McConkey David J
Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Cancer Cell. 2008 Jul 8;14(1):1-2. doi: 10.1016/j.ccr.2008.06.011.
In this issue of Cancer Cell, Nickeleit et al. (2008) identify a new proteasome inhibitor, argyrin A, and show that it induces apoptosis and inhibits angiogenesis via p27-dependent mechanisms. Their observations challenge current thinking about how this class of promising cancer therapies works and why they selectively kill cancer cells.
在本期《癌细胞》杂志中,尼克莱特等人(2008年)鉴定出一种新的蛋白酶体抑制剂——银霉素A,并表明它通过依赖p27的机制诱导细胞凋亡并抑制血管生成。他们的观察结果挑战了目前关于这类有前景的癌症治疗方法如何起作用以及为何它们能选择性杀死癌细胞的观点。