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Epigenetic reactivation of RANK in glioblastoma cells by curcumin: involvement of STAT3 inhibition.

机译:姜黄素对胶质母细胞瘤细胞中RANK的表观遗传激活:STAT3抑制作用。

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摘要

DNA methylation plays an essential role in carcinogenesis. Promoter hypermethylation can result in transcriptional silencing of specific genes, such as tumor suppressors. Thus far, few reports have investigated the effect of curcumin, an active component of the perennial herb Curcuma longa, on DNA methylation. In the present study, we evaluated the effects of curcumin on receptor activator of NF- kappa B (RANK) gene expression in human glioblastoma cells. Incubation of cells with therapeutic concentrations of curcumin resulted in a significant elevation of RANK expression at both the mRNA and protein levels in two glioblastoma cell lines. We further confirmed that this elevation was associated with promoter demethylation through methylation-specific polymerase chain reaction (PCR) and bisulfite sequencing PCR. Additionally, we demonstrated that knockdown of STAT3, an oncogenic transcription factor, is sufficient to induce RANK promoter demethylation along with RANK reactivation. These results demonstrated that curcumin induced RANK gene reactivation through epigenetic modification in human glioblastoma cells, and that STAT3 is involved in RANK promoter hypermethylation and epigenetic silencing, thus allowing for further applications of curcumin epigenetic therapy in glioma and therapeutic implications of STAT3 in human glioblastoma.
机译:DNA甲基化在致癌过程中起着至关重要的作用。启动子高甲基化可导致特定基因的转录沉默,例如肿瘤抑制子。迄今为止,很少有报道研究多年生草本姜黄的活性成分姜黄素对DNA甲基化的影响。在本研究中,我们评估了姜黄素对人胶质母细胞瘤细胞中NF-κB(RANK)基因表达受体激活剂的影响。用治疗浓度的姜黄素温育细胞会导致两种胶质母细胞瘤细胞系的mRNA和蛋白水平的RANK表达显着升高。我们进一步证实,这种升高与通过甲基化特异性聚合酶链反应(PCR)和亚硫酸氢盐测序PCR的启动子去甲基化有关。此外,我们证明了,STAT3(一种致癌转录因子)的敲低足以诱导RANK启动子去甲基化以及RANK重新激活。这些结果表明姜黄素通过人胶质母细胞瘤细胞中的表观遗传修饰诱导RANK基因重新激活,并且STAT3参与RANK启动子的超甲基化和表观遗传沉默,从而允许姜黄素表观遗传疗法在神经胶质瘤中的进一步应用以及STAT3在人胶质母细胞瘤中的治疗意义。

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