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Cell cycle arrest through inhibition of tubulin polymerization by withaphysalin F,a bioactive compound isolated from Acnistus arborescens
Authors:Danilo D. Rocha  Aruna Balgi  Ana Isabel V. Maia  Otilia D. Pessoa  Edilberto R. Silveira  Letícia V. Costa-Lotufo  Michel Roberge  Claudia Pessoa
Affiliation:1.Laboratório de Oncologia Experimental, Departamento de Fisiologia e Farmacologia,Universidade Federal do Ceará,Fortaleza,Brazil;2.Departamento de Química Organica e Inorganica,Universidade Federal do Ceará,Fortaleza,Brazil;3.Department of Biochemistry and Molecular Biology,University of British Columbia,Vancouver,Canada
Abstract:Many compounds used in the treatment of cancer possess tubulin-interacting properties that lead to mitotic arrest. Withaphysalins are potent cytotoxic compounds that are commonly found in plants belonging to the Solanaceae family, such as Acnistus arborescens; however, the cytotoxic mechanisms or molecular targets of these compounds remain unknown. Thus, the aim of this study was to evaluate the effects of whitaphysalins on cancer cell cycle progression and tubulin interaction. In this report, we show the antiproliferative activity of withaphysalin F and its effect in arresting cells in the G2/M phase of the cell cycle. These two effects are the result of the interference of withaphysalin F in the polymerization of microtubules. Withaphysalin F also induced DNA fragmentation, which can be related to an increase in mitochondrial membrane depolarization. These results suggest that interference of withaphysalin F in microtubule polymerization may induce cell cycle arrest in the G2/M phase and therefore contribute to growth inhibition of tumor cells in vitro. Taken together, these studies indicate that withaphysalin F could potentially be used as an anticancer drug.
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