Literature DB >> 22352901

A cell-based assay for screening spindle checkpoint inhibitors.

Zhen Hua Wu1, Long Yu Hu, Da Qian Xu, Xiaotong Li.   

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.

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Year:  2012        PMID: 22352901      PMCID: PMC3421965          DOI: 10.1089/adt.2011.416

Source DB:  PubMed          Journal:  Assay Drug Dev Technol        ISSN: 1540-658X            Impact factor:   1.738


  25 in total

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3.  Pharmacologic abrogation of the mitotic spindle checkpoint by an indolocarbazole discovered by cellular screening efficiently kills cancer cells.

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6.  Complete loss of the tumor suppressor MAD2 causes premature cyclin B degradation and mitotic failure in human somatic cells.

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Review 8.  The spindle checkpoint, aneuploidy, and cancer.

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Journal:  Oncogene       Date:  2004-03-15       Impact factor: 9.867

Review 9.  The spindle-assembly checkpoint in space and time.

Authors:  Andrea Musacchio; Edward D Salmon
Journal:  Nat Rev Mol Cell Biol       Date:  2007-04-11       Impact factor: 94.444

10.  Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores.

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Journal:  J Cell Biol       Date:  2003-04-28       Impact factor: 10.539

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Review 2.  Evolving Therapeutic Strategies to Exploit Chromosome Instability in Cancer.

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