Abstract | BACKGROUND AND PURPOSE:
Andrographolide, the major phytoconstituent of Andrographis paniculata, was previously shown by us to have activity against breast cancer. This led to synthesis of new andrographolide analogues to find compounds with better activity than the parent compound. Selected benzylidene derivatives were investigated for their mechanisms of action by studying their effects on the cell cycle progression and cell death. EXPERIMENTAL APPROACH: Microculture tetrazolium, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) and sulphorhodamine B (SRB) assays were utilized in assessing the in vitro growth inhibition and cytotoxicity of compounds. Flow cytometry was used to analyse the cell cycle distribution of control and treated cells. CDK1 and CDK4 levels were determined by western blotting. Apoptotic cell death was assessed by fluorescence microscopy and flow cytometry. KEY RESULTS: Compounds, in nanomolar to micromolar concentrations, exhibited growth inhibition and cytotoxicity in MCF-7 (breast) and HCT-116 ( colon) cancer cells. In the NCI screen, 3,19-(2-bromobenzylidene) andrographolide (SRJ09) and 3,19-(3-chloro-4-fluorobenzylidene) andrographolide (SRJ23) showed greater cytotoxic potency and selectivity than andrographolide. SRJ09 and SRJ23 induced G(1) arrest and apoptosis in MCF-7 and HCT-116 cells, respectively. SRJ09 downregulated CDK4 but not CDK1 level in MCF-7 cells. Apoptosis induced by SRJ09 and SRJ23 in HCT-116 cells was confirmed by annexin V-FITC/PI flow cytometry analysis. CONCLUSION AND IMPLICATIONS:
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Authors | S R Jada, C Matthews, M S Saad, A S Hamzah, N H Lajis, M F G Stevens, J Stanslas |
Journal | British journal of pharmacology
(Br J Pharmacol)
Vol. 155
Issue 5
Pg. 641-54
(Nov 2008)
ISSN: 1476-5381 [Electronic] England |
PMID | 18806812
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- 3,19-(2-bromobenzylidene)andrographolide
- Antineoplastic Agents
- Benzylidene Compounds
- Diterpenes
- andrographolide
- CDC2 Protein Kinase
- Cyclin-Dependent Kinase 4
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Topics |
- Antineoplastic Agents
(chemical synthesis, chemistry, pharmacology)
- Apoptosis
(drug effects)
- Benzylidene Compounds
(chemical synthesis, chemistry, pharmacology)
- Blotting, Western
- Breast Neoplasms
(drug therapy, enzymology, pathology)
- CDC2 Protein Kinase
(biosynthesis)
- Cell Line, Tumor
- Cell Survival
(drug effects)
- Colonic Neoplasms
(drug therapy, enzymology, pathology)
- Cyclin-Dependent Kinase 4
(biosynthesis)
- Diterpenes
(chemical synthesis, chemistry, pharmacokinetics)
- Dose-Response Relationship, Drug
- Flow Cytometry
- G1 Phase
(drug effects)
- Humans
- Molecular Structure
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