Evidence map›Paper›PMID 25157275›Full record

ArticleJournal of Cancer2014

Gene Expression Analysis of the 26S Proteasome Subunit PSMB4 Reveals Significant Upregulation, Different Expression and Association with Proliferation in Human Pulmonary Neuroendocrine Tumours.

Fabian Dominik Mairinger, Robert Fred Henry Walter, Dirk Theegarten, Thomas Hager, Claudia Vollbrecht, Daniel Christian Christoph, Karl Worm, Saskia Ting, Robert Werner, Georgios Stamatis and 9 more

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

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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

19 authors at 1 institution in 1 country.

Fabian Dominik Mairinger1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Robert Fred Henry Walter1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany. ; 2. Ruhrlandklinik, West German Lung Centre, University Hospital Essen, University of Duisburg-Essen, Germany.
Dirk Theegarten1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Thomas Hager1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Claudia Vollbrecht3. Institute of Pathology, University Hospital Cologne, University of Cologne, Germany.
Daniel Christian Christoph4. Department of Medical Oncology, University Hospital Essen, University of Duisburg-Essen, Germany.
Karl Worm1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Saskia Ting1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Robert Werner1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Georgios Stamatis5. Department of Thoracic Surgery, Ruhrlandklinik, West German Lung Centre, University Hospital Essen, University of Duisburg-Essen, Germany.
Thomas Mairinger6. Department of Pathology, Helios Klinikum Emil von Behring, Berlin, Germany.
Hideo Baba1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Konstantinos Zarogoulidis7. Pulmonary-Oncology, ``G. Papanikolaou`` General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Haidong Huang8. Department of Respiratory Diseases, Changhai Hospital/First Affiliated Hospital of the Second Military Medical University, Shanghai, People's Republic of China, China.
Qiang Li8. Department of Respiratory Diseases, Changhai Hospital/First Affiliated Hospital of the Second Military Medical University, Shanghai, People's Republic of China, China.
Kosmas Tsakiridis9. Thoracic Surgery Department, ``Saint Luke`` Private Clinic, Thessaloniki, Panorama, Greece.
Paul Zarogoulidis7. Pulmonary-Oncology, ``G. Papanikolaou`` General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Kurt Werner Schmid1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
Jeremias Wohlschlaeger1. Institute of Pathology, University Hospital Essen, University of Duisburg-Essen, Germany.
G. Papanikolaou General Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProteasomal subunit PSMB4 was suggested to be a survival gene in an animal model of hepatocellular carcinoma and in glioblastoma cell lines. In pulmonary adenocarcinoma, a high expression of these genes was found to be associated with poor differentiation and survival. This study investigates the gene expression levels of 26S proteasome subunits in human pulmonary neuroendocrine tumours including typical (TC) and atypical (AC) carcinoid tumours as well as small cell (SCLC) and large cell (LCNEC) neuroendocrine carcinomas. MATERIAL AND

methodsGene expression levels of proteasomal subunits (PSMA1, PSMA5, PSMB4, PSMB5 and PSMD1) were investigated in 80 neuroendocrine pulmonary tumours (each 20 TC, AC, LCNLC and SCLC) and compared to controls. mRNA levels were determined by using TaqMan assays. Immunohistochemistry on tissue microarrays (TMA) was performed to determine the expression of ki67, cleaved caspase 3 and PSMB4.

resultsAll proteasomal subunit gene expressions were significantly upregulated in TC, AC, SCLC and LCNEC compared to controls. PSMB4 mRNA is differently expressed between all neuroendocrine tumour subtypes demonstrating the highest expression and greatest range in LCNEC (p=0.043), and is significantly associated with proliferative activity (p=0.039).

conclusionIn line with other 26S proteasomal subunits PSMB4 is significantly increased, but differently expressed between pulmonary neuroendocrine tumours and is associated with the proliferative activity. Unlike in pulmonary adenocarcinomas, no association with biological behaviour was observed, suggesting that increased proteasomal subunit gene expression is a common and probably early event in the tumorigenesis of pulmonary neuroendocrine tumours regardless of their differentiation.

Indexed as

26S Proteasomecarcinoid tumoursneuroendocrine lung carcinoma.neuroendocrine lung tumoursTaqMan qPCR

Identifiers

PMID25157275
PMCPMC4142326
OpenAlexW2135937937

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.