Evidence map›Paper›PMID 40196418›Full record

ArticleAnalytical cellular pathology (Amsterdam)2025

Peroxiredoxin 1 Promotes Proinflammatory Cytokine Secretion in Human Dysplastic Oral Keratinocytes and Mouse Tongue Precancerous Tissues.

Min Zhang, Wenjing Li, Jing Li, Wenchao Wang, Lingyu Li, Yunping Lu, Min Wang, Xiaofei Tang

Abstract read
In one paragraph

Article in Analytical cellular pathology (Amsterdam), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Min ZhangBeijing Institute of Dental Research, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0000-0002-9169-1024
Wenjing LiBeijing Institute of Dental Research, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0009-0002-5017-6816
Jing LiBeijing Institute of Dental Research, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0009-0003-3373-326X
Wenchao WangDepartment of Pathology, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0009-0005-8276-928X
Lingyu LiDepartment of Pathology, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0000-0002-1512-2399
Yunping LuDepartment of Prosthodontics, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0000-0003-2577-3272
Min WangBeijing Institute of Dental Research, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0000-0001-6706-3418
Xiaofei TangBeijing Institute of Dental Research, Beijing Stomatological Hospital and School of Stomatology, Capital Medical University, Fengtai District, Beijing 100070, China.ORCID https://orcid.org/0000-0001-6557-7722

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress, a widespread phenomenon involved in many pathological conditions, may be closely related with the progression of oral leukoplakia (OLK). Under chronic inflammation, oxidative stress could stimulate the local formation of a tumor-specific microenvironment in some types of cancer, though not well defined in oral cancer even in OLK. Peroxiredoxin 1 (Prx1), a widely expressed sulfhydryl antioxidant protein, is overexpressed in various tumors and affects tumorigenesis, cell proliferation, apoptosis, invasion, and metastasis. Prx1 also acts as a potent proinflammatory factor. Nuclear factor (NF)-κB is a member of the core dimeric transcription factor family that coordinates the inflammatory response. To investigate the role of Prx1 in oxidative stress-related inflammation in OLK, a coculture model of human dysplastic oral keratinocyte (DOK) and human epidermal fibroblast (HFF) was established and stimulated with H

Indexed as

CytokinesInflammation MediatorsKeratinocytesPeroxiredoxinsPrecancerous ConditionsTongueTongue NeoplasmsAnimalsHumansHydrogen PeroxideInflammationLeukoplakia, OralMiceNF-kappa BOxidative StressReactive Oxygen SpeciesCytokinesHydrogen PeroxideInflammation MediatorsNF-kappa BPeroxiredoxinsPRDX1 protein, humanReactive Oxygen Speciesinflammatory factorsNF-κBoral leukoplakiaPrx1

Identifiers

PMID40196418
PMCPMC11972860

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Registered trials

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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.