Evidence map›Paper›PMID 30872646›Full record

ArticleScientific reports2019

Primary neurons can enter M-phase.

Chaska C Walton, Wei Zhang, Iris Patiño-Parrado, Estíbaliz Barrio-Alonso, Juan-José Garrido, José M Frade

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.8field-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

21 citing papers in PubMed, 35 citations in OpenAlex.

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  19. Cell Cycle Proteins as Key Regulators of Postmitotic Cell Death.The Yale journal of biology and medicine · 2019
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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

6 authors at 1 institution in 1 country.

Chaska C WaltonDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain.ORCID 0000-0001-8513-0207
Wei ZhangDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain.
Iris Patiño-ParradoDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain.
Estíbaliz Barrio-AlonsoDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain.
Juan-José GarridoDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain.
José M FradeDepartment of Molecular, Cellular and Developmental Neurobiology, Cajal Institute (CSIC), Madrid, 28002, Spain. frade@cajal.csic.es.
Instituto Cajal · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Differentiated neurons can undergo cell cycle re-entry during pathological conditions, but it remains largely accepted that M-phase is prohibited in these cells. Here we show that primary neurons at post-synaptogenesis stages of development can enter M-phase. We induced cell cycle re-entry by overexpressing a truncated Cyclin E isoform fused to Cdk2. Cyclin E/Cdk2 expression elicits canonical cell cycle checkpoints, which arrest cell cycle progression and trigger apoptosis. As in mitotic cells, checkpoint abrogation enables cell cycle progression through S and G2-phases into M-phase. Although most neurons enter M-phase, only a small subset undergo cell division. Alternatively, neurons can exit M-phase without cell division and recover the axon initial segment, a structural determinant of neuronal viability. We conclude that neurons and mitotic cells share S, G2 and M-phase regulation.

Indexed as

Cell DivisionApoptosisCell Cycle ProteinsCell DifferentiationCyclin-Dependent Kinase 2Cyclin ECytokinesisG2 PhaseHumansNeuronsOncogene ProteinsProtein-Tyrosine KinasesTumor Suppressor Protein p53CCNE1 protein, humanCDK2 protein, humanCell Cycle ProteinsCyclin-Dependent Kinase 2Cyclin EOncogene ProteinsProtein-Tyrosine KinasesTP53 protein, humanTumor Suppressor Protein p53WEE1 protein, human

Identifiers

PMID30872646
PMCPMC6418114
OpenAlexW2920993016

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.