Evidence map›Paper›PMID 35418177›Full record

ArticleNature communications2022

Data-driven learning how oncogenic gene expression locally alters heterocellular networks.

David J Klinke, Audry Fernandez, Wentao Deng, Atefeh Razazan, Habibolla Latifizadeh, Anika C Pirkey

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. 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
0.6field-weighted citation impact, top 36% 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, 8 citations in OpenAlex.

  1. Article
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  5. Review
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

6 authors at 1 institution in 1 country.

David J KlinkeDepartment of Chemical and Biomedical Engineering, West Virginia University, Morgantown, WV, 26506, USA. david.klinke@mail.wvu.edu.ORCID 0000-0003-3299-4938
Audry FernandezDepartment of Microbiology, Immunology and Cell Biology, West Virginia University, Morgantown, WV, 26506, USA.
Wentao DengDepartment of Microbiology, Immunology and Cell Biology, West Virginia University, Morgantown, WV, 26506, USA.
Atefeh RazazanDepartment of Microbiology, Immunology and Cell Biology, West Virginia University, Morgantown, WV, 26506, USA.
Habibolla LatifizadehSchool of Mathematical and Data Sciences, West Virginia University, Morgantown, WV, 26506, USA.ORCID 0000-0002-5410-3094
Anika C PirkeyDepartment of Chemical and Biomedical Engineering, West Virginia University, Morgantown, WV, 26506, USA.ORCID 0000-0002-5349-3561
West Virginia University · US

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Sally Lynn Hodder · 2012 to 2026
$81.0M
WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI Travis Salisbury · 2012 to 2026
$61.1M
West Virginia Flow Cytometry Core FacilityP30GM103488 · NIGMS · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2012 to 2016
$4.8M
Integrative systems approach to identify local oncogenic modulation of the IL12 axisR01CA193473 · NCI · WEST VIRGINIA UNIVERSITY · PI KLINKE, DAVID JOHN · 2016 to 2020
$1.7M
COBRE FOR SIGNAL TRANSDUCTION AND CANCER PHASE IIIP30RR032138 · NCRR · WEST VIRGINIA UNIVERSITY · PI GIBSON, LAURA F. · 2011 to 2011
$1.1M
Special Becton Dickinson Fortessa Flow CytometerS10OD016165 · OD · WEST VIRGINIA UNIVERSITY · PI CUFF, CHRISTOPHER F · 2013 to 2013
$384k
NCI NIH HHS R01 CA193473NCRR NIH HHS P30 RR032138NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P30 GM103488NIGMS NIH HHS U54 GM104942NIH HHS S10 OD016165
6 · The paper itself

Abstract

Developing drugs increasingly relies on mechanistic modeling and simulation. Models that capture causal relations among genetic drivers of oncogenesis, functional plasticity, and host immunity complement wet experiments. Unfortunately, formulating such mechanistic cell-level models currently relies on hand curation, which can bias how data is interpreted or the priority of drug targets. In modeling molecular-level networks, rules and algorithms are employed to limit a priori biases in formulating mechanistic models. Here we combine digital cytometry with Bayesian network inference to generate causal models of cell-level networks linking an increase in gene expression associated with oncogenesis with alterations in stromal and immune cell subsets from bulk transcriptomic datasets. We predict how increased Cell Communication Network factor 4, a secreted matricellular protein, alters the tumor microenvironment using data from patients diagnosed with breast cancer and melanoma. Predictions are then tested using two immunocompetent mouse models for melanoma, which provide consistent experimental results.

Indexed as

AlgorithmsMelanomaAnimalsBayes TheoremCarcinogenesisGene Regulatory NetworksHumansMiceTranscriptomeTumor Microenvironment

Identifiers

PMID35418177
PMCPMC9007999
OpenAlexW4226094206

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.