Evidence map›Paper›PMID 31382615›Full record

ArticleNutrients2019

Identification of the Secreted Proteins Originated from Primary Human Hepatocytes and HepG2 Cells.

Andras Franko, Sonja Hartwig, Jörg Kotzka, Marc Ruoß, Andreas K Nüssler, Alfred Königsrainer, Hans-Ulrich Häring, Stefan Lehr, Andreas Peter

Open access · goldAbstract readComparative Study
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  6. Cgref1 is a CREB-H-regulated hepatokine that promotes hepaticInternational journal of biological sciences · 2025
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  18. Z-αScience advances · 2022
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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

9 authors at 3 institutions in 1 country.

Andras FrankoDepartment for Diagnostic Laboratory Medicine, Institute for Clinical Chemistry and Pathobiochemistry, University Hospital Tübingen, 72076 Tübingen, Germany. andras.franko@med.uni-tuebingen.de.ORCID 0000-0003-0485-5439
Sonja HartwigGerman Center for Diabetes Research (DZD e.V.), 85764 Neuherberg, Germany.
Jörg KotzkaGerman Center for Diabetes Research (DZD e.V.), 85764 Neuherberg, Germany.ORCID 0000-0003-1173-9372
Marc RuoßDepartment of Traumatology, BG Trauma Clinic, Siegfried Weller Institute for Trauma Research, Eberhard Karls Universität Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-0193-4425
Andreas K NüsslerDepartment of Traumatology, BG Trauma Clinic, Siegfried Weller Institute for Trauma Research, Eberhard Karls Universität Tübingen, 72076 Tübingen, Germany.
Alfred KönigsrainerDepartment of General, Visceral and Transplant Surgery, University Hospital Tübingen, 72076 Tübingen, Germany.
Hans-Ulrich HäringInstitute for Diabetes Research and Metabolic Diseases of the Helmholtz Centre Munich, University of Tübingen, 72076 Tübingen, Germany.
Stefan LehrGerman Center for Diabetes Research (DZD e.V.), 85764 Neuherberg, Germany.
Andreas PeterDepartment for Diagnostic Laboratory Medicine, Institute for Clinical Chemistry and Pathobiochemistry, University Hospital Tübingen, 72076 Tübingen, Germany.
Deutsches Diabetes-Zentrum e.V. · DEUniversity of Tübingen · DEUniversity Children's Hospital Tübingen · DE

Funding

German Center for Diabetes Research (DZD e.V.)
6 · The paper itself

Abstract

The liver plays a pivotal role in whole-body carbohydrate, lipid, and protein metabolism. One of the key regulators of glucose and lipid metabolism are hepatokines, which are found among the liver secreted proteins, defined as liver secretome. To elucidate the composition of the human liver secretome and identify hepatokines in primary human hepatocytes (PHH), we conducted comprehensive protein profiling on conditioned medium (CM) of PHH. Secretome profiling using liquid chromatography-electrospray ionization tandem mass spectrometry (LC-MS/MS) identified 691 potential hepatokines in PHH. Subsequently, pathway analysis assigned these proteins to acute phase response, coagulation, and complement system pathways. The secretome of PHH was compared to the secreted proteins of the liver hepatoma cell line HepG2. Although the secretome of PHH and HepG2 cells show a high overlap, the HepG2 secretome rather mirrors the fetal liver with some cancer characteristics. Collectively, our study represents one of the most comprehensive secretome profiling approaches for PHH, allowing new insights into the composition of the secretome derived from primary human material, and points out strength and weakness of using HepG2 cell secretome as a model for the analysis of the human liver secretome.

Indexed as

Chromatography, Reverse-PhaseHepatocytesHep G2 CellsHumansPrimary Cell CultureProteinsProteomicsSecretory PathwaySpectrometry, Mass, Electrospray IonizationTandem Mass SpectrometryProteinshepatokinesHepG2 cellsmass spectrometryprimary human hepatocytesproteomics

Identifiers

PMID31382615
PMCPMC6723870
OpenAlexW2966857034

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.