Evidence map›Paper›PMID 37778926›Full record

ReviewTrends in genetics : TIG2023

Aneuploidy in human cancer: new tools and perspectives.

Asad A Lakhani, Sarah L Thompson, Jason M Sheltzer

Open access · greenAbstract readReview
In one paragraph

Review in Trends in genetics : TIG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
7.2field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Investigating the Consequences of Aneuploidy in Cancer and Normal Tissue.Advances in experimental medicine and biology · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. The Hallmarks of Aneuploidy in Cancer and Congenital Syndromes.Annual review of genomics and human genetics · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. The two sides of chromosomal instability: drivers and brakes in cancer.Signal transduction and targeted therapy · 2024
    Review
  16. Review
  17. Review
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

3 authors at 2 institutions in 1 country.

Asad A LakhaniCold Spring Harbor Laboratory School of Biological Sciences, Cold Spring, Harbor, NY 11724, USA.
Sarah L ThompsonYale University School of Medicine, New Haven, CT 06511, USA.
Jason M SheltzerYale University School of Medicine, New Haven, CT 06511, USA. Electronic address: Jason.Sheltzer@yale.edu.
Yale University · USCold Spring Harbor Laboratory · US

Funding

Genomic and functional approaches to characterize Chr1q gains in cancerR01CA276666 · NCI · YALE UNIVERSITY · PI Jason Sheltzer, Ruping Sun · 2023 to 2026
$2.4M
Discovering the mechanisms-of-action of mistargeted anti-cancer agentsR01CA237652 · NCI · YALE UNIVERSITY · PI SHELTZER, JASON · 2020 to 2024
$1.6M
NCI NIH HHS R01 CA237652NCI NIH HHS R01 CA276666
6 · The paper itself

Abstract

Chromosome copy number imbalances, otherwise known as aneuploidies, are a common but poorly understood feature of cancer. Here, we describe recent advances in both detecting and manipulating aneuploidies that have greatly advanced our ability to study their role in tumorigenesis. In particular, new clustered regularly interspaced short palindromic repeats (CRISPR)-based techniques have been developed that allow the creation of isogenic cell lines with specific chromosomal changes, thereby facilitating experiments in genetically controlled backgrounds to uncover the consequences of aneuploidy. These approaches provide increasing evidence that aneuploidy is a key driver of cancer development and enable the identification of multiple dosage-sensitive genes encoded on aneuploid chromosomes. Consequently, measuring aneuploidy may inform clinical prognosis, while treatment strategies that target aneuploidy could represent a novel method to counter malignant growth.

Indexed as

AneuploidyNeoplasmsHumansaneuploidychromosome engineeringdosage-sensitive genessomatic copy number alterations

Identifiers

PMID37778926
PMCPMC10715718
OpenAlexW4387190854

What OpenQuestion holds

Textmetadata
LicenceTDM
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.