Evidence map›Paper›PMID 32251323›Full record

ArticleScientific reports2020

Differential impact of the ERBB receptors EGFR and ERBB2 on the initiation of precursor lesions of pancreatic ductal adenocarcinoma.

Nora Meyers, Claude Gérard, Frédéric P Lemaigre, Patrick Jacquemin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 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

4 authors at 1 institution in 1 country.

Nora Meyers *Université catholique de Louvain, de Duve Institute, Brussels, Belgium.
Claude Gérard *Université catholique de Louvain, de Duve Institute, Brussels, Belgium.
Frédéric P LemaigreUniversité catholique de Louvain, de Duve Institute, Brussels, Belgium. frederic.lemaigre@uclouvain.be.
Patrick JacqueminUniversité catholique de Louvain, de Duve Institute, Brussels, Belgium. patrick.jacquemin@uclouvain.be.
de Duve Institute · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Earlier diagnosis of pancreatic ductal adenocarcinoma (PDAC) requires better understanding of the mechanisms driving tumorigenesis. In this context, depletion of Epidermal Growth Factor Receptor (EGFR) is known to impair development of PDAC-initiating lesions called acinar-to-ductal metaplasia (ADM) and Pancreatic Intraepithelial Neoplasia (PanIN). In contrast, the role of v-erb-b2 erythroblastic leukemia viral oncogene homolog 2 (ERBB2), the preferred dimerization partner of EGFR, remains poorly understood. Here, using a mouse model with inactivation of Erbb2 in pancreatic acinar cells, we found that Erbb2 is dispensable for inflammation- and KRas

Indexed as

Acinar CellsAnimalsCarcinoma, Pancreatic DuctalErb-b2 Receptor Tyrosine KinasesErbB ReceptorsGene Expression Regulation, NeoplasticHumansMice, Mutant StrainsMice, TransgenicModels, TheoreticalPancreatic NeoplasmsSignal TransductionEGFR protein, humanEGFR protein, mouseERBB2 protein, humanErbb2 protein, mouseErb-b2 Receptor Tyrosine KinasesErbB Receptors

Identifiers

PMID32251323
PMCPMC7090067
OpenAlexW3012575245

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.