Evidence map›Paper›PMID 31636296›Full record

ArticleScientific reports2019

Computational/experimental evaluation of liver metastasis post hepatic injury: interactions with macrophages and transitional ECM.

Shanice V Hudson, Hunter A Miller, Grace E Mahlbacher, Douglas Saforo, Levi J Beverly, Gavin E Arteel, Hermann B Frieboes

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
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  7. Article
  8. Article
  9. The liver matrisome - looking beyond collagens.JHEP reports : innovation in hepatology · 2020
    Review
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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

7 authors at 1 institution in 1 country.

Shanice V HudsonDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, 40292, USA.
Hunter A MillerDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, 40292, USA.
Grace E MahlbacherDepartment of Bioengineering, University of Louisville, Louisville, KY, 40292, USA.
Douglas SaforoDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, 40292, USA.
Levi J BeverlyDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, 40292, USA.
Gavin E ArteelDepartment of Medicine, Division of Gastroenterology, Hepatology, and Nutrition, University of Pittsburgh, Pittsburgh, PA, 15261, USA.
Hermann B FrieboesDepartment of Pharmacology and Toxicology, University of Louisville, Louisville, KY, 40292, USA. hbfrie01@louisville.edu.ORCID http://orcid.org/0000-0001-5959-4286
University of Louisville · US

Funding

Pittsburgh Liver Research CenterP30DK120531 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DAVID A GELLER · 2019 to 2026
$10.9M
Role of ECM and inflammatory remodeling in alcohol-induced liver and lung damage-diversity supplementR01AA021978 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ARTEEL, GAVIN E · 2014 to 2018
$1.8M
Integrated framework to predict chemotherapy response post lung tumor resectionR15CA203605 · NCI · UNIVERSITY OF LOUISVILLE · PI FRIEBOES, HERMANN · 2016 to 2016
$462k
NCI NIH HHS R15 CA203605NIAAA NIH HHS R01 AA021978NIDDK NIH HHS P30 DK120531U.S. Department of Health & Human Services | National Institutes of Health (NIH) R15CA203605
6 · The paper itself

Abstract

The complex interactions between subclinical changes to hepatic extracellular matrix (ECM) in response to injury and tumor-associated macrophage microenvironmental cues facilitating metastatic cell seeding remain poorly understood. This study implements a combined computational modeling and experimental approach to evaluate tumor growth following hepatic injury, focusing on ECM remodeling and interactions with local macrophages. Experiments were performed to determine ECM density and macrophage-associated cytokine levels. Effects of ECM remodeling along with macrophage polarization on tumor growth were evaluated via computational modeling. For primary or metastatic cells in co-culture with macrophages, TNF-α levels were 5× higher with M1 vs. M2 macrophages. Metastatic cell co-culture exhibited 10× higher TNF-α induction than with primary tumor cells. Although TGFβ1 induction was similar between both co-cultures, levels were slightly higher with primary cells in the presence of M1. Simulated metastatic tumors exhibited decreased growth compared to primary tumors, due to high local M1-induced cytotoxicity, even in a highly vascularized microenvironment. Experimental analysis combined with computational modeling may provide insight into interactions between ECM remodeling, macrophage polarization, and liver tumor growth.

Indexed as

Computer SimulationAnimalsCell DifferentiationCell Line, TumorCell MovementCell ProliferationExtracellular MatrixFemaleLiverLiver NeoplasmsMacrophagesMaleMice, Inbred C57BLNeovascularization, PhysiologicTransforming Growth Factor beta1Tumor BurdenTransforming Growth Factor beta1Tumor Necrosis Factor-alpha

Identifiers

PMID31636296
PMCPMC6803648
OpenAlexW2980578372

What OpenQuestion holds

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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.