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Echinacoside Induces Apoptosis in Human SW480 Colorectal Cancer Cells by Induction of Oxidative DNA Damages

机译:紫锥菊苷通过诱导氧化性DNA损伤诱导人SW480大肠癌细胞凋亡。

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摘要

Echinacoside is a natural compound with potent reactive oxygen species (ROS)-scavenging and anti-oxidative bioactivities, which protect cells from oxidative damages. As cancer cells are often under intense oxidative stress, we therefore tested if Echinacoside treatment would promote cancer development. Surprisingly, we found that Echinacoside significantly inhibited the growth and proliferation of a panel of cancer cell lines. Treatment of the human SW480 cancer cells with Echinacoside resulted in marked apoptosis and cell cycle arrest, together with a significant increase in active caspase 3 and cleaved PARP, and upregulation of the G1/S-CDK blocker CDKN1B (p21). Interestingly, immunocytochemistry examination of drug-treated cancer cells revealed that Echinacoside caused a significant increase of intracellular oxidized guanine, 8-oxoG, and dramatic upregulation of the double-strand DNA break (DSB)-binding protein 53BP1, suggesting that Echinacoside induced cell cycle arrest and apoptosis in SW480 cancer cells via induction of oxidative DNA damages. These results establish Echinacoside as a novel chemical scaffold for development of anticancer drugs.
机译:紫锥菊苷是一种天然化合物,具有有效的清除活性氧(ROS)和抗氧化的生物活性,可保护细胞免受氧化损伤。由于癌细胞通常处于强烈的氧化应激下,因此我们测试了紫锥菊苷治疗是否会促进癌症的发展。令人惊讶地,我们发现紫锥花苷显着抑制了一组癌细胞系的生长和增殖。用松果菊苷治疗人SW480癌细胞导致明显的凋亡和细胞周期停滞,同时活性胱天蛋白酶3和PARP的裂解显着增加,并且G1 / S-CDK阻断剂CDKN1B上调(p21)。有趣的是,对药物处理过的癌细胞进行免疫细胞化学检查后发现,紫锥花苷引起细胞内氧化鸟嘌呤,8-oxoG的显着增加,以及双链DNA断裂(DSB)结合蛋白53BP1的显着上调,表明紫锥花苷可诱导细胞周期通过诱导DNA氧化损伤阻止SW480癌细胞的凋亡和凋亡。这些结果将紫锥花苷确立为开发抗癌药物的新型化学支架。

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