Evidence map›Paper›PMID 18813347›Full record

ArticleNeoplasia (New York, N.Y.)2008

Decoy receptor 3 is a prognostic factor in renal cell cancer.

Stephan Macher-Goeppinger, Sebastian Aulmann, Nina Wagener, Benjamin Funke, Katrin E Tagscherer, Axel Haferkamp, Markus Hohenfellner, Sunghee Kim, Frank Autschbach, Peter Schirmacher and 1 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

35 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. CD15 Is a Risk Predictor and a Novel Target in Clear Cell Renal Cell Carcinoma.Pathobiology : journal of immunopathology, molecular and cellular biology · 2024
    Article
  3. Review
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  6. Case-Control Study onPharmacogenomics and personalized medicine · 2020
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  11. A functional polymorphism rs2257440 in the geneInternational journal of clinical and experimental pathology · 2017
    Article
  12. Article
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  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
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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

11 authors at 3 institutions in 1 country.

Stephan Macher-GoeppingerInstitute of Pathology, University of Heidelberg, Im Neuenheimer Feld 220, 69120 Heidelberg, Germany.
Sebastian Aulmann
Nina Wagener
Benjamin Funke
Katrin E Tagscherer
Axel Haferkamp
Markus Hohenfellner
Sunghee Kim
Frank Autschbach
Peter Schirmacher
Wilfried Roth
Heidelberg University · DEGerman Cancer Research Center · DENational Center for Tumor Diseases · DE

Funding

Decoy receptor 3 and liver cirrhosisR43DK076430 · NIDDK · BIOPOWERTECH · PI KIM, SUNGHEE · 2006 to 2006
$110k
Soluble Decoy Receptor 3 in Bacterial Infection and SepsisR43GM079070 · NIGMS · BIOPOWERTECH · PI KIM, SUNGHEE · 2006 to 2006
$107k
NIDDK NIH HHS DK076430NIDDK NIH HHS R43 DK076430NIGMS NIH HHS GM079070NIGMS NIH HHS R43 GM079070
6 · The paper itself

Abstract

backgroundDecoy receptor 3 (DcR3) is a soluble protein that binds to and inactivates the death ligand CD95L. Here, we studied a possible association between DcR3 expression and prognosis in patients with renal cell carcinomas (RCCs).

methodsA tissue microarray containing RCC tumor tissue samples and corresponding normal tissue samples was generated. Decoy receptor 3 expression in tumors of 560 patients was examined by immunohistochemistry. The effect of DcR3 expression on disease-specific survival and progression-free survival was assessed using univariate analysis and multivariate Cox regression analysis. Decoy receptor 3 serum levels were determined by ELISA.

findingsHigh DcR3 expression was associated with high-grade (P = .005) and high-stage (P = .048) RCCs. The incidence of distant metastasis (P = .03) and lymph node metastasis (P = .002) was significantly higher in the group with high DcR3 expression. Decoy receptor 3 expression correlated negatively with disease-specific survival (P < .001) and progression-free survival (P < .001) in univariate analyses. A multivariate Cox regression analysis retained DcR3 expression as an independent prognostic factor that outperformed the Karnofsky performance status. In patients with high-stage RCCs expressing DcR3, the 2-year survival probability was 25%, whereas in patients with DcR3-negative tumors, the survival probability was 65% (P < .001). Moreover, DcR3 serum levels were significantly higher in patients with high-stage localized disease (P = .007) and metastatic disease (P = .001).

interpretationDcR3 expression is an independent prognostic factor of RCC progression and mortality. Therefore, the assessment of DcR3 expression levels offers valuable prognostic information that could be used to select patients for adjuvant therapy studies.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, Renal CellCohort StudiesFemaleHumansIn Situ Hybridization, FluorescenceKidney NeoplasmsMaleMiddle AgedPrognosisReceptors, Tumor Necrosis Factor, Member 6bTissue Array AnalysisBiomarkers, TumorReceptors, Tumor Necrosis Factor, Member 6b

Identifiers

PMID18813347
PMCPMC2546583
OpenAlexW1273182181

What OpenQuestion holds

Textmetadata
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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.