Evidence map›Paper›PMID 22352901›Full record

ArticleAssay and drug development technologies2012

A cell-based assay for screening spindle checkpoint inhibitors.

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

Abstract read
In one paragraph

Article in Assay and drug development technologies, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Zhen Hua WuSchool of Life Sciences, Xiamen University, Xiamen, Fujian, P.R. China.
Long Yu Hu
Da Qian Xu
Xiaotong Li

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Antineoplastic AgentsAurora KinasesBlotting, WesternCell CycleCell Cycle CheckpointsCell LineColoring AgentsDose-Response Relationship, DrugDrug Evaluation, PreclinicalDrug Screening Assays, AntitumorEnzyme InhibitorsFluorescent Antibody TechniqueHeLa CellsHigh-Throughput Screening AssaysHumansMitotic IndexAntineoplastic AgentsAurora KinasesColoring AgentsEnzyme InhibitorsNocodazoleProtein Serine-Threonine KinasesPurinesRoscovitineTetrazolium SaltsThiazolesthiazolyl blue

Identifiers

PMID22352901
PMCPMC3421965

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.