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Taccalonolide microtubule stabilizers
Institution:1. Department of Pharmacology, University of Texas Health Science Center at San Antonio, TX 78229, United States;2. Department of Medicine, University of Texas Health Science Center at San Antonio, TX 78229, United States;3. Cancer Therapy & Research Center, University of Texas Health Science Center at San Antonio, TX 78229, United States;1. Inst. of Pharmaceutical Sciences, Eidgenössische Technische Hochschule (ETH) Zürich, Wolfgang-Pauli Strasse 10, Zürich, CH-8093, Switzerland;1. Department of Physiology, Faculty of Medicine, University of Tokat Gaziosmanpasa, Tokat, Turkey;2. Department of Physiology, Faculty of Medicine, University of Ondokuz Mayis, Samsun, Turkey;1. Charles University in Prague, First Faculty of Medicine, Salmovská 1, 120 00 Prague 2, Czech Republic;2. Hospital Na Bulovce, Department of Radiological Physics, Budinova 2, 180 81 Prague 8, Czech Republic;3. Institute of Experimental and Applied Physics, Czech Technical University in Prague, Horska 3a/22, 128 00 Prague 2, Czech Republic;4. Faculty of Science, University of South Bohemia, Branisovska 31, 370 05 Ceske Budejovice, Czech Republic;5. Biology Centre, AS CR, Institute of Entomology, Department of Biochemistry and Physiology, Branisovska 31, CZ-37005 Ceske Budejovice, Czech Republic;1. Center for Neurodegenerative Disease Research, Perelman School of Medicine, University of Pennsylvania, 3600 Spruce Street, Maloney 3, Philadelphia, PA 19104-6323, USA;2. Department of Chemistry, School of Arts and Sciences, University of Pennsylvania, 231 South 34th Street, Philadelphia, PA 19104-6323, USA;1. Facultad de Química, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510 México, D.F., Mexico;2. Departamento de Química de Radiaciones y Radioquímica, Instituto de Ciencias Nucleares, Universidad Nacional Autónoma de México, 04510 México, D.F., Mexico
Abstract:This review focuses on a relatively new class of microtubule stabilizers, the taccalonolides. The taccalonolides are highly oxygenated pentacyclic steroids isolated from plants of the genus Tacca. Originally identified in a cell-based phenotypic screen, the taccalonolides have many properties similar to other microtubule stabilizers. They increase the density of interphase microtubules, causing microtubule bundling, and form abnormal multi-polar mitotic spindles leading to mitotic arrest and, ultimately, apoptosis. However, the taccalonolides differ from other microtubule stabilizers in that they retain efficacy in taxane resistant cell lines and in vivo models. Binding studies with the newly identified, potent taccalonolide AJ demonstrated covalent binding to β-tubulin at or near the luminal and/or pore taxane binding site(s) which stabilizes microtubule protofilaments in a unique manner as compared to other microtubule stabilizers. The isolation and semi-synthesis of 21 taccalonolides helped to identify key structure activity relationships and the importance of multiple regions across the taccalonolide skeleton for optimal biological potency.
Keywords:Tacca  Taccalonolide  Microtubule  Tubulin  Microtubule stabilizer  Taxol  Paclitaxel  Laulimalide
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