Evidence map›Paper›PMID 26337081›Full record

ArticleOncotarget2015

Chromosomal catastrophe is a frequent event in clinically insignificant prostate cancer.

Irina V Kovtun, Stephen J Murphy, Sarah H Johnson, John C Cheville, George Vasmatzis

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  9. Review
  10. Integrated analysis of the genomic instability of PTEN in clinically insignificant and significant prostate cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2016
    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

5 authors at 2 institutions in 1 country.

Irina V KovtunDepartment of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.
Stephen J MurphyDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Sarah H JohnsonDepartment of Center of Individualized Medicine, Mayo Clinic, Rochester, Minnesota, USA.
John C ChevilleDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
George VasmatzisDepartment of Molecular Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Mayo Clinic · USWinnMed · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Massive genomic rearrangements, a result of single catastrophic event termed chromothrispsis or chromosomal catastrophe, have been identified in a variety of human cancers. In a few cancer types, chromothripsis was found to be associated with poor prognosis. We performed mate-pair sequencing and analysis of structural rearrangements in 132 prostate cancer cases which included clinically insignificant Gleason score 6 tumors, clinically significant tumors of higher grade (7+) and high grade prostatic intraepithelial neoplasia. Chromothripsis was observed at least 30 per cent of the samples across different grades. Surprisingly, it was frequently observed in clinically insignificant Gleason score 6 tumors, indicating that chromothripsis does not define more aggressive phenotype. The degree of chromothripsis did not increase significantly in tumors of advanced grades and did not appear to contribute to tumor progression. Our data showed that distribution of chromothriptic rearrangements differed from that of fragile sites but correlated with the size of chromosomes. We also provided evidence that rearrangements resulting from chromothripsis were present in the cells of neighboring Gleason patterns of the same tumor. Our data suggest that that chromothripsis plays role in prostate cancer initiation.

Indexed as

Chromosome AberrationsGene RearrangementBiomarkers, TumorChromosome Fragile SitesChromosomes, HumanDisease ProgressionDNA Copy Number VariationsGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHumansMaleNeoplasm GradingPhenotypeProstatic NeoplasmsTrans-ActivatorsTranscriptional Regulator ERGBiomarkers, TumorERG protein, humanTrans-ActivatorsTranscriptional Regulator ERGcatastrophechromothripsisgenomic rearrangementsGleason scoreprostate cancer

Identifiers

PMID26337081
PMCPMC4745713
OpenAlexW2116532769

What OpenQuestion holds

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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.