Pharmacognosy Research Laboratories, Medway School of Science, University of Greenwich, Chatham-Maritime, Kent ME4 4TB, UK.
Fitoterapia. 2010 Dec;81(8):1013-9. doi: 10.1016/j.fitote.2010.06.021. Epub 2010 Jul 1.
The present study examines the comparative cytotoxicity of knipholone (KP) and knipholone anthrone (KA) in leukaemic and melonocyte cancer cell lines. It was found that KA induces a rapid onset of cytotoxicity with IC(50) values ranging from 0.5 to 3.3 μM. In comparison to KA, KP was 70-480-times less toxic to cancer cells. Morphological and biochemical studies revealed that the cytotoxicity of KA was coupled with a quick loss of membrane integrity leading to necrotic cell death. The study identified KA as a new class of natural potential anticancer agent with a wide range of toxicological and pharmacological implications.
本研究考察了 knipholone (KP) 和 knipholone 蒽酮 (KA) 在白血病和黑素瘤癌细胞系中的比较细胞毒性。结果发现,KA 诱导细胞毒性的快速发生,IC50 值范围为 0.5 至 3.3 μM。与 KA 相比,KP 对癌细胞的毒性低 70-480 倍。形态学和生化研究表明,KA 的细胞毒性与细胞膜完整性的迅速丧失有关,导致坏死性细胞死亡。该研究确定 KA 为一种新型天然潜在抗癌剂,具有广泛的毒理学和药理学意义。