Evidence map›Paper›PMID 36978925›Full record

ArticleAntioxidants (Basel, Switzerland)2023

Loss of Peroxiredoxin IV Protects Mice from Azoxymethane/Dextran Sulfate Sodium-Induced Colorectal Cancer Development.

Pratik Thapa, Hong Jiang, Na Ding, Yanning Hao, Aziza Alshahrani, Eun Y Lee, Junichi Fujii, Qiou Wei

Open access · goldFull text read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2023. 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
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

8 authors at 2 institutions in 2 countries.

Pratik ThapaDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Hong JiangDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Na DingDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Yanning HaoDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Aziza AlshahraniDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Eun Y LeeDepartment of Pathology and Laboratory Medicine, University of Kentucky College of Medicine, Lexington, KY 40506, USA.
Junichi FujiiDepartment of Biomolecular Function, Yamagata University, Yamagata 990-9585, Japan.
Qiou WeiDepartment of Toxicology and Cancer Biology, University of Kentucky College of Medicine, Lexington, KY 40506, USA.ORCID 0000-0001-6752-8692
University of Kentucky · USYamagata University · JP

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI Jennifer F Rogers · 2013 to 2026
$38.3M
TRAINING GRANT IN MOLECULAR MECHANISMS OF TOXICITY.T32ES007266 · NIEHS · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI, MELLON, ISABEL W · 1990 to 2020
$3.7M
Role of Sulfiredoxin in Colorectal Cancer DevelopmentR01CA222596 · NCI · UNIVERSITY OF KENTUCKY · PI WEI, QIOU · 2018 to 2022
$1.7M
NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA222596NCI NIH HHS R01CA222596NIEHS NIH HHS T32 ES007266NIEHS NIH HHS T32ES07266
6 · The paper itself

Abstract

Peroxiredoxin IV (Prx4), a typical two-cysteine-containing member of the peroxidase family, functions as an antioxidant to maintain cellular redox homeostasis through the reduction of reactive oxygen species (ROS) via cycles of oxidation-reduction reactions. Under oxidative stress, all Prxs including Prx4 are inactivated as their catalytic cysteines undergo hyperoxidation, and hyperoxidized two-cysteine Prxs can be exclusively repaired and revitalized through the reduction cycle catalyzed by sulfiredoxin (Srx). Previously, we showed that Prx4 is a preferred substrate of Srx, and knockout of Srx in mice leads to resistance to azoxymethane/dextran sulfate sodium (AOM/DSS)-induced colon carcinogenesis. To further understand the significance of the Srx/Prx4 axis in colorectal cancer development, Prx4

Indexed as

colorectal canceroxidative stressperoxiredoxinredoxsulfiredoxintumorigenesistumor microenvironment

Identifiers

PMID36978925
PMCPMC10045277
OpenAlexW4323844339

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read35
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.