Microtubule stabilizing agents: their molecular signaling consequences and the potential for enhancement by drug combination
Abstract
Microtubule stabilization by chemotherapy is a powerful weapon in the war against cancer. Disruption of the mitotic spindle activates a number of signaling pathways, with consequences that may protect the cell or lead to its death via apoptosis. Taxol, the first microtubule stabilizing drug to be identified, has been utilized successfully in the treatment of solid tumors for two decades. Several features, however, make this drug less than ideal, and the search for next generation stabilizing drugs with increased efficacy has been intense and fruitful. Microtubule stabilizing agents (MSAs), including the taxanes, the epothilones, discodermolide, laulimalide, and eleutherobin, form an important and expanding family of chemotherapeutic agents. A strong understanding of their molecular signaling consequences is essential to their value, particularly in regard to their potential for combinatorial chemotherapy - the use of multiple agents to enhance the efficacy of cancer treatment. Here we present a critical review of research on the signaling mechanisms induced by MSAs, their relevance to apoptosis, and their potential for exploitation by combinatorial therapy.
References
Citations
Concentration-dependent differential effects of an epothilone analog on cell cycle and p53 signaling
Targeting prostate cancer with HTI-286, a synthetic analog of the marine sponge product hemiasterlin
Exploiting the cytoskeletal filaments of neoplastic cells to potentiate a novel therapeutic approach
Autotaxin protects MCF-7 breast cancer and MDA-MB-435 melanoma cells against Taxol-induced apoptosis
Nordihydroguaiaretic acid affects multiple dynein-dynactin functions in interphase and mitotic cells
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