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STX140 and STX641 cause apoptosis via the intrinsic mitochondrial pathway and down-regulate survivin and XIAP expression in ovarian and prostate cancer cells.

Authors :
Foster PA
Ho YT
Newman SP
Leese MP
Potter BV
Reed MJ
Purohit A
Source :
Anticancer research [Anticancer Res] 2009 Oct; Vol. 29 (10), pp. 3751-7.
Publication Year :
2009

Abstract

Many anticancer drugs target microtubules and induce apoptosis. However, improved microtubule-targeting drugs, such as STX140 and STX641, are being developed. These compounds induce cell cycle arrest and apoptosis in a variety of tumour cells. The mechanisms that induce apoptosis and the key mediators involved are elucidated in this study. Results demonstrate that STX140 and STX641 depolarise mitochondrial bioenergetics and activate caspase 3/7 in A2780, LNCaP and MCF-7 cancer cells. Furthermore, both compounds cause a significant reduction in the expression of survivin and XIAP. This work details the temporal organisation of apoptosis induced by two microtubule disruptors and highlights the role that the down-regulation of survivin and XIAP may play in this process.

Details

Language :
English
ISSN :
1791-7530
Volume :
29
Issue :
10
Database :
MEDLINE
Journal :
Anticancer research
Publication Type :
Academic Journal
Accession number :
19846905