Evidence map›Paper›PMID 20195506›Full record

ArticlePLoS genetics2010

Cdk2 is required for p53-independent G2/M checkpoint control.

Jon H Chung, Fred Bunz

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 101 citations in OpenAlex.

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  8. iScience · 2023
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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 1 country.

Jon H ChungDepartment of Radiation Oncology and Molecular Radiation Sciences and The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Fred Bunz
Johns Hopkins University · USSidney Kimmel Comprehensive Cancer Center · US

Funding

DNA Damaging Signaling in Human Cancer CellsR01CA104253 · NCI · JOHNS HOPKINS UNIVERSITY · PI BUNZ, FRED · 2004 to 2007
$1.1M
NCI NIH HHS CA104253NCI NIH HHS R01 CA104253
6 · The paper itself

Abstract

The activation of phase-specific cyclin-dependent kinases (Cdks) is associated with ordered cell cycle transitions. Among the mammalian Cdks, only Cdk1 is essential for somatic cell proliferation. Cdk1 can apparently substitute for Cdk2, Cdk4, and Cdk6, which are individually dispensable in mice. It is unclear if all functions of non-essential Cdks are fully redundant with Cdk1. Using a genetic approach, we show that Cdk2, the S-phase Cdk, uniquely controls the G(2)/M checkpoint that prevents cells with damaged DNA from initiating mitosis. CDK2-nullizygous human cells exposed to ionizing radiation failed to exclude Cdk1 from the nucleus and exhibited a marked defect in G(2)/M arrest that was unmasked by the disruption of P53. The DNA replication licensing protein Cdc6, which is normally stabilized by Cdk2, was physically associated with the checkpoint regulator ATR and was required for efficient ATR-Chk1-Cdc25A signaling. These findings demonstrate that Cdk2 maintains a balance of S-phase regulatory proteins and thereby coordinates subsequent p53-independent G(2)/M checkpoint activation.

Indexed as

G2 PhaseMitosisAnimalsAtaxia Telangiectasia Mutated Proteinscdc25 PhosphatasesCell Cycle ProteinsCheckpoint Kinase 1Cyclin-Dependent Kinase 2CytoplasmEnzyme ActivationEnzyme StabilityHCT116 CellsHumansMiceModels, BiologicalNuclear ProteinsAtaxia Telangiectasia Mutated ProteinsATR protein, humancdc25 PhosphatasesCDC6 protein, humanCDK2 protein, humanCell Cycle ProteinsCheckpoint Kinase 1CHEK1 protein, humanChek1 protein, mouseCyclin-Dependent Kinase 2Nuclear ProteinsProtein KinasesProtein Serine-Threonine KinasesTumor Suppressor Protein p53

Identifiers

PMID20195506
PMCPMC2829054
OpenAlexW2093147524

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.