Evidence map›Paper›PMID 25789599›Full record

ReviewCell cycle (Georgetown, Tex.)2015

A role of WT1 in cell division and genomic stability.

Jayasha Shandilya, Stefan G E Roberts

Open access · bronzeAbstract readReview
In one paragraph

Review in Cell cycle (Georgetown, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  8. Review
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  14. Article
  15. Prognostic Impact of WT-1 Gene Expression in Egyptian Children with Acute Lymphoblastic Leukemia.Mediterranean journal of hematology and infectious diseases · 2016
    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

2 authors at 2 institutions in 2 countries.

Jayasha Shandilyaa Department of Biological Sciences ; University at Buffalo ; Buffalo , NY USA.
Stefan G E Roberts
At Bristol · GBUniversity at Buffalo, State University of New York · US

Funding

Functional analysis of the WT1-BASP1 transcriptional repressor complexR01GM098609 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MEDLER, KATHRYN, ROBERTS, STEFAN · 2012 to 2015
$1.2M
NIGMS NIH HHS R01 GM098609
6 · The paper itself

Abstract

Wilms' tumor-1 protein (WT1) is a transcription factor that can either activate or repress genes to regulate cell growth, apoptosis and differentiation. WT1 can act as either a tumor suppressor or an oncogene. The cellular functions of WT1 are predominantly regulated by its various interacting partners. Recently we have found that WT1 can regulate the fidelity of chromosome segregation through its interaction with the spindle assembly checkpoint protein, Mitotic arrest deficient-2 (MAD2). WT1 delays anaphase entry by inhibiting the ubiquitination activity of the Anaphase promoting complex/cyclosome (APC/C). Our findings have revealed an important role of WT1 in the regulation of mitotic checkpoint and genomic stability.

Indexed as

Cell Cycle CheckpointsGenomic InstabilityAnaphase-Promoting Complex-CyclosomeAnimalsCell Cycle ProteinsChromosome SegregationHumansMad2 ProteinsMitosisSignal TransductionTumor Suppressor Protein p53WT1 ProteinsAnaphase-Promoting Complex-CyclosomeCell Cycle ProteinsMAD2L1 protein, humanMad2 ProteinsTP53 protein, humanTumor Suppressor Protein p53WT1 ProteinscheckpointMad2mitosisWT1

Identifiers

PMID25789599
PMCPMC4614692
OpenAlexW1541989388

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.