Evidence map›Paper›PMID 39815286›Full record

ReviewJournal of translational medicine2025

Exploring TNFR1: from discovery to targeted therapy development.

Yingying Li, Ruiwei Ye, Haorui Dai, Jiayi Lin, Yue Cheng, Yonghong Zhou, Yiming Lu

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. Article
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  7. Materials today. Bio · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. The Role of TNF-α in Ischemic Stroke.International journal of molecular sciences · 2026
    Review
  18. Article
  19. Review
  20. 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

7 authors.

Yingying Li *School of Medicine, Shanghai Baoshan Luodian Hospital, Shanghai University, Shanghai, 201908, China.
Ruiwei Ye *Department of Pharmacy, School of Medicine, Shanghai University, Shanghai, 200444, China.
Haorui Dai *Department of Pharmacy, School of Medicine, Shanghai University, Shanghai, 200444, China.
Jiayi LinDepartment of Pharmacy, School of Medicine, Shanghai University, Shanghai, 200444, China.
Yue ChengDepartment of Pharmacy, School of Medicine, Shanghai University, Shanghai, 200444, China.
Yonghong ZhouDepartment of Pharmacy, School of Medicine, Shanghai University, Shanghai, 200444, China. zhouyonghong1989@163.com.
Yiming LuSchool of Medicine, Shanghai Baoshan Luodian Hospital, Shanghai University, Shanghai, 201908, China. bluesluyi@sina.com.ORCID 0000-0003-3497-1860

Funding

National Natural Science Foundation of China 42076094National Natural Science Foundation of China 81773627National Natural Science Foundation of China 82473835Shanghai Science and Technology Innovation Action Plan 21S11902400
6 · The paper itself

Abstract

This review seeks to elucidate the therapeutic potential of tumor necrosis factor receptor 1 (TNFR1) and enhance our comprehension of its role in disease mechanisms. As a critical cell-surface receptor, TNFR1 regulates key signaling pathways, such as nuclear factor kappa-B (NF-κB) and mitogen-activated protein kinase (MAPK), which are associated with pro-inflammatory responses and cell death. The intricate regulatory mechanisms of TNFR1 signaling and its involvement in various diseases, including inflammatory disorders, infectious diseases, cancer, and metabolic syndromes, have attracted increasing scholarly attention. Given the potential risks associated with targeting tumor necrosis factor-alpha (TNF-α), selective inhibition of the TNFR1 signaling pathway has been proposed as a promising strategy to reduce side effects and enhance therapeutic efficacy. This review emphasizes the emerging field of targeted therapies aimed at selectively modulating TNFR1 activity, identifying promising therapeutic strategies that exploit TNFR1 as a drug target through an evaluation of current clinical trials and preclinical studies. In conclusion, this study contributes novel insights into the biological functions of TNFR1 and presents potential therapeutic strategies for clinical application, thereby having substantial scientific and clinical significance.

Indexed as

Drug DiscoveryMolecular Targeted TherapyReceptors, Tumor Necrosis Factor, Type IAnimalsHumansSignal TransductionReceptors, Tumor Necrosis Factor, Type IApoptosisInflammationTherapyTNFTNFR1

Identifiers

PMID39815286
PMCPMC11734553

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.