TY - JOUR
T1 - Exploring the Mechanisms of Action of the Novel Microtubule Inhibitor Vinflunine
AU - Jordan, Mary Ann
AU - Horwitz, Susan Band
AU - Lobert, Sharon
AU - Correia, John J.
PY - 2008/6/1
Y1 - 2008/6/1
N2 - Microtubules have been identified as a suitable target for anticancer therapy, primarily based on their biological importance in coordinating chromosomal segregation at mitosis. Two main classes of microtubule-targeted agents, the taxanes and vinca alkaloids, suppress the dynamic behavior of spindle microtubules, inducing mitotic arrest and subsequent apoptotic cell death. Clinical activity of taxanes and first-generation vinca alkaloids in the treatment of solid tumors and hematologic malignancies, respectively, has prompted further research for novel analogs with improved clinical efficacy and safety. Such efforts have led to the development of vinflunine, a bifluorinated vinca alkaloid endowed with unique antitumor properties. Highlighted in this review are the key features of vinflunine that lead to effective suppression of microtubule dynamics and induction of cell death in cancer cells.
AB - Microtubules have been identified as a suitable target for anticancer therapy, primarily based on their biological importance in coordinating chromosomal segregation at mitosis. Two main classes of microtubule-targeted agents, the taxanes and vinca alkaloids, suppress the dynamic behavior of spindle microtubules, inducing mitotic arrest and subsequent apoptotic cell death. Clinical activity of taxanes and first-generation vinca alkaloids in the treatment of solid tumors and hematologic malignancies, respectively, has prompted further research for novel analogs with improved clinical efficacy and safety. Such efforts have led to the development of vinflunine, a bifluorinated vinca alkaloid endowed with unique antitumor properties. Highlighted in this review are the key features of vinflunine that lead to effective suppression of microtubule dynamics and induction of cell death in cancer cells.
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U2 - 10.1053/j.seminoncol.2008.01.009
DO - 10.1053/j.seminoncol.2008.01.009
M3 - Article
C2 - 18538179
AN - SCOPUS:44449128533
SN - 0093-7754
VL - 35
SP - S6-S12
JO - Seminars in Oncology
JF - Seminars in Oncology
IS - SUPPL 3
ER -