Evidence map›Paper›PMID 41570321›Full record

ArticleCancer research2026

Cell and Nuclear Size Is Associated with Chromosomal Instability and Tumorigenicity in Cancer Cells That Undergo Whole Genome Doubling.

Mathew Bloomfield, Sydney M Huth, Daniella S McCausland, Ron Saad, Nazia Bano, Tran N Chau, Megan L Sweet, Nicolaas C Baudoin, Andrew McCaffrey, Kai Fluet and 3 more

Abstract read
In one paragraph

Article in Cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Mathew BloomfieldDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0000-0002-1782-081X
Sydney M Huth *Department of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0009-0009-7105-8561
Daniella S McCausland *Department of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0009-0004-7718-8598
Ron SaadDepartment of Human Molecular Genetics and Biochemistry, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0009-0006-9483-8147
Nazia BanoTranslational Biology, Medicine, and Health program, Fralin Biomedical Research Institute, Virginia Tech, Roanoke, Virginia.ORCID 0009-0001-5759-5151
Tran N ChauDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0009-0007-2526-794X
Megan L SweetDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0000-0002-3718-7038
Nicolaas C BaudoinDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0000-0003-3316-5293
Andrew McCaffreyDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0009-0002-2143-6586
Kai FluetDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0009-0000-1584-3789
Eva M SchmelzDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.ORCID 0000-0002-3374-5266
Uri Ben-DavidDepartment of Human Molecular Genetics and Biochemistry, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.ORCID 0000-0001-7098-2378
Daniela CiminiDepartment of Biological Sciences and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, Virginia.ORCID 0000-0002-4082-4894

Funding

European Research Council (ERC) 945674National Cancer Institute (NCI) 1F31CA271763-01A1National Institute of General Medical Sciences (NIGMS) R01GM140042Tel Aviv University (TAU) Safra FellowshipVirginia Polytechnic Institute and State University (VT) Dean's Discovery Fund
6 · The paper itself

Abstract

Whole genome doubling (WGD) is a frequent event in cancer evolution associated with chromosomal instability, metastasis, and poor prognosis. Whereas the genomic consequences of WGD are well documented, nongenetic alterations that accompany WGD, such as changes to cell and nuclear size, may also play an important role in tetraploid (4N) cancer cell physiology. In this study, we showed that cell and nuclear volume does not always scale with DNA content after WGD in cancer cells, resulting in 4N cells that differ in size. Small size was associated with enhanced cell fitness, mitotic fidelity, and tumorigenicity in 4N cancer cells and with poor patient survival in WGD-positive human cancers. Overall, these results suggest that cell and nuclear size may contribute to the tumorigenic potential of 4N cancer cells and could be an important prognostic marker in human tumors that undergo WGD. SIGNIFICANCE: Cancer cell size varies after whole genome duplication, with smaller cells exhibiting high tumorigenicity and correlating with poor patient survival, demonstrating the clinical relevance and highlighting the biomarker potential of cell size.

Indexed as

CarcinogenesisCell NucleusCell Nucleus SizeChromosomal InstabilityNeoplasmsAnimalsCell Line, TumorCell SizeFemaleHumansMicePrognosisTetraploidy

Identifiers

PMID41570321
PMCPMC13136871

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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.