Anticancer activity of natural cytokinins: a structure-activity relationship study
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20553699
DOI
10.1016/j.phytochem.2010.04.018
PII: S0031-9422(10)00142-1
Knihovny.cz E-resources
- MeSH
- Adenosine analogs & derivatives chemistry pharmacology MeSH
- Cytokinins * analysis chemistry metabolism MeSH
- Genes, p53 drug effects genetics MeSH
- Inhibitory Concentration 50 MeSH
- Isopentenyladenosine analogs & derivatives chemistry pharmacology MeSH
- Kinetin chemistry pharmacology MeSH
- Humans MeSH
- Molecular Structure MeSH
- National Cancer Institute (U.S.) MeSH
- Antineoplastic Agents chemistry pharmacology MeSH
- Plant Growth Regulators pharmacology MeSH
- Drug Screening Assays, Antitumor MeSH
- Stereoisomerism MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- United States MeSH
- Names of Substances
- Adenosine MeSH
- Cytokinins * MeSH
- Isopentenyladenosine MeSH
- kinetin riboside MeSH Browser
- Kinetin MeSH
- N(6)-benzyladenosine MeSH Browser
- Antineoplastic Agents MeSH
- Plant Growth Regulators MeSH
- zeatin riboside MeSH Browser
Cytokinin ribosides (N(6)-substituted adenosine derivatives) have been shown to have anticancer activity both in vitro and in vivo. This study presents the first systematic analysis of the relationship between the chemical structure of cytokinins and their cytotoxic effects against a panel of human cancer cell lines with diverse histopathological origins. The results confirm the cytotoxic activity of N(6)-isopentenyladenosine, kinetin riboside, and N(6)-benzyladenosine and show that the spectrum of cell lines that are sensitive to these compounds and their tissues of origin are wider than previously reported. The first evidence that the hydroxylated aromatic cytokinins (ortho-, meta-, para-topolin riboside) and the isoprenoid cytokinin cis-zeatin riboside have cytotoxic activities is presented. Most cell lines in the panel showed greatest sensitivity to ortho-topolin riboside (IC(50)=0.5-11.6 microM). Cytokinin nucleotides, some synthesized for the first time in this study, were usually active in a similar concentration range to the corresponding ribosides. However, cytokinin free bases, 2-methylthio derivatives and both O- and N-glucosides showed little or no toxicity. Overall the study shows that structural requirements for cytotoxic activity of cytokinins against human cancer cell lines differ from the requirements for their activity in plant bioassays. The potent anticancer activity of ortho-topolin riboside (GI(50)=0.07-84.60 microM, 1st quartile=0.33 microM, median=0.65 microM, 3rd quartile=1.94 microM) was confirmed using NCI(60), a standard panel of 59 cell lines, originating from nine different tissues. Further, the activity pattern of oTR was distinctly different from those of standard anticancer drugs, suggesting that it has a unique mechanism of activity. In comparison with standard drugs, oTR showed exceptional cytotoxic activity against NCI(60) cell lines with a mutated p53 tumour suppressor gene. oTR also exhibited significant anticancer activity against several tumour models in in vivo hollow fibre assays.
References provided by Crossref.org
Cytokinin Plant Hormones Have Neuroprotective Activity in In Vitro Models of Parkinson's Disease