化,激活沉默基因,诱导HepG2细胞中FHIT mRNA和蛋白的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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