Evidence map›Paper›PMID 23584885›Full record

ArticleArchives of gynecology and obstetrics2013

Membrane expression of TRAIL receptors DR4, DR5, DcR1 and DcR2 in the normal endometrium, atypical endometrial hyperplasia and endometrioid adenocarcinoma: a tissue microarray study.

Leszek Gottwald, Janusz Piekarski, Robert Kubiak, Jarosław Szwalski, Grażyna Pasz-Walczak, Piotr Sęk, Michał Spych, Jacek Suzin, Wiesław Tyliński, Arkadiusz Jeziorski

Open access · hybridAbstract read
In one paragraph

Article in Archives of gynecology and obstetrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. 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

10 authors at 2 institutions in 2 countries.

Leszek GottwaldDepartment of Radiotherapy, Medical University of Lodz, ul Paderewskiego 4, 93-509, Lodz, Poland, lgottwald@wp.pl.
Janusz Piekarski
Robert Kubiak
Jarosław Szwalski
Grażyna Pasz-Walczak
Piotr Sęk
Michał Spych
Jacek Suzin
Wiesław Tyliński
Arkadiusz Jeziorski
Medical University of Lodz · PLOlympus (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate the membrane expression of DR4, DR5, DcR1 and DcR2 in the normal endometrium (NE), atypical endometrial hyperplasia (AEH) and endometrioid adenocarcinoma (EAC).

methodsThe study comprised 197 patients: 20 NE, 18 AEH and 159 EAC. Tissue microarrays were constructed. Membrane expression of DR4, DR5, DcR1 and DcR2 was examined and presented as total score (TS).

resultsIn EAC, the membrane expression of DR4, DR5 and DcR2 was less common compared to NE (p < 0.001; p < 0.001; p = 0.018) and AEH (p < 0.001; p < 0.001; p = 0.004). In EAC the membrane expression of DcR1 did not differ when compared to NE (p = 0.055) and AEH (p = 0.173). A strong correlation was found between the type of endometrial tissue (NE/AEH/EAC) and the TS of DR4 (p < 0.001), DR5 (p < 0.001), DcR1 (p = 0.033) and DcR2 (p < 0.001). In EAC, the TS of DR4, DR5, DcR1 and DcR2 was not related to grading and staging. In EAC, the membrane expression of DR5, but not DR4, DcR1 and DcR2, was related to better disease-free survival (DFS). The overall survival (OS) was not related to membrane TRAIL receptors expression.

conclusionsThe membrane expression of the receptors for TRAIL DR4, DR5, DcR1 and DcR2 is greater in NE than EAC. The level of membrane staining of the receptors in EAC is not dependent on grading and staging. In EAC patients, membrane expression of DR4, DR5, DcR1 and DcR2 are not independent predictors of survival.

Indexed as

BiomarkersBiomarkers, TumorCarcinoma, EndometrioidCell MembraneEndometrial HyperplasiaEndometrial NeoplasmsEndometriumFemaleGPI-Linked ProteinsHumansImmunohistochemistryReceptors, TNF-Related Apoptosis-Inducing LigandReceptors, Tumor Necrosis Factor, Member 10cSurvival AnalysisTissue Array AnalysisTumor Necrosis Factor Decoy ReceptorsBiomarkersBiomarkers, TumorGPI-Linked ProteinsReceptors, TNF-Related Apoptosis-Inducing LigandReceptors, Tumor Necrosis Factor, Member 10cTNFRSF10A protein, humanTNFRSF10C protein, humanTNFRSF10D protein, humanTumor Necrosis Factor Decoy Receptors

Identifiers

PMID23584885
PMCPMC3778234
OpenAlexW2002149299

What OpenQuestion holds

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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.