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Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/4756

Title: Bcl-2 inhibitors: small molecules with a big impact on cancer therapy
Authors: Vogler, Meike
Dinsdale, David
Dyer, Martin J.S.
Cohen, Gerald M.
Issue Date: Mar-2009
Publisher: Nature Publishing Group
Citation: Cell Death and Differentiation, 2009, 16 (3), pp. 360-367.
Abstract: Despite tremendous advances over the last 15 years in understanding fundamental mechanisms of apoptosis, this has failed to translate into improved cancer therapy for patients. However, there may now be light at the end of this long tunnel. Antiapoptotic Bcl-2 family members may be divided into two subclasses, one comprising Bcl-2, Bcl-XL and Bcl-w and the other Mcl-1 and Bcl2A1. Neutralization of both subclasses is required for apoptosis induction. Solution of the structure of antiapoptotic Bcl-2 family proteins has led to the design of novel small molecule inhibitors. Although many such molecules have been synthesized, rigorous verification of their specificity has often been lacking. Further studies have revealed that many putative Bcl-2 inhibitors are not specific and have other cellular targets, resulting in non-mechanism based toxicity. Two notable exceptions are ABT-737 and a related orally active derivative, ABT-263, which bind with high affinity to Bcl-2, Bcl-XL and Bcl-w and may prove to be useful tools for mechanistic studies. ABT-263 is in early clinical trials in lymphoid malignancies, small-cell lung cancer and chronic lymphocytic leukemia, and some patients have shown promising results. In in vitro studies, primary cells from patients with various B-cell malignancies are exquisitely sensitive to ABT-737, exhibiting novel morphological features of apoptosis including marked outer mitochondrial membrane rupture.
ISSN: 1350-9047
Links: http://dx.doi.org/10.1038/cdd.2008.137
http://hdl.handle.net/2381/4756
Type: Article
Description: This is the author's final draft of the paper published as Cell Death and Differentiation, 2009, 16 (3), pp. 360-367. The final version is available from http://www.nature.com/cdd/journal/v16/n3/abs/cdd2008137a.html. Doi: 10.1038/cdd.2008.137
Appears in Collections:Published Articles, MRC Toxicology Unit

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