Evidence map›Paper›PMID 30264192›Full record

ArticleMolecular genetics and genomics : MGG2019

Proliferation of aneuploid cells induced by CENP-E depletion is counteracted by the p14

Lorena Veneziano, Viviana Barra, Danilo Cilluffo, Aldo Di Leonardo

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular genetics and genomics : MGG, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. P14Genes · 2020
    Article
  7. Investigating REPAIRv2 as a Tool to EditInternational journal of molecular sciences · 2020
    Article
  8. 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 at 3 institutions in 2 countries.

Lorena VenezianoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy.
Viviana BarraDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy.
Danilo CilluffoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy.
Aldo Di LeonardoDepartment of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Palermo, Italy. aldo.dileonardo@unipa.it.ORCID http://orcid.org/0000-0003-4760-7179
University of Palermo · ITCentre National de la Recherche Scientifique · FRIstituto Sperimentale per la Frutticoltura · IT

Funding

University of Palermo ATE-0255
6 · The paper itself

Abstract

The spindle assembly checkpoint (SAC) is a cellular surveillance mechanism that ensures the fidelity of chromosomes segregation. Reduced expression of some of its components weakens the SAC and induces chromosome instability and aneuploidy, which are both well-known hallmarks of cancer cells. Centromere protein-E (CENP-E) is a crucial component of the SAC and its function is to facilitate kinetochore microtubule attachment required to achieve and maintain chromosome alignment. The present study investigates the possible role of p14

Indexed as

AneuploidyCell LineCell ProliferationCell SurvivalChromosomal Proteins, Non-HistoneFibroblastsGenes, Tumor SuppressorHCT116 CellsHumansM Phase Cell Cycle CheckpointsOncogene ProteinsRNA, Small InterferingCDK2AP2 protein, humancentromere protein EChromosomal Proteins, Non-HistoneOncogene ProteinsRNA, Small InterferingAneuploidyCENP-EHCT116 cellsP14ARFRNAi

Identifiers

PMID30264192
OpenAlexW2893453799

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.