Evidence map›Paper›PMID 38307951›Full record

ReviewNature reviews. Urology2024

The yin and yang of chromosomal instability in prostate cancer.

Marc Carceles-Cordon, Jacob J Orme, Josep Domingo-Domenech, Veronica Rodriguez-Bravo

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Urology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Loss of UFL1 drives chromosome instability and tumorigenesis of prostate cancer.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. 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 2 institutions in 1 country.

Marc Carceles-CordonDepartment of Urology, Mayo Clinic, Rochester, MN, USA.
Jacob J OrmeDepartment of Oncology, Mayo Clinic, Rochester, MN, USA.ORCID 0000-0002-0319-0239
Josep Domingo-DomenechDepartment of Urology, Mayo Clinic, Rochester, MN, USA. domingo-domenech.josep@mayo.edu.
Veronica Rodriguez-BravoDepartment of Urology, Mayo Clinic, Rochester, MN, USA. rodriguezbravo.veronica@mayo.edu.
Mayo Clinic · USMayo Clinic in Arizona · US

Funding

Determine the Microphthalmia Transcription Factor (MITF)-regulated cell rewiring mechanisms in lethal prostate cancerR01CA261925 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Josep Maria Domingo-Domenech · 2021 to 2026
$2.2M
Role of GATA2 signaling network in Lethal Prostate CancerR01CA207311 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DOMINGO-DOMENECH, JOSEP MARIA · 2016 to 2020
$2.2M
Role of Nuclear Pore-Regulated Mechanisms in Prostate Cancer AggressivenessR01CA237398 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RODRIGUEZ-BRAVO, VERONICA · 2020 to 2024
$2.0M
Mechanisms and therapeutic targeting of lethal prostate cancer master regulator transcription factorsR01CA280999 · NCI · MAYO CLINIC ROCHESTER · PI Josep Maria Domingo-Domenech, Veronica Rodriguez-Bravo · 2024 to 2026
$1.6M
NCI NIH HHS R01 CA207311NCI NIH HHS R01 CA237398NCI NIH HHS R01 CA261925NCI NIH HHS R01 CA280999
6 · The paper itself

Abstract

Metastatic prostate cancer remains an incurable lethal disease. Studies indicate that prostate cancer accumulates genomic changes during disease progression and displays the highest levels of chromosomal instability (CIN) across all types of metastatic tumours. CIN, which refers to ongoing chromosomal DNA gain or loss during mitosis, and derived aneuploidy, are known to be associated with increased tumour heterogeneity, metastasis and therapy resistance in many tumour types. Paradoxically, high CIN levels are also proposed to be detrimental to tumour cell survival, suggesting that cancer cells must develop adaptive mechanisms to ensure their survival. In the context of prostate cancer, studies indicate that CIN has a key role in disease progression and might also offer a therapeutic vulnerability that can be pharmacologically targeted. Thus, a comprehensive evaluation of the causes and consequences of CIN in prostate cancer, its contribution to aggressive advanced disease and a better understanding of the acquired CIN tolerance mechanisms can translate into new tumour classifications, biomarker development and therapeutic strategies.

Indexed as

Chromosomal InstabilityProstatic NeoplasmsDisease ProgressionHumansMale

Identifiers

PMID38307951
PMCPMC11156566
OpenAlexW4391486298

What OpenQuestion holds

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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.