Photopharmacology of Antimitotic Agents |
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Authors: | Susanne Kirchner Zbigniew Pianowski |
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Affiliation: | 1.Institute of Organic Chemistry, Karlsruhe Institute of Technology, 76131 Karlsruhe, Germany;2.Institute of Biological and Chemical Systems–FMS, Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen, Germany |
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Abstract: | Antimitotic agents such as the clinically approved vinca alkaloids, taxanes and epothilone can arrest cell growth during interphase and are therefore among the most important drugs available for treating cancer. These agents suppress microtubule dynamics and thus interfere with intracellular transport, inhibit cell proliferation and promote cell death. Because these drugs target biological processes that are essential to all cells, they face an additional challenge when compared to most other drug classes. General toxicity can limit the applicable dose and therefore reduce therapeutic benefits. Photopharmacology aims to avoid these side-effects by introducing compounds that can be applied globally to cells in their inactive form, then be selectively induced to bioactivity in targeted cells or tissue during a defined time window. This review discusses photoswitchable analogues of antimitotic agents that have been developed by combining different photoswitchable motifs with microtubule-stabilizing or microtubule-destabilizing agents. |
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Keywords: | photopharmacology microtubule-targeting agents antimitotic agents molecular photoswitches |
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