Microtubules are dynamic and structural cellular components involved in several cell functions, including cell shape, motility, and intracellular trafficking. In proliferating cells, they are essential components in the division process through the formation of the mitotic spindle. As a result of these functions, tubulin and microtubules are targets for anticancer agents. Microtubule-targeting agents can be divided into two groups: microtubule-stabilizing, and microtubule-destabilizing agents. The former bind to the tubulin polymer and stabilize microtubules, while the latter bind to the tubulin dimers and destabilize microtubules. Alteration of tubulin-microtubule equilibrium determines the disruption of the mitotic spindle, halting the cell cycle at the metaphase-anaphase transition and, eventually, resulting in cell death. Clinical application of earlier microtubule inhibitors, however, unfortunately showed several limits, such as neurological and bone marrow toxicity and the emergence of drug-resistant tumor cells. Here we review several natural and synthetic microtubule-targeting agents, which showed antitumor activity and increased efficacy in comparison to traditional drugs in various preclinical and clinical studies. Cryptophycins, combretastatins, ombrabulin, soblidotin, D-24851, epothilones and discodermolide were used in clinical trials. Some of them showed antiangiogenic and antivascular activity and others showed the ability to overcome multidrug resistance, supporting their possible use in chemotherapy.

Fanale, D., Bronte, G., Passiglia, F., Calò, V., Castiglia, M., Di Piazza, F., et al. (2015). Stabilizing versus destabilizing the microtubules: A double-edge sword for an effective cancer treatment option?. ANALYTICAL CELLULAR PATHOLOGY, 2015 [10.1155/2015/690916].

Stabilizing versus destabilizing the microtubules: A double-edge sword for an effective cancer treatment option?

FANALE, Daniele
;
BRONTE, Giuseppe;PASSIGLIA, Francesco;CALO', Valentina;CASTIGLIA, Marta;DI PIAZZA, Florinda;Barraco, Nadia;Cangemi, Antonina;CATARELLA, Maria Teresa;INSALACO, Lavinia;LISTI', Angela;Massihnia, Daniela;Perez, Alessandro;TOIA, Francesca;CICERO, Giuseppe;BAZAN, Viviana
2015

Abstract

Microtubules are dynamic and structural cellular components involved in several cell functions, including cell shape, motility, and intracellular trafficking. In proliferating cells, they are essential components in the division process through the formation of the mitotic spindle. As a result of these functions, tubulin and microtubules are targets for anticancer agents. Microtubule-targeting agents can be divided into two groups: microtubule-stabilizing, and microtubule-destabilizing agents. The former bind to the tubulin polymer and stabilize microtubules, while the latter bind to the tubulin dimers and destabilize microtubules. Alteration of tubulin-microtubule equilibrium determines the disruption of the mitotic spindle, halting the cell cycle at the metaphase-anaphase transition and, eventually, resulting in cell death. Clinical application of earlier microtubule inhibitors, however, unfortunately showed several limits, such as neurological and bone marrow toxicity and the emergence of drug-resistant tumor cells. Here we review several natural and synthetic microtubule-targeting agents, which showed antitumor activity and increased efficacy in comparison to traditional drugs in various preclinical and clinical studies. Cryptophycins, combretastatins, ombrabulin, soblidotin, D-24851, epothilones and discodermolide were used in clinical trials. Some of them showed antiangiogenic and antivascular activity and others showed the ability to overcome multidrug resistance, supporting their possible use in chemotherapy.
Settore MED/06 - Oncologia Medica
Fanale, D., Bronte, G., Passiglia, F., Calò, V., Castiglia, M., Di Piazza, F., et al. (2015). Stabilizing versus destabilizing the microtubules: A double-edge sword for an effective cancer treatment option?. ANALYTICAL CELLULAR PATHOLOGY, 2015 [10.1155/2015/690916].
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10447/152042
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