Evidence map›Paper›PMID 38002251›Full record

ReviewBiomolecules2023

APE1/Ref-1 as a Therapeutic Target for Inflammatory Bowel Disease.

Lauren Sahakian, Ainsley M Robinson, Linda Sahakian, Rhian Stavely, Mark R Kelley, Kulmira Nurgali

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Yerba Mate (Nutrients · 2024
    Article
  10. Review
  11. Article
  12. Article
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

6 authors at 4 institutions in 2 countries.

Lauren SahakianInstitute for Health & Sport, Victoria University, Melbourne, VIC 3021, Australia.
Ainsley M RobinsonInstitute for Health & Sport, Victoria University, Melbourne, VIC 3021, Australia.
Linda SahakianDepartment of Medicine Western Health, The University of Melbourne, Melbourne, VIC 3010, Australia.
Rhian StavelyDepartment of Medicine Western Health, The University of Melbourne, Melbourne, VIC 3010, Australia.ORCID 0000-0002-5099-3704
Mark R KelleyDepartment of Pediatrics, Herman B Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.ORCID 0000-0001-9472-1826
Kulmira NurgaliInstitute for Health & Sport, Victoria University, Melbourne, VIC 3021, Australia.ORCID 0000-0002-2597-6929
The University of Melbourne · AUHarvard University · USIndiana University School of MedicineVictoria University · AU

Funding

Metabolic flux analysis and PDX models to understand therapeutic vulnerabilities following inhibition of Ref-1 redox signaling in pancreatic cancerR01CA282478 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI Melissa L. Fishel, Mark R. Kelley · 2023 to 2026
$2.1M
Crohn's and Colitis Foundation 903433NCI NIH HHS R01 CA282478
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is characterized by chronic relapsing inflammation of the gastrointestinal tract. The prevalence of IBD is increasing with approximately 4.9 million cases reported worldwide. Current therapies are limited due to the severity of side effects and long-term toxicity, therefore, the development of novel IBD treatments is necessitated. Recent findings support apurinic/apyrimidinic endonuclease 1/reduction-oxidation factor 1 (APE1/Ref-1) as a target in many pathological conditions, including inflammatory diseases, where APE1/Ref-1 regulation of crucial transcription factors impacts significant pathways. Thus, a potential target for a novel IBD therapy is the redox activity of the multifunctional protein APE1/Ref-1. This review elaborates on the status of conventional IBD treatments, the role of an APE1/Ref-1 in intestinal inflammation, and the potential of a small molecule inhibitor of APE1/Ref-1 redox activity to modulate inflammation, oxidative stress response, and enteric neuronal damage in IBD.

Indexed as

Inflammatory Bowel DiseasesOxidative StressDNA-(Apurinic or Apyrimidinic Site) LyaseHumansInflammationOxidation-ReductionDNA-(Apurinic or Apyrimidinic Site) Lyaseapurinic/apyrimidinic endonuclease 1/reduction-oxidation factor 1 (APE1/Ref-1)inflammationinflammatory bowel disease (IBD)oxidative stressredox signaling

Identifiers

PMID38002251
PMCPMC10669584
OpenAlexW4387907770

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.