Evidence map›Paper›PMID 27941872›Full record

ArticleOncogene2017

ER stress protein AGR2 precedes and is involved in the regulation of pancreatic cancer initiation.

L Dumartin, W Alrawashdeh, S M Trabulo, T P Radon, K Steiger, R M Feakins, M P di Magliano, C Heeschen, I Esposito, N R Lemoine and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 6% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 151 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

11 authors at 5 institutions in 3 countries.

L DumartinCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.
W AlrawashdehCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.
S M TrabuloCentre for Stem Cells in Cancer &Ageing, Barts Cancer Institute, Queen Mary University of London, London, UK.
T P RadonCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.
K SteigerInstitute of Pathology, Technische Universität München, Munich, Germany.
R M FeakinsDepartment of Histopathology, Royal London Hospital, London, UK.
M P di MaglianoDepartment of Surgery, Cell and Developmental Biology, University of Michigan, Ann Arbor, USA.
C HeeschenCentre for Stem Cells in Cancer &Ageing, Barts Cancer Institute, Queen Mary University of London, London, UK.
I EspositoInstitute of Pathology, Heinrich-Heine-University of Düsseldorf, Germany.
N R LemoineCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.
T Crnogorac-JurcevicCentre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.
Queen Mary University of London · GBHeinrich Heine University Düsseldorf · DERoyal London Hospital · GBTechnical University of Munich · DEUniversity of Michigan–Ann Arbor · US

Funding

Dosage-Dependent Hedgehog Signaling in Pancreatic CancerR01CA198074 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALLEN, BENJAMIN, PASCA DI MAGLIANO, MARINA · 2015 to 2019
$1.9M
Cancer Research UK 12008NCI NIH HHS R01 CA198074
6 · The paper itself

Abstract

The mechanisms of initiation of pancreatic ductal adenocarcinoma (PDAC) are still largely unknown. In the present study, we analysed the role of anterior gradient-2 (AGR2) in the earliest stages of pancreatic neoplasia. Immunohistochemical analysis of chronic pancreatitis (CP) and peritumoral areas in PDAC tissues showed that AGR2 was present in tubular complexes (TC) and early pancreatic intraepithelial neoplasia (PanINs). Moreover, AGR2 was also found in discrete subpopulations of non-transformed cells neighbouring these pre-neoplastic lesions. In primary cells derived from human patient-derived xenograft (PDX) model, flow-cytometry revealed that AGR2 was overexpressed in pancreatic cancer stem cells (CSC) compared with non-stem cancer cells. In LSL-Kras

Indexed as

AnimalsCarcinoma, Pancreatic DuctalCell Transformation, NeoplasticDisease Models, AnimalEndoplasmic Reticulum Chaperone BiPEndoplasmic Reticulum StressHumansMiceMucoproteinsOncogene ProteinsPancreatic NeoplasmsProto-Oncogene Proteins p21(ras)Agr2 protein, mouseEndoplasmic Reticulum Chaperone BiPHras protein, mouseHSPA5 protein, humanHspa5 protein, mouseMucoproteinsOncogene ProteinsProto-Oncogene Proteins p21(ras)

Identifiers

PMID27941872
PMCPMC5467015
OpenAlexW2566744224

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.