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

被引:263
作者
Houghton, Peter [1 ]
Fang, Rui [1 ]
Techatanawat, Isariya [1 ]
Steventon, Glyn [1 ]
Hylands, Peter J. [1 ]
Lee, C. C. [1 ]
机构
[1] Kings Coll London, Pharmaceut Sci Res Div, London SE1 9NN, England
关键词
cytotoxicity testing; SRB assay; antioxidant; GST upregulation; phenylpropanoids; flavonoids; alpinia;
D O I
10.1016/j.ymeth.2007.01.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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-trans fe rase (GST) activity in cultured hepatocytes and this was traced to the phenylpropanoids present, especially V-acetoxychavicol acetate. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:377 / 387
页数:11
相关论文
共 29 条
[1]  
Bae EA, 1999, BIOL PHARM BULL, V22, P1314, DOI 10.1248/bpb.22.1314
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]  
CHANG TKH, 1993, CANCER RES, V53, P5629
[4]  
COLE SPC, 1986, CANCER CHEMOTH PHARM, V17, P259
[5]   Cytotoxicity and lipid peroxidation-inhibiting activity of flavonoids [J].
Cos, P ;
Calomme, M ;
Sindambiwe, JB ;
De Bruyne, T ;
Cimanga, K ;
Pieters, L ;
Vlietinck, AJ ;
Vanden Berghe, D .
PLANTA MEDICA, 2001, 67 (06) :515-519
[6]   Comparative study of eight well-known polyphenolic antioxidants [J].
Cos, P ;
Hermans, N ;
Calomme, M ;
Maes, L ;
De Bruyne, T ;
Pieters, L ;
Viletinck, AJ ;
Vanden Berghe, D .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2003, 55 (09) :1291-1297
[7]   In vitro antioxidant profile of phenolic acid derivatives [J].
Cos, P ;
Rajan, P ;
Vedernikova, I ;
Calomme, M ;
Pieters, L ;
Vlietinck, AJ ;
Augustyns, K ;
Haemers, A ;
Vanden Berghe, D .
FREE RADICAL RESEARCH, 2002, 36 (06) :711-716
[8]  
Cos P, 2001, FREE RADICAL BIO MED, V31, pS30
[9]  
da Rocha Adriana B., 2001, Current Opinion in Pharmacology, V1, P364
[10]  
DANIELS LB, 1981, J BIOL CHEM, V256, P3004