Evidence map›Paper›PMID 33034643›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2020

A bioengineered organotypic prostate model for the study of tumor microenvironment-induced immune cell activation.

Sheena C Kerr, Molly M Morgan, Amani A Gillette, Megan K Livingston, Karina M Lugo-Cintron, Peter F Favreau, Logan Florek, Brian P Johnson, Joshua M Lang, Melissa C Skala and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2020. 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
0.9field-weighted citation impact, top 23% 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, 18 citations in OpenAlex.

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  13. Immune cell mediated cabozantinib resistance for patients with renal cell carcinoma.Integrative biology : quantitative biosciences from nano to macro · 2021
    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

11 authors at 2 institutions in 1 country.

Sheena C KerrDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Molly M MorganDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Amani A GilletteDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, USA.
Megan K LivingstonDepartment of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
Karina M Lugo-CintronDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Peter F FavreauMorgridge Institute for Research, Madison, WI, USA.
Logan FlorekMorgridge Institute for Research, Madison, WI, USA.
Brian P JohnsonDepartment of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI, USA.
Joshua M LangCarbone Cancer Center, University of Wisconsin-Madison, Madison, WI, USA.
Melissa C SkalaCarbone Cancer Center, University of Wisconsin-Madison, Madison, WI, USA.
David J BeebeDepartment of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, WI, USA.
University of Wisconsin–Madison · USMorgridge Institute for Research · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
Microscale models of inflammation and its resolutionR01AI134749 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI BEEBE, DAVID J, HUTTENLOCHER, ANNA · 2018 to 2022
$3.8M
Optical imaging of pancreas cancer organoids for drug development and personalized treatmentR01CA211082 · NCI · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI SKALA, MELISSA CAROLINE · 2017 to 2021
$3.5M
An automated high-throughput tissue model for screening metastatic effectorsR01CA186134 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI BEEBE, DAVID J · 2015 to 2019
$3.1M
(PQ7) Quantitative in vivo optical imaging of tumor heterogeneityR01CA205101 · NCI · MORGRIDGE INSTITUTE FOR RESEARCH, INC. · PI SKALA, MELISSA CAROLINE · 2016 to 2020
$1.9M
Cellular-level Optical Metabolic Imaging to Predict Drug Response in CancerR01CA185747 · NCI · VANDERBILT UNIVERSITY · PI SKALA, MELISSA CAROLINE · 2014 to 2019
$1.6M
Area C: Functional microscale organotypic assays to predict patient response to anti-angiogenesis therapiesR33CA225281 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI ABEL, E JASON, BEEBE, DAVID J · 2017 to 2017
$1.5M
Elucidating AHR signaling interplay in orofacial clefting and endocrine disruption using microplate microfluidicsR00ES028744 · NIEHS · MICHIGAN STATE UNIVERSITY · PI JOHNSON, BRIAN P. · 2020 to 2022
$745k
Elucidating AHR signaling interplay in orofacial clefting and endocrine disruption using microplate microfluidicsK99ES028744 · NIEHS · UNIVERSITY OF WISCONSIN-MADISON · PI JOHNSON, BRIAN P. · 2018 to 2019
$200k
NCI NIH HHS L30 CA111079NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA185747NCI NIH HHS R01 CA186134NCI NIH HHS R01 CA205101NCI NIH HHS R01 CA211082NCI NIH HHS R33 CA225281NIAID NIH HHS R01 AI134749NIEHS NIH HHS K99 ES028744NIEHS NIH HHS R00 ES028744
6 · The paper itself

Abstract

The prostate tumor microenvironment (TME) is strongly immunosuppressive; it is largely driven by alteration in cell phenotypes (i.e. tumor-associated macrophages and exhausted cytotoxic T cells) that result in pro-tumorigenic conditions and tumor growth. A greater understanding into how these altered immune cell phenotypes are developed and could potentially be reversed would provide important insights into improved treatment efficacy for prostate cancer. Here, we report a microfluidic model of the prostate TME that mimics prostate ducts across various stages of prostate cancer progression, with associated stroma and immune cells. Using this platform, we exposed immune cells to a benign prostate TME or a metastatic prostate TME and investigated their metabolism, gene and cytokine expression. Immune cells exposed to the metastatic TME showed metabolic differences with a higher redox ratio indicating a switch to a more glycolytic metabolic profile. These cells also increased expression of pro-tumor response cytokines that have been shown to increase cell migration and angiogenesis such as Interleukin-1 (IL-1) a and Granulocyte-macrophage colony-stimulating factor (GM-CSF). Lastly, we observed decreased TLR, STAT signaling and TRAIL expression, suggesting that phenotypes derived from exposure to the metastatic TME could have an impaired anti-tumor response. This platform could provide a valuable tool for studying immune cell phenotypes in in vitro tumor microenvironments.

Indexed as

Immune SystemTumor MicroenvironmentCell MovementCell ProliferationCells, CulturedCytokinesFibroblastsGlycolysisGranulocyte-Macrophage Colony-Stimulating FactorHumansImmunosuppression TherapyIn Vitro TechniquesLeukocytes, MononuclearMaleMicrofluidicsModels, BiologicalCytokinesGranulocyte-Macrophage Colony-Stimulating FactorSTAT Transcription Factors

Identifiers

PMID33034643
PMCPMC7569006
OpenAlexW3092000181

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.