Evidence map›Paper›PMID 32347795›Full record

ArticleeLife2020

Asymmetric clustering of centrosomes defines the early evolution of tetraploid cells.

Nicolaas C Baudoin, Joshua M Nicholson, Kimberly Soto, Olga Martin, Jing Chen, Daniela Cimini

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Oxidative stress and serum deprivation influence the evolution of newly formed tetraploid cells during tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  9. Whole-genome doubling in tissues and tumors.Trends in genetics : TIG · 2023
    Review
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  13. Whole-Genome Doubling as a source of cancer: how, when, where, and why?Frontiers in cell and developmental biology · 2023
    Review
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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 2 countries.

Nicolaas C BaudoinDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.ORCID 0000-0003-3316-5293
Joshua M NicholsonDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.
Kimberly SotoDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.
Olga MartinDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.
Jing ChenDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.ORCID 0000-0001-6321-0505
Daniela CiminiDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, United States.ORCID 0000-0002-4082-4894
Institute of Cancer Research · GB

Funding

Fralin Life Sciences Institute Discretionary fundsICTAS Center for Engineered Health Seed fundingNational Science Foundation MCB-1517506Virginia Tech BIOTRANS IGEPVirginia Tech College of Science Dean's Discovery FundVirginia Tech Fralin Life Sciences Institute Discretionary fundsVirginia Tech ICTAS Center for Engineered Health Seed fundingVirginia Tech College of Science Dean's Discovery FundVirginia Tech Graduate School BIOTRANS IGEP
6 · The paper itself

Abstract

Tetraploidy has long been of interest to both cell and cancer biologists, partly because of its documented role in tumorigenesis. A common model proposes that the extra centrosomes that are typically acquired during tetraploidization are responsible for driving tumorigenesis. However, tetraploid cells evolved in culture have been shown to lack extra centrosomes. This observation raises questions about how tetraploid cells evolve and more specifically about the mechanisms(s) underlying centrosome loss. Here, using a combination of fixed cell analysis, live cell imaging, and mathematical modeling, we show that populations of newly formed tetraploid cells rapidly evolve in vitro to retain a near-tetraploid chromosome number while losing the extra centrosomes gained at the time of tetraploidization. This appears to happen through a process of natural selection in which tetraploid cells that inherit a single centrosome during a bipolar division with asymmetric centrosome clustering are favored for long-term survival.

Indexed as

TetraploidyAneuploidyCarcinogenesisCells, CulturedCentrosomeEvolution, MolecularHumansMitosisModels, TheoreticalSelection, Geneticcell biologycell divisioncentrosomesnonetetraploidy

Identifiers

PMID32347795
PMCPMC7250578
OpenAlexW3019629603

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.