Abstract
We discovered a thalidomide analogue [5-hydroxy-(2,6-diisopropylphenyl)-1H-isoindole-1,3-dione (5HPP-33)] with antiproliferative activity against nine cancer cell lines in vitro. Flow cytometric analyses showed that the compound caused G2-M arrest, which occurred mainly at the mitotic phase. In addition, immunofluorescence microscopy and in vitro tubulin polymerization studies showed that 5HPP-33 has antimicrotubule activity with a paclitaxel-like mode of action. It is effective against four different paclitaxel-resistant cell lines. Thus, 5HPP-33 represents a potential antitumor agent. Copyright © 2006 American Association for Cancer Research.
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CITATION STYLE
Li, P. K., Pandit, B., Sackett, D. L., Hu, Z., Zink, J., Zhi, J., … Li, C. (2006). A thalidomide analogue with in vitro antiproliferative, antimitotic, and microtubule-stabilizing activities. Molecular Cancer Therapeutics, 5(2), 450–456. https://doi.org/10.1158/1535-7163.MCT-05-0254
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