Evidence map›Paper›PMID 27694890›Full record

ArticleNature cell biology2016

An interaction between Scribble and the NADPH oxidase complex controls M1 macrophage polarization and function.

Weiyue Zheng, Masataka Umitsu, Ishaan Jagan, Charles W Tran, Noboru Ishiyama, Michael BeGora, Kiyomi Araki, Pamela S Ohashi, Mitsuhiko Ikura, Senthil K Muthuswamy

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 70 citations in OpenAlex.

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  6. Metabolism, metabolites, and macrophages in cancer.Journal of hematology & oncology · 2023
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  12. An antisense circular RNA circSCRIB enhances cancer progression by suppressing parental gene splicing and translation.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

10 authors at 2 institutions in 2 countries.

Weiyue ZhengPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Masataka UmitsuPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Ishaan JaganPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Charles W TranPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.ORCID http://orcid.org/0000-0001-5818-818X
Noboru IshiyamaPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Michael BeGoraPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Kiyomi ArakiPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Pamela S OhashiPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Mitsuhiko IkuraPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
Senthil K MuthuswamyPrincess Margaret Cancer Center and Department of Medical Biophysics, University of Toronto, Toronto M5G 2M9, Canada.
University of Toronto · CABeth Israel Deaconess Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The polarity protein Scribble (SCRIB) regulates apical-basal polarity, directional migration and tumour suppression in Drosophila and mammals. Here we report that SCRIB is an important regulator of myeloid cell functions including bacterial infection and inflammation. SCRIB interacts directly with the NADPH oxidase (NOX) complex in a PSD95/Dlg/ZO-1 (PDZ)-domain-dependent manner and is required for NOX-induced reactive oxygen species (ROS) generation in culture and in vivo. On bacterial infection, SCRIB localized to phagosomes in a leucine-rich repeat-dependent manner and promoted ROS production within phagosomes to kill bacteria. Unexpectedly, SCRIB loss promoted M1 macrophage polarization and inflammation. Thus, SCRIB uncouples ROS-dependent bacterial killing activity from M1 polarization and inflammatory functions of macrophages. Modulating the SCRIB-NOX pathway can therefore identify ways to manage infection and inflammation with implications for chronic inflammatory diseases, sepsis and cancer.

Indexed as

AnimalsCell MembraneCell PolarityHumansInflammationIntracellular Signaling Peptides and ProteinsMacrophagesMembrane ProteinsMiceMyeloid CellsNADPH OxidasesPhagosomesReactive Oxygen SpeciesTumor Suppressor ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsNADPH OxidasesReactive Oxygen SpeciesSCRIB protein, humanscrib protein, mouseTumor Suppressor Proteins

Identifiers

PMID27694890
OpenAlexW2528883448

What OpenQuestion holds

Textmetadata
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.