Table 1.
Microtubule Inhibitors | Binding Domains | Cancer Treatments | Mode of Action | References |
---|---|---|---|---|
Paclitaxel (nab-paclitaxel) | Taxane-binding | Breast, ovarian, prostate, lung | Anti-microtubule depolymerization leading to mitotic arrest | [12,20] |
Docetaxel | Taxane-binding | Breast, non-small cell lung, androgen-independent metastatic prostate cancer | Anti-microtubule depolymerization, and attenuation of bcl-2 and bcl-xL gene expression | [21,22] |
Colchicine * | Colchicine-binding | Hepatocellular & prostate cancers | Anti-microtubule polymerization. Cell cycle arrest in metaphase | [19,23,24,25] |
Vinblastine | Vinca-binding | Testicular, Hodgkins and non-Hodgkins lymphoma, breast, & germ cell cancers. | Induces wedge at tubulin interface causing tubulin self-association into spiral aggregates. Anti-microtubule polymerization, & cell cycle arrest in metaphase. | [17,26] |
* Colchicine is often administered for the treatment of gout as it was FDA approved for this condition in 2009. While colchicine has not yet been approved for cancer treatment, it was shown to decrease cancer incidence in male gout patients [25].