| Literature DB >> 27348355 |
María-Jesús Pérez-Pérez1, Eva-María Priego1, Oskía Bueno1, Maria Solange Martins2, María-Dolores Canela1, Sandra Liekens2.
Abstract
The unique characteristics of the tumor vasculature offer the possibility to selectively target tumor growth and vascularization using tubulin-destabilizing agents. Evidence accumulated with combretastatin A-4 (CA-4) and its prodrug CA-4P support the therapeutic value of compounds sharing this mechanism of action. However, the chemical instability and poor solubility of CA-4 demand alternative compounds that are able to surmount these limitations. This Perspective illustrates the different classes of compounds that behave similar to CA-4, analyzes their binding mode to αβ-tubulin according to recently available structural complexes, and includes described approaches to improve their delivery. In addition, dissecting the mechanism of action of CA-4 and analogues allows a closer insight into the advantages and drawbacks associated with these tubulin-destabilizing agents that behave as vascular disrupting agents (VDAs).Entities:
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Year: 2016 PMID: 27348355 DOI: 10.1021/acs.jmedchem.6b00463
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446