Evidence map›Paper›PMID 25025847›Full record

ArticlePloS one2014

Lack of ephrin receptor A1 is a favorable independent prognostic factor in clear cell renal cell carcinoma.

Marieta I Toma, Kati Erdmann, Michael Diezel, Matthias Meinhardt, Stefan Zastrow, Susanne Fuessel, Manfred P Wirth, Gustavo B Baretton

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Optogenetic Regulation of EphA1 RTK Activation and Signaling.bioRxiv : the preprint server for biology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Eph/ephrin signaling in the kidney and lower urinary tract.Pediatric nephrology (Berlin, Germany) · 2016
    Review
  18. Article
  19. Article
  20. EphrinB2: Expression of a novel potential target in renal cell carcinoma.Indian journal of urology : IJU : journal of the Urological Society of India
    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

8 authors at 2 institutions in 1 country.

Marieta I TomaInstitute of Pathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Kati ErdmannDepartment of Urology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Michael DiezelInstitute of Pathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Matthias MeinhardtInstitute of Pathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Stefan ZastrowDepartment of Urology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Susanne FuesselDepartment of Urology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Manfred P WirthDepartment of Urology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Gustavo B BarettonInstitute of Pathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
TU Dresden · DEUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The EPH receptor tyrosine kinases and their cell-bound ligands, the ephrins, have been shown to be associated with cancer development and progression. In this study, mRNA and protein expression of the receptors EPHA1 and EPHA2 as well as of their ligand EFNA1 and their prognostic relevance in clear cell renal cell carcinoma was evaluated. Gene expression was measured in 75 cryo-preserved primary tumors and matched non-malignant renal specimens by quantitative PCR. Protein expression was analyzed by immunohistochemistry on tissue microarrays comprising non-malignant, primary tumors and metastatic renal tissues of 241 patients. Gene and protein expression of all three factors was altered in tumor specimens with EPHA1 and EPHA2 being generally diminished in tumors compared to normal renal tissue, whereas EFNA1 was commonly elevated. A positive EPHA1 and EPHA2 protein staining as well as a low EFNA1 protein level were significantly linked to more aggressive tumor features, but only a positive EPHA1 immunoreactivity was significantly associated with poor survival. In subgroup analyses, EPHA1 and EPHA2 protein levels were significantly higher in metastatic than in primary lesions. Patients with EPHA1/EPHA2-positive tumors or with tumors with positive EPHA1 and low EFNA1 immunoreactivity had the shortest survival rates compared to the respective other combinations. In a multivariate model, EPHA1 was an independent prognostic marker for different survival endpoints. In conclusion, an impaired EPH-ephrin signaling could contribute to the pathogenesis and progression of clear cell renal cell carcinoma.

Indexed as

AdultAgedAged, 80 and overBiomarkersCarcinoma, Renal CellDisease ProgressionEphrin-A1FemaleGene ExpressionHumansImmunohistochemistryKidney NeoplasmsMaleMiddle AgedNeoplasm GradingNeoplasm MetastasisBiomarkersEphrin-A1Receptor, EphA1Receptor, EphA2

Identifiers

PMID25025847
PMCPMC4099180
OpenAlexW1984339376

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.