Evidence map›Paper›PMID 39041676›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2024

Endogenous glucocorticoids are required for normal macrophage activation and gastric

Stuti Khadka, Sebastian A Dziadowicz, Xiaojiang Xu, Lei Wang, Gangqing Hu, Javier A Carrero, Richard J DiPaolo, Jonathan T Busada

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Stuti KhadkaDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Sebastian A DziadowiczDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Xiaojiang XuDepartment of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana, United States.
Lei WangDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Gangqing HuDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.
Javier A CarreroDepartment of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States.
Richard J DiPaoloDepartment of Molecular Microbiology and Immunology, Saint Louis University School of Medicine, Saint Louis, Missouri, United States.
Jonathan T BusadaDepartment of Microbiology, Immunology, and Cell Biology, West Virginia University School of Medicine, Morgantown, West Virginia, United States.ORCID 0000-0001-5886-9858

Funding

West Virginia IDEA-CTRU54GM104942 · NIGMS · WEST VIRGINIA UNIVERSITY · PI JUDITH FEINBERG · 2012 to 2026
$81.0M
WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
WVU Flow Cytometry and Single Cell Core Facility (FCSCCF)P20GM121322 · NIGMS · WEST VIRGINIA UNIVERSITY · PI Karen H Martin · 2018 to 2026
$22.4M
COBRE Transitional Center in NeuroscienceP30GM103503 · NIGMS · WEST VIRGINIA UNIVERSITY · PI SPIROU, GEORGE A · 2012 to 2014
$3.2M
The Role of Inflammation in Regulating Gastric MetaplasiaR01DK134531 · NIDDK · SAINT LOUIS UNIVERSITY · PI Richard J DiPaolo · 2023 to 2026
$2.1M
Cytek 3-laser AuroraS10OD028605 · OD · WEST VIRGINIA UNIVERSITY · PI BRUNDAGE, KATHLEEN M · 2021 to 2021
$259k
HHS | National Institutes of Health (NIH) P20GM121322NIDDK NIH HHS R01 DK134531NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P20 GM121322NIGMS NIH HHS P30 GM103503NIGMS NIH HHS U54 GM104942NIH HHS S10 OD028605
6 · The paper itself

Abstract

Glucocorticoids are steroid hormones well known for their potent anti-inflammatory effects. However, their immunomodulatory properties are multifaceted. Increasing evidence suggests that glucocorticoid signaling promotes effective immunity and that disruption of glucocorticoid signaling impairs immune function. In this study, we conditionally deleted the glucocorticoid receptor (GR) in the myeloid lineage using the

Indexed as

GlucocorticoidsHelicobacter InfectionsHelicobacter pyloriMacrophage ActivationMacrophagesMice, KnockoutReceptors, GlucocorticoidAnimalsGastric MucosaMiceSignal TransductionGlucocorticoidsReceptors, GlucocorticoidglucocorticoidHelicobacter pylorimacrophagepyloric metaplasia

Identifiers

PMID39041676
PMCPMC11482275

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.