Evidence map›Paper›PMID 37537225›Full record

ArticleScientific reports2023

The crosstalking immune cells network creates a collective function beyond the function of each cellular constituent during the progression of hepatocellular carcinoma.

Nicholas Koelsch, Faridoddin Mirshahi, Hussein F Aqbi, Mulugeta Saneshaw, Michael O Idowu, Amy L Olex, Arun J Sanyal, Masoud H Manjili

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Anti-Tumour Immunity Relies on Targeting Tissue Homeostasis Through Monocyte-Driven Responses Rather Than Direct Tumour Cytotoxicity.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  6. Review
  7. Article
  8. Article
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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

8 authors at 5 institutions in 2 countries.

Nicholas KoelschDepartment of Microbiology & Immunology, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA. masoud.manjili@vcuhealth.org.
Faridoddin MirshahiDepartment of Internal Medicine, VCU School of Medicine, Richmond, VA, 23298, USA.
Hussein F AqbiCollege of Science, Mustansiriyah University, P.O. Box 14022, Baghdad, Iraq.
Mulugeta SaneshawDepartment of Internal Medicine, VCU School of Medicine, Richmond, VA, 23298, USA.
Michael O IdowuDepartment of Pathology, VCU School of Medicine, Richmond, VA, 23298, USA.
Amy L OlexC. Kenneth and Dianne Wright Center for Clinical and Translational Research, Virginia Commonwealth University School of Medicine, Richmond, USA.
Arun J SanyalDepartment of Internal Medicine, VCU School of Medicine, Richmond, VA, 23298, USA. koelschnj@vcu.edu.
Masoud H ManjiliDepartment of Microbiology & Immunology, Virginia Commonwealth University School of Medicine, Richmond, VA, 23298, USA. arun.sanyal@vcuhealth.org.
Children's Hospital of Richmond at VCU · USVirginia Commonwealth University · USMustansiriyah University · IQVCU Massey Comprehensive Cancer CenterVirginia Cancer Institute · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Renato Martins · 1985 to 2026
$51.0M
Research Supplement to Promote Diversity in Health Related ResearchUL1TR002649 · NCATS · VIRGINIA COMMONWEALTH UNIVERSITY · PI MOELLER, FREDERICK GERARD · 2018 to 2022
$19.1M
LIPIDOMICS BASED DIAGNOSTICS FOR NONALCOHOLIC STEATOHEPATITISR01DK105961 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENNIS, EDWARD A, SANYAL, ARUN J · 2015 to 2018
$2.8M
NCATS NIH HHS UL1 TR002649NCI NIH HHS P30 CA016059NIDDK NIH HHS R01 DK105961
6 · The paper itself

Abstract

Abundance of data on the role of inflammatory immune responses in the progression or inhibition of hepatocellular carcinoma (HCC) has failed to offer a curative immunotherapy for HCC. This is largely because of focusing on detailed specific cell types and missing the collective function of the hepatic immune system. To discover the collective immune function, we take systems immunology approach by performing high-throughput analysis of snRNAseq data collected from the liver of DIAMOND mice during the progression of nonalcoholic fatty liver disease (NAFLD) to HCC. We report that mutual signaling interactions of the hepatic immune cells in a dominant-subdominant manner, as well as their interaction with structural cells shape the immunological pattern manifesting a collective function beyond the function of the cellular constituents. Such pattern discovery approach recognized direct role of the innate immune cells in the progression of NASH and HCC. These data suggest that discovery of the immune pattern not only detects the immunological mechanism of HCC in spite of dynamic changes in immune cells during the course of disease but also offers immune modulatory interventions for the treatment of NAFLD and HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseAnimalsDisease ProgressionMice

Identifiers

PMID37537225
PMCPMC10400568
OpenAlexW4385555717

What OpenQuestion holds

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LicenceCC BY
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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.