Evidence map›Paper›PMID 27398835›Full record

ArticleCell cycle (Georgetown, Tex.)2016

PTEN regulates PLK1 and controls chromosomal stability during cell division.

Zhong Zhang, Sheng-Qi Hou, Jinxue He, Tingting Gu, Yuxin Yin, Wen H Shen

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  8. Review
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  13. Article
  14. PTEN as a Guardian of the Genome: Pathways and Targets.Cold Spring Harbor perspectives in medicine · 2020
    Review
  15. Posttranslational Regulation and Conformational Plasticity of PTEN.Cold Spring Harbor perspectives in medicine · 2020
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 2 countries.

Zhong Zhanga Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Sheng-Qi Houa Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Jinxue Hea Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Tingting Gua Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Yuxin Yina Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Wen H Shena Department of Radiation Oncology , Weill Medical Medicine, Cornell University , New York , NY , USA.
Cornell University · US

Funding

Role of PTEN in Mitosis and Chromosome StabilityR01GM100478 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI SHEN, WEN H. · 2012 to 2020
$2.9M
6 · The paper itself

Abstract

PTEN functions as a guardian of the genome through multiple mechanisms. We have previously established that PTEN maintains the structural integrity of chromosomes. In this report, we demonstrate a fundamental role of PTEN in controlling chromosome inheritance to prevent gross genomic alterations. Disruption of PTEN or depletion of PTEN protein phosphatase activity causes abnormal chromosome content, manifested by enlarged or polyploid nuclei. We further identify polo-like kinase 1 (PLK1) as a substrate of PTEN phosphatase. PTEN can physically associate with PLK1 and reduce PLK1 phosphorylation in a phosphatase-dependent manner. We show that PTEN deficiency leads to PLK1 phosphorylation and that a phospho-mimicking PLK1 mutant causes polyploidy, imitating functional deficiency of PTEN phosphatase. Inhibition of PLK1 activity or overexpression of a non-phosphorylatable PLK1 mutant reduces the polyploid cell population. These data reveal a new mechanism by which PTEN controls genomic stability during cell division.

Indexed as

Cell DivisionChromosomal InstabilityAnimalsCell Cycle ProteinsEnzyme ActivationEnzyme StabilityHeLa CellsHumansKaryotypingMiceMitosisNocodazolePhosphorylationPolo-Like Kinase 1PolyploidyProtein Serine-Threonine KinasesCell Cycle ProteinsNocodazolePolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsPTEN PhosphohydrolasePTEN protein, humanPten protein, mousechromosome stabilityMitosisphosphorylationpolyploidyPTEN; polo-like kinase 1

Identifiers

PMID27398835
PMCPMC5026806
OpenAlexW2474488847

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.