首页> 外文期刊>Journal of cellular biochemistry. >Regulatory effect of resveratrol and prednisolone on MDR1 MDR1 gene expression in acute lymphoblastic leukemia cell line (CCRF‐CEM): An epigenetic perspective
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Regulatory effect of resveratrol and prednisolone on MDR1 MDR1 gene expression in acute lymphoblastic leukemia cell line (CCRF‐CEM): An epigenetic perspective

机译:白藜芦醇和泼尼松龙对急性淋巴细胞白血病细胞MDR1MDR1基因表达的调节作用(CCRF-CEM):表观遗传观点

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Abstract Chemotherapy is the most common method to treat leukemia as well as other types of human cancers. However, drug resistance has remained as the main challenge against the efficacy of treatments. Furthermore, having various adverse effects, chemotherapy drugs are becoming replaced by natural modalities for cancer therapy. In this regard, herbal components such as resveratrol and prednisolone have been identified to sensitize the leukemic cells to programmed cell death through a set of complex processes. In this study, we have examined DNA methylation on the human multidrug resistance gene 1 ( MDR1 ) as a well‐known marker for cellular drug resistance. We evaluated the effect of resveratrol and prednisolone on DNA methylation patterns of MDR1 gene promoter in the CCRF‐CEM cell line as a representative for acute lymphoblastic leukemia. The study was aimed to clarify whether the MDR1 gene expression is regulated via DNA promoter methylation as a potential underlying mechanism, following exposure to resveratrol and prednisolone. Our data revealed that despite a strong influence to down‐regulate the MDR1 expression, Resveratrol and Prednisolone did not alter the methylation pattern, suggesting other regulatory mechanisms in controlling the MDR1 expression in CCRF‐CEM cell line. Unchanged status of DNA methylation of MDR1 gene may suggest that Resveratrol and Prednisolone causes the gene expression changes through a distinct mechanism which requires further studies to be understood. A more detailed understanding of the mechanisms beyond the regulation of the genes involved in cancer formation will help to design novel therapeutic strategies to fight the human cancers.
机译:摘要化疗是治疗白血病以及其他类型的人类癌症的最常见方法。然而,耐药物仍然是对治疗效果的主要挑战。此外,具有各种不利影响,化疗药物被癌症治疗的天然型号取代。在这方面,已经鉴定了诸如白藜芦醇和泼尼松龙的草药组分以使白血病细胞敏化通过一组复杂的方法对细胞死亡进行编程。在该研究中,我们在人类多药抗性基因1(MDR1)上检测了DNA甲基化作为用于细胞耐药性的公知标记。我们评估了白藜芦醇和泼尼松龙对CCRF-CEM细胞系MDR1基因启动子DNA甲基化模式的影响,作为急性淋巴细胞白血病的代表性。该研究旨在阐明MDR1基因表达是否通过DNA启动子甲基化作为潜在的基础机制来调节,暴露于白藜芦醇和泼尼松酮之后。我们的数据显示,尽管对MDR1表达的强烈影响较大,但白藜芦醇和泼尼松龙并未改变甲基化模式,表明在CCRF-CEM细胞系中控制MDR1表达的其他调节机制。 MDR1基因的DNA甲基化的不变状态可能表明,白藜芦醇和泼尼松龙通过截然不同的机制导致基因表达改变,这需要改进研究。更详细地了解超出参与癌症形成的基因的机制将有助于设计对抗人类癌症的新的治疗策略。

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