Evidence map›Paper›PMID 37620309›Full record

ArticleCell death & disease2023

Expression of Cyclin E1 in hepatic stellate cells is critical for the induction and progression of liver fibrosis and hepatocellular carcinoma in mice.

Julia Otto, Anna Verwaayen, Christian Penners, Jana Hundertmark, Cheng Lin, Carina Kallen, Daniela Paffen, Tobias Otto, Hilmar Berger, Frank Tacke and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.5field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 32 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

16 authors at 5 institutions in 2 countries.

Julia OttoDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Anna Verwaayen *Department of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0001-9793-5862
Christian Penners *Department of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0002-4360-5785
Jana HundertmarkCharité - Universitätsmedizin Berlin, Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Campus Charité Mitte, Berlin, Germany.
Cheng LinDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Carina KallenDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Daniela PaffenDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Tobias OttoDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0001-5594-3055
Hilmar BergerCharité - Universitätsmedizin Berlin, Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Campus Charité Mitte, Berlin, Germany.
Frank TackeCharité - Universitätsmedizin Berlin, Department of Hepatology and Gastroenterology, Campus Virchow-Klinikum and Campus Charité Mitte, Berlin, Germany.
Ralf WeiskirchenInstitute of Molecular Pathobiochemistry, Experimental Gene Therapy and Clinical Chemistry (IFMPEGKC), University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0003-3888-0931
Yulia A NevzorovaDepartment of Immunology, Ophthalmology and ENT, Complutense University School of Medicine, Madrid, Spain.
Matthias BartneckDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0003-1516-9610
Christian TrautweinDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.ORCID 0000-0003-2762-8247
Roland SonntagDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany.
Christian LiedtkeDepartment of Medicine III, University Hospital RWTH Aachen, Aachen, Germany. cliedtke@ukaachen.de.ORCID 0000-0003-4681-7887
RWTH Aachen University · DECharité - Universitätsmedizin Berlin · DEDWI – Leibniz Institute for Interactive Materials · DEUniversidad Complutense de Madrid · ESUniversitätsklinikum Aachen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most severe malignancies with increasing incidence and limited treatment options. Typically, HCC develops during a multistep process involving chronic liver inflammation and liver fibrosis. The latter is characterized by the accumulation of extracellular matrix produced by Hepatic Stellate Cells (HSCs). This process involves cell cycle re-entry and proliferation of normally quiescent HSCs in an ordered sequence that is highly regulated by cyclins and associated cyclin-dependent kinases (CDKs) such as the Cyclin E1 (CCNE1)/CDK2 kinase complex. In the present study, we examined the role of Cyclin E1 (Ccne1) and Cdk2 genes in HSCs for liver fibrogenesis and hepatocarcinogenesis. To this end, we generated conditional knockout mice lacking Ccne1 or Cdk2 specifically in HSCs (Ccne1

Indexed as

Carcinoma, HepatocellularCyclin ELiver CirrhosisLiver NeoplasmsAnimalsCarcinogenesisHepatic Stellate CellsMiceOncogene ProteinsCyclin Ecyclin E1, mouseOncogene Proteins

Identifiers

PMID37620309
PMCPMC10449804
OpenAlexW4386140696

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.