Kolesnick Richard, Altieri Dario, Fuks Zvi
Program of Molecular Pharmacology and Chemistry, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Cancer Cell. 2007 Jun;11(6):473-5. doi: 10.1016/j.ccr.2007.05.003.
An unexpected benefit of functional genomic screens is that at times they answer questions that they were not designed to ask. A siRNA screen reported by Swanton et al. in this issue of Cancer Cell reveals that silencing of spindle assembly checkpoint genes facilitates mitotic slippage, resulting in escape from taxane-induced cell death, aneuploidy, and chromosomal instability, hallmarks of taxane resistance. Unexpectedly, the screen disclosed that the sphingolipid ceramide is a key regulator of the taxane-mediated spindle assembly checkpoint and taxane-induced cell death. Ceramide metabolism thus serves as a legitimate target for modulation of taxane effect on tumors.
功能基因组筛选的一个意外好处是,有时它们能回答一些并非其设计初衷的问题。斯旺顿等人在本期《癌细胞》杂志上报道的一项小干扰RNA筛选显示,纺锤体组装检查点基因的沉默会促进有丝分裂期滑脱,导致细胞逃脱紫杉烷诱导的细胞死亡、非整倍体和染色体不稳定,这些都是紫杉烷耐药的标志。出乎意料的是,该筛选还揭示,鞘脂神经酰胺是紫杉烷介导的纺锤体组装检查点和紫杉烷诱导的细胞死亡的关键调节因子。因此,神经酰胺代谢可作为调节紫杉烷对肿瘤作用的合理靶点。