Evidence map›Paper›PMID 25174820›Full record

ArticleMolecular medicine reports2014

Death receptor 5 expression is inversely correlated with prostate cancer progression.

Angeles Hernandez-Cueto, Daniel Hernandez-Cueto, Gabriela Antonio-Andres, Marisela Mendoza-Marin, Carlos Jimenez-Gutierrez, Ana Lilia Sandoval-Mejia, Rosario Mora-Campos, Cesar Gonzalez-Bonilla, Mario I Vega, Benjamin Bonavida and 1 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Angeles Hernandez-CuetoImmunology and Infection Research Unit, National Medical Center 'La Raza', IMSS, Mexico City 02200, Mexico.
Daniel Hernandez-CuetoOncology Disease Research Unit, Children Hospital of Mexico 'Federico Gomez', Mexico City 06720, Mexico.
Gabriela Antonio-AndresOncology Disease Research Unit, Children Hospital of Mexico 'Federico Gomez', Mexico City 06720, Mexico.
Marisela Mendoza-MarinDepartment of Pathology, Hospital General Regional No. 25, IMSS, Mexico City 06720, Mexico.
Carlos Jimenez-GutierrezWomen Hospital, Mexico City 11340, Mexico.
Ana Lilia Sandoval-MejiaGineco‑Obstetricia Hospital No. 3, CMN 'La Raza', IMSS, Mexico City 02200, Mexico.
Rosario Mora-CamposSpeciality Hospital CMN 'La Raza', IMSS, Mexico City 02200, Mexico.
Cesar Gonzalez-BonillaImmunology and Infection Research Unit, National Medical Center 'La Raza', IMSS, Mexico City 02200, Mexico.
Mario I VegaOncology Research Unit, Oncology Hospital, Siglo XXI National Medical Center, IMSS, Mexico City 06720, Mexico.
Benjamin BonavidaDepartment of Microbiology, Immunology and Molecular Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095, USA.
Sara Huerta-YepezOncology Disease Research Unit, Children Hospital of Mexico 'Federico Gomez', Mexico City 06720, Mexico.
Hospital Infantil de México Federico Gómez · MXCentro Medico Nacional Siglo XXI · MXMexican Social Security Institute · MXUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate carcinoma (PCa) is one of the most common cancers in men. Prostate-specific antigen (PSA) has been widely used to predict the outcome of PCa and screening with PSA has resulted in a decline in mortality. However, PSA is not an optimal prognostic tool as its sensitivity may be too low to reduce morbidity and mortality. Consequently, there is a demand for additional robust biomarkers for prostate cancer. Death receptor 5 (DR5) has been implicated in the prognosis of several cancers and it has been previously shown that it is negatively regulated by Yin Yang 1 (YY1) in prostate cancer cell lines. The present study investigated the clinical significance of DR5 expression in a prostate cancer patient cohort and its correlation with YY1 expression. Immunohistochemical analysis of protein expression distribution was performed using tissue microarray constructs from 54 primary PCa and 39 prostatic intraepithelial neoplasia (PIN) specimens. DR5 expression was dramatically reduced as a function of higher tumor grade. By contrast, YY1 expression was elevated in PCa tumors as compared with that in PIN, and was increased with higher tumor grade. DR5 had an inverse correlation with YY1 expression. Bioinformatic analyses corroborated these data. The present findings suggested that DR5 and YY1 expression levels may serve as progression biomarkers for prostate cancer.

Indexed as

Biomarkers, TumorDisease ProgressionGene ExpressionHumansMaleProstatic Intraepithelial NeoplasiaProstatic NeoplasmsReceptors, TNF-Related Apoptosis-Inducing LigandTissue Array AnalysisYY1 Transcription FactorBiomarkers, TumorReceptors, TNF-Related Apoptosis-Inducing LigandYY1 protein, humanYY1 Transcription Factor

Identifiers

PMID25174820
PMCPMC4214341
OpenAlexW2025777844

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.