Evidence map›Paper›PMID 31915468›Full record

ArticleDisease markers2019

Molecular Composition of Genomic

Manuela Krumbholz, Abbas Agaimy, Robert Stoehr, Maximilian Burger, Sven Wach, Helge Taubert, Bernd Wullich, Arndt Hartmann, Markus Metzler

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Disease markers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The Expression of Proto-OncogeneInternational journal of molecular sciences · 2022
    Review
  5. Review
  6. Article
  7. 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

9 authors at 2 institutions in 1 country.

Manuela KrumbholzDepartment of Pediatrics, University Hospital Erlangen, 91054 Erlangen, Germany.ORCID https://orcid.org/0000-0002-4416-0394
Abbas AgaimyDepartment of Pathology, University Hospital Erlangen, 91054 Erlangen, Germany.ORCID https://orcid.org/0000-0002-0445-8161
Robert StoehrDepartment of Pathology, University Hospital Erlangen, 91054 Erlangen, Germany.ORCID https://orcid.org/0000-0001-7018-3517
Maximilian BurgerDepartment of Urology, University of Regensburg, Caritas St. Josef Medical Center, 93053 Regensburg, Germany.
Sven WachDepartment of Urology and Pediatric Urology, University Hospital Erlangen, 91054 Erlangen, Germany.
Helge TaubertDepartment of Urology and Pediatric Urology, University Hospital Erlangen, 91054 Erlangen, Germany.ORCID https://orcid.org/0000-0002-9077-1727
Bernd WullichDepartment of Urology and Pediatric Urology, University Hospital Erlangen, 91054 Erlangen, Germany.
Arndt HartmannDepartment of Pathology, University Hospital Erlangen, 91054 Erlangen, Germany.
Markus MetzlerDepartment of Pediatrics, University Hospital Erlangen, 91054 Erlangen, Germany.
Universitätsklinikum Erlangen · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is increasing interest in the use of cell-free circulating tumor DNA (ctDNA) as a serum marker for therapy assessment in prostate cancer patients. Prostate cancer is characterized by relatively low numbers of mutations, and, in contrast to many other common epithelial cancers, commercially available single nucleotide mutation assays for quantification of ctDNA are insufficient for therapy assessment in this disease. However, prostate cancer shares some similarity with translocation-affected mesenchymal tumors (e.g., leukemia and Ewing sarcoma), which are common in pediatric oncology, where chromosomal translocations are used as biomarkers for quantification of the tumor burden. Approximately 50% of prostate cancers carry a chromosomal translocation resulting in generation of the

Indexed as

AgedBiomarkers, TumorCell-Free Nucleic AcidsCell Line, TumorChildHumansMaleMiddle AgedNeoplasms, Connective and Soft TissueOncogene Proteins, FusionPrecision MedicineProstatic NeoplasmsRepetitive Sequences, Nucleic AcidBiomarkers, TumorCell-Free Nucleic AcidsOncogene Proteins, FusionTMPRSS2-ERG fusion protein, human

Identifiers

PMID31915468
PMCPMC6930771
OpenAlexW2996698457

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.