首页> 美国卫生研究院文献>International Journal of Molecular Sciences >A Novel Naphthyridine Derivative 3u Induces Necroptosis at Low Concentrations and Apoptosis at High Concentrations in Human Melanoma A375 Cells
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A Novel Naphthyridine Derivative 3u Induces Necroptosis at Low Concentrations and Apoptosis at High Concentrations in Human Melanoma A375 Cells

机译:新型萘啶衍生物3u在人黑素瘤A375细胞中低浓度诱导坏死性坏死高浓度诱导凋亡。

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摘要

Naphthyridine derivatives are a widely-used class of heterocycles due to their pharmacological activities. A novel compound (10-Methoxy-1,2,3,4-tetrahydrobenzo(g)(1,3) diazepino(1,2-a)-(1,8)naphthyridin-6-yl)(phenyl) methanone (named 3u), showed good anticancer activity in the human malignant melanoma cell line A375 via Thiazolyl Blue Tetrazolium Bromide (MTT) assay. After Western blotting confirmed, we found that 3u induces necroptosis at low concentrations and apoptosis at high concentrations via the upregulation of death receptors and scaffold protein in A375 cells. Furthermore, by combining 3u with the caspase inhibitor zVAD-fmk or Receptor Interacting Serine/Threonine Kinase 1 (RIP1) kinase inhibitor Necrostatin-1 (Nec-1), we found that the activity of caspase-8 was the crucial factor that determined whether either apoptosis or necroptosis occurred. The results indicate that 3u should be considered as a potential chemical substance for melanoma treatment.
机译:萘啶衍生物由于其药理活性而被广泛使用。新型化合物(10-甲氧基-1,2,3,4-四氢苯并(g)(1,3)二氮杂环庚烷(1,2-a)-(1,8)萘啶-6-基)(苯基)甲酮(命名为3u),通过噻唑基溴化四氮唑蓝(MTT)分析在人类恶性黑色素瘤细胞系A375中显示出良好的抗癌活性。 Western印迹证实后,我们发现3u通过上调A375细胞中的死亡受体和支架蛋白来诱导坏死性坏死和高浓度诱导凋亡。此外,通过将3u与半胱天冬酶抑制剂zVAD-fmk或受体相互作用的丝氨酸/苏氨酸激酶1(RIP1)激酶抑制剂Necrostatin-1(Nec-1)结合,我们发现caspase-8的活性是决定是否发生凋亡或坏死。结果表明3u应该被认为是治疗黑色素瘤的潜在化学物质。

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