Sturgeon Christopher M, Craig Kyle, Brown Colleen, Rundle Natalie T, Andersen Raymond J, Roberge Michel
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3.
Planta Med. 2005 Oct;71(10):938-43. doi: 10.1055/s-2005-873109.
A phenotypic cell-based assay for inhibitors of the G (2) DNA damage checkpoint was used to screen plant extracts from the US National Cancer Institute Natural Products Repository. It revealed activity in a methanol extract from the common ragweed Ambrosia artemisiifolia. Assay-guided fractionation led to the identification of the sesquiterpene lactones psilostachyins A and C as novel checkpoint inhibitors. Elimination of their alpha,beta-unsaturated carbonyl group caused a loss of activity, suggesting that the compounds can bind covalently to target proteins through Michael addition. Psilostachyins A and C also blocked cells in mitosis and caused the formation of aberrant microtubule spindles. However, the compounds did not interfere with microtubule polymerization in vitro. The related sesquiterpene lactones psilostachyin B, paulitin and isopaulitin were also isolated from the same extract but showed no checkpoint inhibition. The identification of the target(s) of psilostachyins A and C may provide further insight into the signalling pathways involved in cell cycle arrest and mitotic progression.
采用基于细胞表型的检测方法筛选G(2)期DNA损伤检查点抑制剂,以检测美国国立癌症研究所天然产物库中的植物提取物。结果显示,来自豚草的甲醇提取物具有活性。通过检测指导的分级分离,鉴定出倍半萜内酯psilostachyins A和C为新型检查点抑制剂。消除其α,β-不饱和羰基会导致活性丧失,这表明这些化合物可通过迈克尔加成与靶蛋白共价结合。Psilostachyins A和C还能使细胞阻滞在有丝分裂期,并导致异常微管纺锤体的形成。然而,这些化合物在体外并不干扰微管聚合。还从同一提取物中分离出了相关的倍半萜内酯psilostachyin B、paulitin和异paulitin,但它们没有显示出检查点抑制作用。鉴定psilostachyins A和C的靶标可能会为深入了解细胞周期停滞和有丝分裂进程中涉及的信号通路提供更多线索。