Evidence map›Paper›PMID 34406707›Full record

ArticleMolecular nutrition & food research2021

Role of the Aryl Hydrocarbon Receptor (AhR) in Mediating the Effects of Coffee in the Colon.

Robert S Chapkin, Laurie A Davidson, Hyejin Park, Un-Ho Jin, Yang-Yi Fan, Yating Cheng, Martha E Hensel, Kerstin K Landrock, Clinton Allred, Rani Menon and 3 more

Open access · greenAbstract read
In one paragraph

Article in Molecular nutrition & food research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 18 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

13 authors at 1 institution in 1 country.

Robert S ChapkinDepartments of Nutrition and Biochemistry & Biophysics Texas A&M University, College Station, TX, 77843, USA.
Laurie A DavidsonDepartments of Nutrition and Biochemistry & Biophysics Texas A&M University, College Station, TX, 77843, USA.
Hyejin ParkDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, 77843, USA.
Un-Ho JinDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, 77843, USA.
Yang-Yi FanDepartments of Nutrition and Biochemistry & Biophysics Texas A&M University, College Station, TX, 77843, USA.
Yating ChengDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, 77843, USA.
Martha E HenselDepartment of Veterinary Pathobiology, Texas A&M University, College Station, TX, 77843, USA.
Kerstin K LandrockDepartments of Nutrition and Biochemistry & Biophysics Texas A&M University, College Station, TX, 77843, USA.
Clinton AllredDepartments of Nutrition and Biochemistry & Biophysics Texas A&M University, College Station, TX, 77843, USA.
Rani MenonDepartment of Chemical Engineering, Texas A&M University, College Station, TX, 77843, USA.
Cory KlemashevichDepartment of Chemical Engineering, Texas A&M University, College Station, TX, 77843, USA.
Arul JayaramanDepartment of Chemical Engineering, Texas A&M University, College Station, TX, 77843, USA.
Stephen SafeDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, 77843, USA.ORCID 0000-0002-2115-3060
Texas A&M University · US

Funding

Texas A&M Center for Environmental Health Research (TiCER)P30ES029067 · NIEHS · TEXAS A&M UNIVERSITY · PI Galen Newman · 2019 to 2026
$13.0M
Plasma membrane therapy: Disruption of Wnt associated receptor spatiotemporal organization by membrane targeted dietary bioactives (MTDB)R35CA197707 · NCI · TEXAS A&M AGRILIFE RESEARCH · PI CHAPKIN, ROBERT STEPHEN · 2016 to 2022
$6.3M
Diet induced modifications of microbiota metabolites in colon tumorigenesisR01CA202697 · NCI · TEXAS A&M AGRILIFE RESEARCH · PI ALLRED, CLINTON D, CHAPKIN, ROBERT STEPHEN · 2016 to 2020
$2.0M
Microbial flavonoid metabolites as modulators of AD markers in a 3D human neural tissue modelR01AT010282 · NCCIH · TEXAS A&M AGRILIFE RESEARCH · PI CHAPKIN, ROBERT STEPHEN, JAYARAMAN, ARUL · 2018 to 2021
$1.9M
NCCIH NIH HHS R01 AT010282NCI NIH HHS R01 CA202697NCI NIH HHS R35 CA197707NIEHS NIH HHS P30 ES029067
6 · The paper itself

Abstract

scopeThis study investigates the mechanism of action and functional effects of coffee extracts in colonic cells, on intestinal stem cell growth, and inhibition of dextran sodium sulfate (DSS)-induced intestinal barrier damage in mice. METHODS AND

resultsAqueous coffee extracts induced Ah receptor (AhR) -responsive CYP1A1, CYP1B1, and UGT1A1 gene expression in colon-derived Caco2 and YAMC cells. Tissue-specific AhR knockout (AhR

conclusionsIn colon-derived cells and in the mouse intestine, coffee induced several AhR-dependent responses including gene expression, inhibition of intestinal stem cell-enriched organoid growth, and inhibition of DSS-induced intestinal barrier damage. We conclude that the anti-inflammatory effects of coffee in the intestine are due, in part, to activation of AhR signaling.

Indexed as

CoffeeAnimalsCaco-2 CellsColonCytochrome P-450 CYP1A1Cytochrome P-450 CYP1B1Dextran SulfateFemaleHumansMaleMicePlant ExtractsReceptors, Aryl HydrocarbonCoffeeCYP1B1 protein, humanCytochrome P-450 CYP1A1Cytochrome P-450 CYP1B1Dextran SulfatePlant ExtractsReceptors, Aryl HydrocarbonAhRanti-inflammatoryCoffeecolonic stem cellsCYP1A1

Identifiers

PMID34406707
PMCPMC8530922
OpenAlexW3194159070

What OpenQuestion holds

Textmetadata
LicenceTDM
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.