Anticancer potential of Amaryllidaceae alkaloids evaluated by screening with a panel of human cells, real-time cellular analysis and Ehrlich tumor-bearing mice
Language English Country Ireland Media print-electronic
Document type Journal Article
PubMed
28756149
DOI
10.1016/j.cbi.2017.07.018
PII: S0009-2797(17)30671-3
Knihovny.cz E-resources
- Keywords
- Alkaloids, Amaryllidaceae, Antiproliferative activity, In vitro, In vivo,
- MeSH
- Alkaloids chemistry pharmacology therapeutic use MeSH
- Amaryllidaceae chemistry metabolism MeSH
- Apoptosis drug effects MeSH
- Carcinoma, Ehrlich Tumor drug therapy mortality pathology MeSH
- Antineoplastic Agents, Phytogenic chemistry pharmacology therapeutic use MeSH
- Kaplan-Meier Estimate MeSH
- Humans MeSH
- Mice MeSH
- Cell Line, Tumor MeSH
- Cell Proliferation drug effects MeSH
- Drug Screening Assays, Antitumor MeSH
- Transplantation, Heterologous MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Alkaloids MeSH
- Antineoplastic Agents, Phytogenic MeSH
In this study, twenty-two Amaryllidaceae alkaloids were screened for their anticancer potential. All isolates were evaluated for antiproliferative activities on a panel of 17 human cell types of different tissue origin using WST-1 assay. In addition, we determined the antiproliferative effect with a real-time cell analysis xCELLigence system. Thereafter, to evaluate the barely known in vivo anticancer potential of the most potent molecule haemanthamine, a preliminary study was performed using an Ehrlich tumor-bearing mice model. The results showed that haemanthamine, lycorine and haemanthidine exerted the highest antiproliferative activity. The mean growth percent (GP) value after a single-dose 10 μM treatment was for haemanthamine 21%, for lycorine 21% and for haemanthidine 27% that of untreated control cells (100%). Furthermore, haemanthamine, lycorine and haemanthidine exhibited significant cytotoxicities against all the tested cell lines with individual IC50 values in the micromolar range. Dynamic real-time measures of impedance by xCELLigence indicated that these three compounds suppress cell proliferation after 10 h of treatment at a concentration of 10 μM or higher. Regrettably, in a follow-up in vivo antitumor activity study, haemanthamine showed no statistically significant reduction in the tumor size with no prolongation of survival time of Ehrlich tumor-bearing mice. Taken together, these results provide a new clue and guidance for exploiting Amaryllidaceae alkaloids as anticancer agents.
References provided by Crossref.org
Undescribed Amaryllidaceae Alkaloids from Zephyranthes citrina and Their Cytotoxicity
Chemistry and Biological Activity of Alkaloids from the Genus Lycoris (Amaryllidaceae)
The Genus Nerine Herb. (Amaryllidaceae): Ethnobotany, Phytochemistry, and Biological Activity