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短时间孵育时的细胞毒性活性分析揭示了线粒体复合物 I 抑制剂番荔枝烷型二萜的显著差异。

Analysis of cytotoxic activity at short incubation times reveals profound differences among Annonaceus acetogenins, inhibitors of mitochondrial Complex I.

机构信息

Fundación MEDINA. Parque Tecnológico Ciencias de la Salud, Avenida del Conocimiento 3, 18100 Granada, Spain.

出版信息

J Bioenerg Biomembr. 2013 Feb;45(1-2):145-52. doi: 10.1007/s10863-012-9490-8. Epub 2012 Nov 21.

Abstract

Annonaceous acetogenins are potent cytotoxic agents against tumor cell lines as well as potent inhibitors of mitochondrial Complex I (Degli Esposti and Ghelli Biochim Biophys Acta 1187:116-120, 1994; Degli Esposti et al. Biochem J 301(Pt 1):161-167, 1994; Tormo et al. Arch Biochem Biophys 369:119-126, 1999). Eighteen different ACGs belonging to seven structural sub-families were tested against six tumor and two non tumor cell lines in a MTT cytotoxicity assay to evaluate the correlation between mitochondrial Complex I inhibition and cytotoxic activity potency and selectivity. The results showed a substantial heterogeneity in potency and selectivity among the different compounds tested, although no clear overall structure-activity relationships could be established. To further characterize the biological activity of these compounds, four ACGs were selected based on their inhibition binding sites to Complex I, to evaluate their cytotoxic activity over a 15-minute to 48-hour period using a more sensitive time-course LDH cytotoxicity assay. Our results indicate that, although all of the ACGs were highly cytotoxic in HepG2 cell lines at 24 h, each sub-class behaves rather differently at shorter times. Perhaps other aspects related to how these compounds reach or bind to their target sites, or differences in their ability to cross the cell and/or the mitochondrial membranes, could help explain their different activities. This different behavior between ACGs may provide new clues for a better understanding of their potential antitumor properties.

摘要

番荔枝乙酰二萜类化合物是针对肿瘤细胞系的有效细胞毒性剂,也是线粒体复合物 I 的有效抑制剂(DegliEsposti 和 Ghelli Biochim Biophys Acta 1187:116-120, 1994;DegliEsposti 等人。 Biochem J 301(Pt 1):161-167, 1994;Tormo 等人。 Arch Biochem Biophys 369:119-126, 1999)。在 MTT 细胞毒性测定中,对 6 种肿瘤细胞系和 2 种非肿瘤细胞系进行了 18 种不同的 ACG (属于 7 种结构亚家族)的测试,以评估线粒体复合物 I 抑制与细胞毒性活性强度和选择性之间的相关性。结果表明,尽管在所测试的不同化合物之间存在明显的异质性,但无法建立明确的整体结构-活性关系。为了进一步表征这些化合物的生物学活性,根据它们对复合物 I 的抑制结合位点,选择了 4 种 ACG,以评估它们在更敏感的时间过程 LDH 细胞毒性测定中在 15 分钟至 48 小时期间的细胞毒性活性。我们的结果表明,尽管所有的 ACG 在 HepG2 细胞系中在 24 小时时均具有高细胞毒性,但在较短时间内,每个亚类的行为却大不相同。也许与这些化合物如何到达或与其靶标结合相关的其他方面,或者它们穿过细胞和/或线粒体膜的能力的差异,可以帮助解释它们的不同活性。ACG 之间的这种不同行为可能为更好地理解其潜在的抗肿瘤特性提供新的线索。

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