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磺罗丹明(SRB)测定法以及其他用于检测植物提取物和衍生化合物与所谓抗癌活性相关活性的方法。

The sulphorhodamine (SRB) assay and other approaches to testing plant extracts and derived compounds for activities related to reputed anticancer activity.

作者信息

Houghton Peter, Fang Rui, Techatanawat Isariya, Steventon Glyn, Hylands Peter J, Lee C C

机构信息

Pharmaceutical Sciences Research Division, King's College London, Franklin-Wilkins Building 150 Stamford Street, London SE1 9NN, UK.

出版信息

Methods. 2007 Aug;42(4):377-87. doi: 10.1016/j.ymeth.2007.01.003.

Abstract

Since the major approach in searching for potential anticancer agents over the last 50 years has been based on selective cytotoxic effects on mammalian cancer cell lines, cell-based methods for cytotoxicity are described and compared. The sulphorhodamine B (SRB) assay is described in detail as the preferred method and also a novel approach has been developed which is based on the hypothesis that, in some circumstances, the naturally occurring compounds act as prodrugs rather than active compounds in their own right. Consequently, extracts or compounds are pre-incubated with systems modelling metabolic processes in the body before being tested. The methods have been validated using known compounds and Iris tectorum extracts have been shown to be more cytotoxic after treatment with beta-glucosidase. In addition bioassays based on mammalian cells involving antioxidant and upregulation of some cellular self-defence mechanisms are discussed which are related to prevention as well as treatment of cancer. Extracts of Alpinia officinarum induced glutathione-S-transferase (GST) activity in cultured hepatocytes and this was traced to the phenylpropanoids present, especially 1'-acetoxychavicol acetate.

摘要

在过去50年里,寻找潜在抗癌药物的主要方法是基于对哺乳动物癌细胞系的选择性细胞毒性作用,因此本文对基于细胞的细胞毒性检测方法进行了描述和比较。详细介绍了磺酰罗丹明B(SRB)检测法作为首选方法,并且还开发了一种新方法,该方法基于这样的假设:在某些情况下,天然存在的化合物本身作为前药而非活性化合物起作用。因此,提取物或化合物在测试前先与模拟体内代谢过程的系统进行预孵育。这些方法已通过已知化合物进行了验证,鸢尾提取物经β-葡萄糖苷酶处理后显示出更强的细胞毒性。此外,还讨论了基于哺乳动物细胞的生物测定法,这些方法涉及抗氧化剂以及一些细胞自我防御机制的上调,它们与癌症的预防和治疗都有关。高良姜提取物在培养的肝细胞中诱导谷胱甘肽-S-转移酶(GST)活性,这可追溯到其中存在的苯丙素类化合物,尤其是乙酸1'-乙酰氧基查维醇。

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