Evidence map›Paper›PMID 28775934›Full record

ArticleAnalytical cellular pathology (Amsterdam)2017

Different Cytokine and Chemokine Expression Patterns in Malignant Compared to Those in Nonmalignant Renal Cells.

Nadine Gelbrich, Hannes Ahrend, Anne Kaul, Lars-Ove Brandenburg, Uwe Zimmermann, Alexander Mustea, Martin Burchardt, Denis Gümbel, Matthias B Stope

Open access · goldAbstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  4. Determination ofIn vivo (Athens, Greece)
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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

9 authors at 2 institutions in 1 country.

Nadine GelbrichDepartment of Urology, University Medicine Greifswald, Greifswald, Germany.
Hannes AhrendDepartment of Urology, University Medicine Greifswald, Greifswald, Germany.
Anne KaulDepartment of Gynaecology and Obstetrics, University Medicine Greifswald, Greifswald, Germany.
Lars-Ove BrandenburgDepartment of Anatomy and Cell Biology, RWTH Aachen University, Aachen, Germany.
Uwe ZimmermannDepartment of Urology, University Medicine Greifswald, Greifswald, Germany.
Alexander MusteaDepartment of Gynaecology and Obstetrics, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0002-3002-6039
Martin BurchardtDepartment of Urology, University Medicine Greifswald, Greifswald, Germany.
Denis GümbelDepartment of Trauma, Reconstructive Surgery and Rehabilitation Medicine, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0003-1330-2676
Matthias B StopeDepartment of Urology, University Medicine Greifswald, Greifswald, Germany.ORCID 0000-0003-4129-8854
Universitätsmedizin Greifswald · DERWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCytokines and chemokines are widely involved in cancer cell progression and thus represent promising candidate factors for new biomarkers.

methodsFour renal cell cancer (RCC) cell lines (Caki-1, 786-O, RCC4, and A498) and a nonmalignant renal cell line (RC-124) were examined with respect to their proliferation. The cytokine and chemokine expression pattern was examined by a DNA array (Human Cytokines & Chemokines RT

resultsCaki-1 and 786-O cells exhibited significantly increased proliferation rates, whereas RCC4 and A498 cells demonstrated attenuated proliferation, compared to nonmalignant RC-124 cells. Expression analysis revealed 52 cytokines and chemokines primarily involved in proliferation and inflammation and differentially expressed not only in malignant and nonmalignant renal cells but also in the four RCC cell lines.

conclusionThis is the first study examining the expression of 84 cytokines and chemokines in four RCC cell lines compared to that in a nonmalignant renal cell line. VEGFA, NODAL, and BMP6 correlated with RCC cell line proliferation and, thus, may represent putative clinical biomarkers for RCC progression as well as for RCC diagnosis and prognosis.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticCell Line, TumorCell ProliferationChemokinesHumansKidney NeoplasmsPrincipal Component AnalysisRNA, MessengerChemokinesRNA, Messenger

Identifiers

PMID28775934
PMCPMC5523453
OpenAlexW2730465718

What OpenQuestion holds

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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.