Affiliation:
1. Institute of Pharmacology and Toxicology, University of Würzburg, Versbacher Str. 9, 97078 Würzburg, Germany
2. Institute of Chemistry, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, CauGiay, Hanoi, Vietnam
Abstract
Background: Vinca alkaloids are important cancer drugs belonging to the class of antimitotic
agents. The most commonly used substances are vinblastine and vincristine, other compounds
are vinorelbine and vinflunine. All of them are very effective drugs but their use is limited by severe
side-effects including neurotoxicity and bone marrow depression. Therefore, it is very important to
develop novel vinca alkaloids with similar efficacy but lower toxicity.
</P><P>
Methods: Here, we analyzed two new compounds, 4-chlorochablastine and 4-chlorochacristine, with
regard to their biological activity. These novel compounds were applied to a leukemia cell line at
clinically relevant concentrations. For comparison, the established vinca alkaloids vinblastine, vincristine,
vinorelbine, and vinflunine were also tested.
</P><P>
Results: Both novel substances decreased cellular proliferation. Apoptosis was found to be increased
using two different methods reflecting early and late apoptosis. Cell cycle analysis revealed a clear
decrease in G1-cells and an increase in G2/M-cells indicating an arrest in mitosis. In general, 4-
chlorochablastine and 4-chlorochacristine caused these effects at concentrations higher than those
needed for vinblastine, vincristine, and vinorelbine, but the potency was approximately in the range
of vinflunine.
</P><P>
Conclusion: Taken together, the results show first indications that these novel vinca alkaloids might
be effective and that they warrant further analysis.
Publisher
Bentham Science Publishers Ltd.
Subject
Cancer Research,Drug Discovery,Pharmacology,Oncology
Reference25 articles.
1. Go R, Yien CY, Nazre M. Vinca alkaloids.
2. Beer CT, Cutts JH. Role of chance observations in chemotherapy: Vinca rosea.
3. Harrison D, Timasheff SN. Interaction of vinblastine with calf brain microtubule protein.
4. Wang C, Ravelli RB, Roussi F, Steinmetz MO, Curmi PA, Sobel A, Knossow M. Structural basis for the regulation of tubulin by vinblastine.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献