Evidence map›Paper›PMID 30366420›Full record

ArticleCancers2018

Downregulation of TRAIL-Receptor 1 Increases TGFβ Type II Receptor Expression and TGFβ Signalling Via MicroRNA-370-3p in Pancreatic Cancer Cells.

David I Radke, Qi Ling, Robert Häsler, Gökhan Alp, Hendrik Ungefroren, Anna Trauzold

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 16 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

6 authors at 2 institutions in 2 countries.

David I RadkeInstitute for Experimental Cancer Research, University of Kiel, D-24105 Kiel, Germany. david.radke@gmx.de.
Qi LingInstitute for Experimental Cancer Research, University of Kiel, D-24105 Kiel, Germany. lingqi@zju.edu.cn.
Robert HäslerInstitute of Clinical Molecular Biology, University of Kiel, D-24105 Kiel, Germany. r.haesler@mucosa.de.ORCID 0000-0003-4174-8229
Gökhan AlpInstitute for Experimental Cancer Research, University of Kiel, D-24105 Kiel, Germany. alp77@gmx.de.
Hendrik UngefrorenClinic for General Surgery, Visceral, Thoracic, Transplantation and Pediatric Surgery, University Hospital Schleswig-Holstein, Campus Kiel, D-24105 Kiel, Germany. hendrik.ungefroren@uksh.de.
Anna TrauzoldInstitute for Experimental Cancer Research, University of Kiel, D-24105 Kiel, Germany. atrauzold@email.uni-kiel.de.
University Hospital Schleswig-Holstein · DEZhejiang University · CN

Funding

Deutsche Krebshilfe : doctoral stipend no. 110411
6 · The paper itself

Abstract

The accumulation of perturbations in signalling pathways resulting in an apoptosis-insensitive phenotype is largely responsible for the desperate prognosis of patients with pancreatic ductal adenocarcinoma (PDAC). Accumulating evidence suggests that the death receptors TRAIL-R1 and TRAIL-R2 play important roles in PDAC biology by acting as either tumour suppressors through induction of cell death or tumour promoters through induction of pro-inflammatory signalling, invasion and metastasis. TRAIL-R2 can also associate with nuclear proteins and alter the maturation of micro RNAs (miRs). By genome-wide miR profiling and quantitative PCR analyses we now demonstrate that knockdown of TRAIL-R1 in PDAC cells decreased the level of mature miR-370 and led to an increased abundance of the type II receptor for transforming growth factor β (TGFβ). Transfection of cells with an artificial miR-370-3p decreased the levels of TGFβ-RII. We further show that transient expression of the miR-370 mimic decreased TGFβ1-induced expression of

Indexed as

microRNApancreatic ductal adenocarcinomasignallingTGFβTGFβ receptor IITRAILTRAIL-receptor 1

Identifiers

PMID30366420
PMCPMC6267290
OpenAlexW2898506919

What OpenQuestion holds

Textmetadata
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.