Evidence map›Paper›PMID 36685512›Full record

ArticleFrontiers in immunology2022

Genetic analysis of potential biomarkers and therapeutic targets in ferroptosis from psoriasis.

Man-Ning Wu, Dong-Mei Zhou, Chun-Yan Jiang, Wei-Wen Chen, Jia-Chi Chen, Yue-Min Zou, Tao Han, Li-Jia-Ming Zhou

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

21 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Ferroptosis: Disease Associations and Therapeutic Target Exploration.Journal of molecular neuroscience : MN · 2025
    Review
  11. Article
  12. Article
  13. Dialogue between programmed cell death and psoriasis.Postepy dermatologii i alergologii · 2025
    Review
  14. Article
  15. Article
  16. Article
  17. The diagnostic value and associated molecular mechanism study for fibroblast-related mitochondrial genes on keloid.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2024
    Article
  18. Article
  19. Review
  20. 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 1 country.

Man-Ning WuDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Dong-Mei ZhouDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Chun-Yan JiangDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Wei-Wen ChenDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Jia-Chi ChenDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Yue-Min ZouDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Tao HanDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Li-Jia-Ming ZhouDepartment of Dermatology, Beijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Capital Medical University · CNBeijing Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Ferroptosis is associated with multiple pathophysiological processes. Inhibition of ferroptosis has received much concern for some diseases. Nonetheless, there is no study comprehensively illustrating functions of ferroptosis-related genes (FRGs) in psoriasis. Methods: In this study, FRGs together with psoriasis-associated data were obtained in Ferroptosis Database (FerrDb) and gene expression omnibus (GEO) database separately. This work identified altogether 199 psoriasis-associated DE-FRGs, and they were tightly associated with immunity and autophagy modulation. Thereafter, the present study utilized SVM-RFE and LASSO algorithms to identify NR5A2, CISD1, GCLC, PRKAA2, TRIB2, ABCC5, ACSF2, TIMM9, DCAF7, PEBP1, and MDM2 from those 199 DE-FRGs to be marker genes. As revealed by later functional annotation, the marker genes possibly had important effects on psoriasis through being involved in diverse psoriasis pathogenesis-related pathways such as cell cycle, toll-like receptor (TLR), chemokine, and nod-like receptor (NLR) pathways. Moreover, altogether 37 drugs that targeted 11 marker genes were acquired. Besides, based on CIBERSORT analysis, alterations of immune microenvironment in psoriasis cases were possibly associated with PRKAA2, PEBP1, CISD1, and ACSF2. Discussion: Taken together, this work established the diagnostic potency and shed more lights on psoriasis-related mechanism. More investigations are warranted to validate its value in diagnosing psoriasis before it is applied in clinic.

Indexed as

FerroptosisPsoriasisAlgorithmsAutophagyBiomarkersCalcium-Calmodulin-Dependent Protein KinasesHumansBiomarkersCalcium-Calmodulin-Dependent Protein KinasesTRIB2 protein, humanbioinformaticsdiagnosticferroptosisimmune microenvironmentpsoriasis

Identifiers

PMID36685512
PMCPMC9846571
OpenAlexW4313584662

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.