Evidence map›Paper›PMID 29429965›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Mast cells promote small bowel cancer in a tumor stage-specific and cytokine-dependent manner.

Abdulrahman M Saadalla, Abu Osman, Michael F Gurish, Kristen L Dennis, Nichole R Blatner, Abdulmohammad Pezeshki, Kelly M McNagny, Hilde Cheroutre, Fotini Gounari, Khashayarsha Khazaie

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 47 citations in OpenAlex.

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  16. IL-9 and IL-9-producing cells in tumor immunity.Cell communication and signaling : CCS · 2020
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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 6 institutions in 2 countries.

Abdulrahman M SaadallaDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Abu OsmanDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Michael F GurishDivision of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Kristen L DennisRobert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.
Nichole R BlatnerRobert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611.
Abdulmohammad PezeshkiDepartment of Immunology, Mayo Clinic, Rochester, MN 55905.
Kelly M McNagnyThe Biomedical Research Centre, University of British Columbia, Vancouver, BC, V6T 1Z3 Canada.ORCID 0000-0003-4737-3499
Hilde CheroutreLa Jolla Institute of Allergy and Immunology, San Diego, CA 92121.
Fotini GounariKnapp Center for Lupus Research, Section of Rheumatology, Department of Medicine, University of Chicago, Chicago, IL 60637.
Khashayarsha KhazaieDepartment of Immunology, Mayo Clinic, Rochester, MN 55905; khazaie@mayo.edu.ORCID 0000-0002-7884-1817
Mayo Clinic in Arizona · USNorthwestern University · USBrigham and Women's Hospital · USLa Jolla Institute for Immunology · USUniversity of British Columbia · CAUniversity of Chicago · US

Funding

How beta-catenin expands Foxp3+RORgammat+ Pro-inflammatoryT-regulatory cells - RenewalR01AI108682 · NIAID · UNIVERSITY OF CHICAGO · PI GOUNARI, FOTINI, KHAZAIE, KHASHAYARSHA · 2014 to 2024
$5.1M
Proinflammatory T Regulatory Cells in Colon CancerR01CA160436 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI KHAZAIE, KHASHAYARSHA · 2012 to 2017
$2.0M
NCI NIH HHS R01 CA160436NIAID NIH HHS R01 AI108682
6 · The paper itself

Abstract

Mast cells (MCs) are tissue resident sentinels that mature and orchestrate inflammation in response to infection and allergy. While they are also frequently observed in tumors, the contribution of MCs to carcinogenesis remains unclear. Here, we show that sequential oncogenic events in gut epithelia expand different types of MCs in a temporal-, spatial-, and cytokine-dependent manner. The first wave of MCs expands focally in benign adenomatous polyps, which have elevated levels of IL-10, IL-13, and IL-33, and are rich in type-2 innate lymphoid cells (ILC2s). These vanguard MCs adhere to the transformed epithelial cells and express murine mast cell protease 2 (mMCP2; a typical mucosal MC protease) and, to a lesser extent, the connective tissue mast cell (CTMC) protease mMCP6. Persistence of MCs is strictly dependent on T cell-derived IL-10, and their loss in the absence of IL-10-expressing T cells markedly delays small bowel (SB) polyposis. MCs expand profusely in polyposis-prone mice when T cells overexpress IL-10. The frequency of polyp-associated MCs is unaltered in response to broad-spectrum antibiotics, arguing against a microbial component driving their recruitment. Intriguingly, when polyps become invasive, a second wave of mMCP5

Indexed as

AnimalsCells, CulturedChymasesCytokinesIntestinal NeoplasmsIntestine, SmallLymphocytesMast CellsMiceMucous MembraneNeoplasm Stagingchymase 2ChymasesCytokinescancerILC2inflammationmast cellssmall bowel

Identifiers

PMID29429965
PMCPMC5816178
OpenAlexW2791578161

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.