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Isoliquiritigenin-Induced Differentiation in Mouse Melanoma B16F0 Cell Line

机译:异黄体生成素诱导的小鼠黑色素瘤B16F0细胞系分化

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The chemotherapeutical treatment is very limited for malignant melanoma, a highly lethal disease occurs globally. Natural products derived from traditional Chinese medicine licorice are attractive in quest new treatments due to their anti-tumor activities. A new dietary flavonoid isoliquiritigenin (ISL) were thus investigated to indentify its anti-melanoma activities on mouse melanoma B16F0 cells in present study. Using biochemical and free radical biological experiments in vitro, we identified the pro-differentiated profiles of ISL and evaluated the role of reactive oxygen species (ROS) during B16F0 cell differentiation. The data showed a strong dose-response relationship between ISL exposure and the characteristics of B16F0 differentiation in terms of morphology changes and melanogenesis. The accumulated intercellular ROS during exposure are necessary to support ISL-induced differentiation, which was proven by additional redox modulators. It was confirmed further by the relative activities of enzymes and genes modulated melanogenesis in ISL-treatments with or without ROS modulators. The tumorigenicity of ISL-treated cells was limited significantly by using the colony formation assay in vitro and an animal model assay in vivo respectively. Our research demonstrated that isoliquiritigenin is a differentiation-inducing agent, and its mechanisms involve ROS accumulation facilitating melanogenesis.
机译:恶性黑色素瘤的化学治疗方法非常有限,全球普遍存在高度致死性疾病。源自中药甘草的天然产物由于其抗肿瘤活性而在寻求新疗法方面具有吸引力。因此,在本研究中,研究了一种新的饮食类黄酮异黄体生成素(ISL),以确定其对小鼠黑素瘤B16F0细胞的抗黑素瘤活性。使用体外的生化和自由基生物学实验,我们鉴定了ISL的促分化谱,并评估了B16F0细胞分化过程中活性氧(ROS)的作用。数据显示,在形态变化和黑色素生成方面,ISL暴露与B16F0分化特征之间存在很强的剂量反应关系。暴露过程中积累的细胞间ROS对于支持ISL诱导的分化是必需的,这已被其他氧化还原调节剂证实。在有或没有ROS调节剂的ISL治疗中,酶和基因调节的黑色素生成的相对活性进一步证实了这一点。分别通过体外集落形成测定和体内动物模型测定,ISL处理的细胞的致瘤性受到显着限制。我们的研究表明,异寡糖原蛋白是一种分化诱导剂,其机制涉及ROS积累,促进黑色素生成。

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