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首页> 外文期刊>Oncology letters >Loss of GATA5 expression due to gene promoter methylation induces growth and colony formation of hepatocellular carcinoma cells
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Loss of GATA5 expression due to gene promoter methylation induces growth and colony formation of hepatocellular carcinoma cells

机译:由于基因启动子甲基化导致的GATA5表达缺失会诱导肝癌细胞的生长和集落形成

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摘要

GATA5 is a transcription factor that is capable of suppressing the development of various types of human cancer. The present study investigated the expression of GATA5 and GATA4, and examined their roles in the proliferation and colony formation ability of hepatocellular carcinoma (HCC) tissues and cells. The GATA4 and GATA5 expression levels and gene promoter methylation of HCC tissue samples from 38 patients and HCC cell lines were analyzed using reverse transcription-polymerase chain reaction (RT-PCR) and methylation-specific PCR (MSP), respectively. The effects of GATA4 and GATA5 overexpression on the proliferation and colony forming ability of HCC cells were also assessed using cell viability and colony formation assays. A luciferase reporter assay was utilized to investigate the transcriptional interaction of GATA4 and GATA5 with canonical Wnt signaling. The results indicated that the expression levels of GATA4 and GATA5 were lost or reduced following methylation of gene promoters in HCC tissues and cell lines. Treatment with a demethylating agent, 5-aza-2'-deoxycytidine (5-AZA), restored GATA4 and GATA5 expression in HCC cell lines. Furthermore, methylation of the GATA5 prothoter was observed to be associated with the age of patients exhibiting HCC. Restoration of GATA4 and GATA5 expression inhibited colony formation and induced apoptosis of HCC cells in vitro. The present study concluded that the expression levels of GATA4 and GATA5 were reduced in HCC tissues and cell lines. Treatment with 5-AZA restored GATA4 and GATA5 expression in HCC cell lines, suppressing tumor cell growth and colony formation, as well as inducing apoptosis.
机译:GATA5是一种转录因子,能够抑制各种类型的人类癌症的发展。本研究调查了GATA5和GATA4的表达,并探讨了它们在肝细胞癌(HCC)组织和细胞的增殖和集落形成能力中的作用。分别使用逆转录聚合酶链反应(RT-PCR)和甲基化特异性PCR(MSP)分析了来自38位患者和HCC细胞系的HCC组织样品的GATA4和GATA5表达水平以及基因启动子甲基化。还使用细胞活力和集落形成测定法评估了GATA4和GATA5过表达对HCC细胞增殖和集落形成能力的影响。萤光素酶报告基因测定被用于研究GATA4和GATA5与经典Wnt信号传导的转录相互作用。结果表明,在肝癌组织和细胞系中基因启动子甲基化后,GATA4和GATA5的表达水平丢失或降低。用脱甲基剂5-氮杂-2'-脱氧胞苷(5-AZA)处理可恢复HCC细胞系中的GATA4和GATA5表达。此外,观察到GATA5前列腺素的甲基化与表现出HCC的患者年龄有关。 GATA4和GATA5表达的恢复在体外抑制了HCC细胞的集落形成并诱导了其凋亡。本研究得出结论,肝癌组织和细胞系中GATA4和GATA5的表达水平降低。 5-AZA处理可恢复HCC细胞系中的GATA4和GATA5表达,抑制肿瘤细胞的生长和集落形成,并诱导细胞凋亡。

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