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一种用于筛选纺锤体检查点抑制剂的基于细胞的检测方法。

A cell-based assay for screening spindle checkpoint inhibitors.

作者信息

Wu Zhen Hua, Hu Long Yu, Xu Da Qian, Li Xiaotong

机构信息

School of Life Sciences, Xiamen University, Xiamen, Fujian, P.R. China.

出版信息

Assay Drug Dev Technol. 2012 Aug;10(4):344-52. doi: 10.1089/adt.2011.416. Epub 2012 Feb 21.

DOI:10.1089/adt.2011.416
PMID:22352901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3421965/
Abstract

In eukaryotes, the spindle checkpoint acts as a surveillance mechanism that ensures faithful chromosome segregation. The spindle checkpoint prevents premature separation of sister chromatids and the onset of anaphase until every chromosome is properly attached to the mitotic spindle. Tumorigenesis might result from generation of aneuploidy by dysfunction of the spindle checkpoint. Differences of the checkpoint system in normal cells versus tumor cells might provide a new opportunity in cancer drug development; therefore, efforts to identify the spindle checkpoint inhibitors have been fostered. Based on spindle checkpoint inhibitors being able to induce cells to exit mitotic arrest caused by microtubule drug treatment, we developed a cell-based assay to screen compounds that were potential spindle checkpoint inhibitors. This assay was validated with a known spindle checkpoint inhibitor and was easy to adapt to a large-scale screening. It also had the advantages of being high in sensitivity and low in cost.

摘要

在真核生物中,纺锤体检查点作为一种监测机制,确保染色体准确分离。纺锤体检查点可防止姐妹染色单体过早分离以及后期的开始,直到每条染色体都正确地附着在有丝分裂纺锤体上。肿瘤发生可能是由于纺锤体检查点功能障碍导致非整倍体的产生。正常细胞与肿瘤细胞中检查点系统的差异可能为癌症药物开发提供新的机会;因此,人们一直在努力寻找纺锤体检查点抑制剂。基于纺锤体检查点抑制剂能够诱导细胞退出由微管药物处理引起的有丝分裂停滞,我们开发了一种基于细胞的检测方法来筛选潜在的纺锤体检查点抑制剂化合物。该检测方法已用一种已知的纺锤体检查点抑制剂进行了验证,并且易于适应大规模筛选。它还具有灵敏度高和成本低的优点。

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本文引用的文献

1
Pharmacologic abrogation of the mitotic spindle checkpoint by an indolocarbazole discovered by cellular screening efficiently kills cancer cells.通过细胞筛选发现的一种吲哚咔唑对有丝分裂纺锤体检查点进行药理学消除,可有效杀死癌细胞。
Cancer Res. 2009 May 1;69(9):3874-83. doi: 10.1158/0008-5472.CAN-08-3597. Epub 2009 Apr 14.
2
A high throughput, whole cell screen for small molecule inhibitors of the mitotic spindle checkpoint identifies OM137, a novel Aurora kinase inhibitor.一项针对有丝分裂纺锤体检查点小分子抑制剂的高通量全细胞筛选鉴定出了一种新型极光激酶抑制剂OM137。
Cancer Res. 2009 Feb 15;69(4):1509-16. doi: 10.1158/0008-5472.CAN-08-3133. Epub 2009 Feb 3.
3
Structure-based drug design of novel Aurora kinase A inhibitors: structural basis for potency and specificity.新型极光激酶A抑制剂的基于结构的药物设计:效力和特异性的结构基础
J Med Chem. 2009 Feb 26;52(4):1050-62. doi: 10.1021/jm801270e.
4
Aurora kinases as targets for cancer therapy.极光激酶作为癌症治疗的靶点。
Cancer Treat Rev. 2008 Apr;34(2):175-82. doi: 10.1016/j.ctrv.2007.09.005. Epub 2007 Nov 19.
5
The spindle-assembly checkpoint in space and time.时空维度下的纺锤体组装检查点
Nat Rev Mol Cell Biol. 2007 May;8(5):379-93. doi: 10.1038/nrm2163. Epub 2007 Apr 11.
6
A census of mitotic cancer genes: new insights into tumor cell biology and cancer therapy.有丝分裂癌症基因普查:对肿瘤细胞生物学和癌症治疗的新见解。
Carcinogenesis. 2007 May;28(5):899-912. doi: 10.1093/carcin/bgm019. Epub 2007 Jan 27.
7
Roles of Aurora kinases in mitosis and tumorigenesis.极光激酶在有丝分裂和肿瘤发生中的作用。
Mol Cancer Res. 2007 Jan;5(1):1-10. doi: 10.1158/1541-7786.MCR-06-0208.
8
The anaphase promoting complex/cyclosome: a machine designed to destroy.后期促进复合物/细胞周期体:一台旨在破坏的机器。
Nat Rev Mol Cell Biol. 2006 Sep;7(9):644-56. doi: 10.1038/nrm1988. Epub 2006 Aug 9.
9
Lethality to human cancer cells through massive chromosome loss by inhibition of the mitotic checkpoint.通过抑制有丝分裂检查点导致大规模染色体丢失从而对人类癌细胞产生致死性。
Proc Natl Acad Sci U S A. 2004 Jun 8;101(23):8699-704. doi: 10.1073/pnas.0401142101. Epub 2004 May 24.
10
Complete loss of the tumor suppressor MAD2 causes premature cyclin B degradation and mitotic failure in human somatic cells.肿瘤抑制因子MAD2的完全缺失会导致人类体细胞中细胞周期蛋白B过早降解和有丝分裂失败。
Proc Natl Acad Sci U S A. 2004 Mar 30;101(13):4459-64. doi: 10.1073/pnas.0306069101. Epub 2004 Mar 15.