Evidence map›Paper›PMID 31988590›Full record

ArticleWorld journal of gastroenterology2020

Su Hyuk Ko, Jong Ik Jeon, Hyun Ae Woo, Jung Mogg Kim

Open access · hybridAbstract 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 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 36% 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, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. The gut microbiota in cancer immunity and immunotherapy.Cellular & molecular immunology · 2025
    Review
  6. Review
  7. Review
  8. Article
  9. International journal of molecular sciences · 2021
    Article
  10. International journal of molecular sciences · 2020
    Article
  11. The Protective Role of Probiotics against Colorectal Cancer.Oxidative medicine and cellular longevity · 2020
    Review
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

4 authors at 1 institution in 1 country.

Su Hyuk KoDepartment of Microbiology and Department of Biomedical Science, Hanyang University College of Medicine and Graduate School of Biomedical Science and Engineering, Seoul 04763, South Korea.
Jong Ik JeonDepartment of Microbiology and Department of Biomedical Science, Hanyang University College of Medicine and Graduate School of Biomedical Science and Engineering, Seoul 04763, South Korea.
Hyun Ae WooGraduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul 03760, South Korea.
Jung Mogg KimDepartment of Microbiology and Department of Biomedical Science, Hanyang University College of Medicine and Graduate School of Biomedical Science and Engineering, Seoul 04763, South Korea. jungmogg@hanyang.ac.kr.
Ewha Womans University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnterotoxigenic

aimTo investigate the role of BFT in HO-1 expression in DCs.

methodsMurine DCs were generated from specific pathogen-free C57BL/6 and Nrf2

resultsHO-1 expression was upregulated in DCs stimulated with BFT. Although BFT activated transcription factors such as NF-κB, AP-1, and Nrf2, activation of NF-κB and AP-1 was not involved in the induction of HO-1 expression in BFT-exposed DCs. Instead, upregulation of HO-1 expression was dependent on Nrf2 activation in DCs. Moreover, HO-1 expression via Nrf2 in DCs was regulated by mitogen-activated protein kinases such as ERK and p38. Furthermore, BFT enhanced the production of reactive oxygen species (ROS) and inhibition of ROS production resulted in a significant decrease of phospho-ERK, phospho-p38, Nrf2, and HO-1 expression.

conclusionThese results suggest that signaling pathways involving ROS-mediated ERK and p38 mitogen-activated protein kinases-Nrf2 activation in DCs are required for HO-1 induction during exposure to ETBF-produced BFT.

Indexed as

AnimalsBacterial ToxinsDendritic CellsEnterotoxinsHeme Oxygenase-1MetalloendopeptidasesMiceMice, Inbred C57BLMitogen-Activated Protein KinasesNF-E2-Related Factor 2Reactive Oxygen SpeciesSignal TransductionUp-RegulationBacterial ToxinsBacteroides fragilis toxinEnterotoxinsHeme Oxygenase-1MetalloendopeptidasesMitogen-Activated Protein KinasesNF-E2-Related Factor 2Reactive Oxygen SpeciesBacteroides fragilis enterotoxinDendritic cellsHeme oxygenase-1Mitogen-activated protein kinasesNrf2Signaling

Identifiers

PMID31988590
PMCPMC6969884
OpenAlexW2998948104

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.