Evidence map›Paper›PMID 31683257›Full record

ArticleRedox biology2020

Inducible nitric oxide synthase-derived extracellular nitric oxide flux regulates proinflammatory responses at the single cell level.

Veena Somasundaram, Anne C Gilmore, Debashree Basudhar, Erika Mariana Palmieri, David A Scheiblin, William F Heinz, Robert Y S Cheng, Lisa A Ridnour, Grégoire Altan-Bonnet, Stephen J Lockett and 2 more

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 72 citations in OpenAlex.

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  9. Immune control of brain physiology.Nature reviews. Immunology · 2025
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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

12 authors at 3 institutions in 1 country.

Veena SomasundaramCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
Anne C GilmoreOptical Microscopy and Analysis Laboratory, Office of Science and Technology Resources, Center for Cancer Research, National Cancer Institute, USA.
Debashree BasudharCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
Erika Mariana PalmieriCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
David A ScheiblinOptical Microscopy and Analysis Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
William F HeinzOptical Microscopy and Analysis Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Robert Y S ChengCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
Lisa A RidnourCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
Grégoire Altan-BonnetCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
Stephen J LockettOptical Microscopy and Analysis Laboratory, Cancer Research Technology Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Daniel W McVicarCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA.
David A WinkCancer and Inflammation Program, Center for Cancer Research, National Cancer Institute, National Institute of Health, USA. Electronic address: wink@mail.nih.gov.
Center for Cancer Research · USNational Cancer Institute · USFrederick National Laboratory for Cancer Research · US

Funding

Signal Transduction of Paired Inhibitory Receptors of NK Cells and MacrophagesZIABC010300 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MCVICAR, DANIEL W. · 2009 to 2025
$24.6M
Nitric Oxide as a Modifier of Oxidative StressZIASC007281 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI WINK, DAVID · 2009 to 2025
$8.1M
Cytokine coordination of collective immune responses against tumorsZIABC011728 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI ALTAN-BONNET, GREGOIRE · 2016 to 2023
$3.7M
NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

The role of nitric oxide (NO) in cancer progression has largely been studied in the context of tumor NOS2 expression. However, pro- versus anti-tumor signaling is also affected by tumor cell-macrophage interactions. While these cell-cell interactions are partly regulated by NO, the functional effects of NO flux on proinflammatory (M1) macrophages are unknown. Using a triple negative murine breast cancer model, we explored the potential role of macrophage Nos2 on 4T1 tumor progression. The effects of NO on macrophage phenotype were examined in bone marrow derived macrophages from wild type and Nos2

Indexed as

AnimalsCell Line, TumorCyclooxygenase 2CytokinesDisease ProgressionFemaleGene Expression Regulation, NeoplasticLipopolysaccharidesMacrophagesMiceNeoplasm TransplantationNitric OxideNitric Oxide Synthase Type IISingle-Cell AnalysisTriple Negative Breast NeoplasmsCyclooxygenase 2CytokinesLipopolysaccharidesNitric OxideNitric Oxide Synthase Type IINos2 protein, mousePtgs2 protein, mouseMacrophageMetabolismNos2Tumor

Identifiers

PMID31683257
PMCPMC6920088
OpenAlexW2987914285

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.