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Delphinidin Induces Necrosis in Hepatocellular Carcinoma Ceils in the Presence of 3-Methyladenine, an Autophagy Inhibitor

机译:Delphinidin在自噬抑制剂3-甲基腺嘌呤的存在下诱导肝细胞癌坏死

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摘要

The present study was performed to determine whether anthocyanins could trigger different modes of cell death in different cancers. It was found that whereas cyanidin-3-rutinoside and delphinidin could induce apoptosis in leukemia cells, they caused growth retardation in hepatocellular carcinoma cells (HCC), which was accompanied with a significant cellular vacuolization. The latter was likely caused by macroautophagy and was completely suppressed by 3-methyladenine, ah inhibitor of class III phosphoinositide 3-kinase that is important for autophagy activation, and by bafilomycin A1, which blocks lysosomal degradation. Delphinidin induced significant lipidatioh of LC3, an indication of macroautophagy, which was also suppressed by 3-methyladenine. Macroautophagy was required for the survival of delphinidin-treated HCC cells as inhibition with 3-methyladenine led to massive necrosis without caspase activation. Thus, anthocyanins could induce different modes of cell death for different cancers. Furthermore, anthocyanins could be used in combination with a macroautophagy inhibitor for treating cancers such as HCC.
机译:进行本研究以确定花色苷是否可以在不同的癌症中引发不同的细胞死亡方式。结果发现,虽然花青素-3-芸苔苷和翠雀碱可诱导白血病细胞凋亡,但它们却导致肝细胞癌细胞(HCC)的生长迟缓,并伴有明显的细胞空泡化。后者可能是由于巨噬细胞自噬引起的,并被3-甲基腺嘌呤(一种对自噬激活很重要的III类磷酸肌醇3-激酶抑制剂)和被阻止溶酶体降解的bafilomycin A1完全抑制了。 Delphinidin诱导LC3的显着脂质化,这是大自噬的一种迹象,也被3-甲基腺嘌呤抑制。巨噬细胞自噬是必需的,因为用3-甲基腺嘌呤抑制可导致大量坏死而不激活caspase,因此用delphinidin处理的HCC细胞必须存活。因此,花色苷可以针对不同的癌症诱导不同的细胞死亡方式。此外,花青素可与大自噬抑制剂联合用于治疗癌症,例如HCC。

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