Evidence map›Paper›PMID 32921956›Full record

ArticleWorld journal of gastroenterology2020

Immune and microRNA responses to

Rasha Raheem Alkarkoushi, Yvonne Hui, Abbas S Tavakoli, Udai Singh, Prakash Nagarkatti, Mitzi Nagarkatti, Ioulia Chatzistamou, Marpe Bam, Traci L Testerman

Open access · greenAbstract read
In one paragraph

Article in World journal of gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Rasha Raheem AlkarkoushiDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Yvonne HuiDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Abbas S TavakoliCollege of Nursing, University of South Carolina, University of South Carolina, Columbia, SC 29208, United States.
Udai SinghDepartment of Medicine, Hematology and Oncology, University of Virginia School of Medicine, Charlottesville, VA 22908, United States.
Prakash NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Mitzi NagarkattiDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Ioulia ChatzistamouDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Marpe BamDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States.
Traci L TestermanDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, SC 29209, United States. traci.testerman@uscmed.sc.edu.
University of South Carolina · US

Funding

Targeting early ceramide elevation in pre-symptomatic eczemaP20GM103641 · NIGMS · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ENOS, REILLY, NAGARKATTI, PRAKASH S · 2012 to 2023
$20.7M
AhR ligands in epigenetic dysregulation of T cellsR01AI123947 · NIAID · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, MITZI, NAGARKATTI, PRAKASH S · 2017 to 2021
$1.8M
NIAID NIH HHS R01 AI123947NIGMS NIH HHS P20 GM103641
6 · The paper itself

Abstract

backgroundIndole-3-carbinol (I3C) and other aryl hydrocarbon receptor agonists are known to modulate the immune system and ameliorate various inflammatory and autoimmune diseases in animal models, including colitis induced by dextran sulfate sodium (DSS). MicroRNAs (miRNAs) are also gaining traction as potential therapeutic agents or diagnostic elements. Enterohepatic

aimTo determine whether infection with an EHH species alters the response to I3C and how the immune and miRNA responses of an EHH species compare with responses to DSS and inflammatory bowel disease.

methodsWe infected C57BL/6 mice with

results

conclusionThus, I3C may be useful for inflammatory bowel disease patients regardless of EHH infection. The miRNA changes associated with I3C treatment are likely the result of, rather than the cause of immune response changes.

Indexed as

ColitisMicroRNAsAnimalsColonCytokinesDextran SulfateDisease Models, AnimalHelicobacterHumansIndolesMiceMice, Inbred C57BLCytokinesDextran Sulfateindole-3-carbinolIndolesMicroRNAsColitisCytokineHelicobacter muridarumImmuneMicroRNAT helper 17 cellT regulatory cell

Identifiers

PMID32921956
PMCPMC7459201
OpenAlexW3081645346

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.