Evidence map›Paper›PMID 31546614›Full record

ArticleCancers2019

An IKK/NF-κB Activation/p53 Deletion Sequence Drives Liver Carcinogenesis and Tumor Differentiation.

Michael Svinarenko, Sarah-Fee Katz, Umesh Tharehalli, Medhanie A Mulaw, Harald J Maier, Yoshiaki Sunami, Sarah K Fischer, Yuexin Chen, Sabine Heurich, Lena Erkert and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 50% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
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

15 authors at 5 institutions in 1 country.

Michael SvinarenkoDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. michael.svinarenko@uni-ulm.de.
Sarah-Fee KatzDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. sarah-fee.katz@web.de.
Umesh TharehalliDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. umesh.tharehalli@uni-ulm.de.ORCID 0000-0002-4907-5017
Medhanie A MulawInstitute of Experimental Cancer Research, Comprehensive Cancer Center Ulm, University Hospital Ulm, 89081 Ulm, Germany. medhanie.mulaw@uni-ulm.de.
Harald J MaierDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. maierhj@gmail.com.
Yoshiaki SunamiDepartment of Visceral, Vascular and Endocrine Surgery, Halle University Hospital, Martin-Luther University Halle-Wittenberg, 06120 Halle, Germany. yoshiaki.sunami@uk-halle.de.ORCID 0000-0002-1235-7512
Sarah K FischerDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. sarah.k.f.91@googlemail.com.
Yuexin ChenDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. yuexin.chen@tum.de.
Sabine HeurichDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. sabine.heurich@uni-ulm.de.
Lena ErkertDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. lena.erkert@t-online.de.
Andrea TannapfelInstitute of Pathology, Ruhr University Bochum, 44789 Bochum, Germany. andrea.tannapfel@pathologie-bochum.de.
Thomas WirthInstitute of Physiological Chemistry, Ulm University, 89081 Ulm, Germany. thomas.wirth@uni-ulm.de.
Reinhold SchirmbeckDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. Reinhold.Schirmbeck@uniklinik-ulm.de.
Thomas SeufferleinDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. Thomas.Seufferlein@uniklinik-ulm.de.
André LechelDepartment of Internal Medicine I, University Hospital Ulm, 89081 Ulm, Germany. andre.lechel@uni-ulm.de.ORCID 0000-0003-0221-6959
University Hospital Ulm · DEUniversität Ulm · DEMartin Luther University Halle-Wittenberg · DERuhr University Bochum · DETUM Klinikum · DE

Funding

Deutsche Forschungsgemeinschaft GRK2254/C3-HEISTDeutsche Krebshilfe 111264
6 · The paper itself

Abstract

backgroundMost liver tumors arise on the basis of chronic liver diseases that trigger inflammatory responses. Besides inflammation, subsequent defects in the p53-signaling pathway frequently occurs in liver cancer. In this study, we analyzed the consequences of inflammation and p53 loss in liver carcinogenesis.

methodsWe used inducible liver-specific transgenic mouse strains to analyze the consequences of NF-κB/p65 activation mimicking chronic inflammation and subsequent p53 loss.

results

conclusionsIn conclusion, activation of NF-κB/p65 mimicking chronic inflammation provokes the formation of liver carcinoma. Collateral disruption of

Indexed as

ectopic lymphoid structureshepatocellular carcinomainflammationintrahepatic cholangiocarcinomaprogenitor cells

Identifiers

PMID31546614
PMCPMC6827060
OpenAlexW2973348529

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.