The effect of Amaryllidaceae alkaloids haemanthamine and haemanthidine on cell cycle progression and apoptosis in p53-negative human leukemic Jurkat cells
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24182986
DOI
10.1016/j.phymed.2013.09.005
PII: S0944-7113(13)00362-0
Knihovny.cz E-resources
- Keywords
- Apoptosis, Caspases, Cell cycle, Haemanthamine, Haemanthidine, Jurkat,
- MeSH
- Amaryllidaceae Alkaloids pharmacology therapeutic use MeSH
- Antineoplastic Agents, Phytogenic analysis MeSH
- Apoptosis drug effects MeSH
- Checkpoint Kinase 1 MeSH
- Phenanthridines pharmacology therapeutic use MeSH
- Phytotherapy * MeSH
- Genes, p53 MeSH
- Cyclin-Dependent Kinase Inhibitor p16 metabolism MeSH
- Jurkat Cells MeSH
- Caspases metabolism MeSH
- Cell Cycle Checkpoints drug effects MeSH
- Drug Screening Assays, Antitumor MeSH
- Leukemia drug therapy MeSH
- Humans MeSH
- Liliaceae chemistry MeSH
- Membrane Potential, Mitochondrial drug effects MeSH
- Protein Kinases metabolism MeSH
- Plant Extracts pharmacology therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Amaryllidaceae Alkaloids MeSH
- Antineoplastic Agents, Phytogenic MeSH
- Checkpoint Kinase 1 MeSH
- CHEK1 protein, human MeSH Browser
- Phenanthridines MeSH
- hemanthamine MeSH Browser
- hemanthidine MeSH Browser
- Cyclin-Dependent Kinase Inhibitor p16 MeSH
- Caspases MeSH
- Protein Kinases MeSH
- Plant Extracts MeSH
Plants from the Amaryllidaceae family have been shown to be a promising source of biologically active natural compounds of which some selected are currently in pre-clinical development. Regardless of interesting pioneer works, little is known about Amaryllidaceae alkaloids that have shown promising anti-cancer activities. The crinane group of the Amaryllidaceae, including haemanthamine and haemanthidine, was amongst the first of these compounds to exhibit an interesting cytotoxic potential against cancer cell lines. However, the mechanism of cytotoxic and anti-proliferative activity is not yet entirely clear. The primary objectives of the current study were to investigate the effects of haemanthamine and haemanthidine on the induction of apoptosis and the cell cycle regulatory pathway in p53-null Jurkat cells. Results indicate that haemanthamine and haemanthidine treatment decreases cell viability and mitochondrial membrane potential, leads to a decline in the percentage of cells in the S phase of the cell cycle, induces apoptosis detected by Annexin V staining and increases caspase activity. Dose dependent apoptosis was cross verified by fluorescence and bright field microscopy through Annexin V/propidium iodine staining and morphological changes which characteristically attend programmed cell death. The apoptotic effect of haemanthamine and haemanthidine on leukemia cells is more pronounced than that of gamma radiation. Contrary to gamma radiation, Jurkat cells do not completely halt the cell cycle 24h upon haemanthamine and haemanthidine exposure. Both Amaryllidaceae alkaloids accumulate cells preferentially at G1 and G2 stages of the cell cycle with increased p16 expression and Chk1 Ser345 phosphorylation. Concerning the pro-apoptotic effect, haemanthidine was more active than haemanthamine in the Jurkat leukemia cell line.
References provided by Crossref.org
Undescribed Amaryllidaceae Alkaloids from Zephyranthes citrina and Their Cytotoxicity
The Genus Nerine Herb. (Amaryllidaceae): Ethnobotany, Phytochemistry, and Biological Activity