Evidence map›Paper›PMID 40007541›Full record

ReviewFrontiers in immunology2025

RIPK1 in necroptosis and recent progress in related pharmaceutics.

Kunhou Yao, Zhihao Shi, Fengya Zhao, Cong Tan, Yixin Zhang, Hao Fan, Yingzhe Wang, Xingwang Li, Jun Kong, Qun Wang and 1 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  7. Article
  8. Necroptosis in Down Syndrome.Cell death & disease · 2026
    Article
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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

11 authors.

Kunhou Yao *Department of General Surgery, Huaihe Hospital of Henan University, Kaifeng, China.
Zhihao Shi *School of Basic Medicine, Henan University, Kaifeng, China.
Fengya Zhao *School of Basic Medicine, Henan University, Kaifeng, China.
Cong TanSchool of Basic Medicine, Henan University, Kaifeng, China.
Yixin ZhangSchool of Basic Medicine, Henan University, Kaifeng, China.
Hao FanSchool of Basic Medicine, Henan University, Kaifeng, China.
Yingzhe WangSchool of Basic Medicine, Henan University, Kaifeng, China.
Xingwang LiDepartment of General Surgery, Huaihe Hospital of Henan University, Kaifeng, China.
Jun KongSchool of Basic Medicine, Henan University, Kaifeng, China.
Qun WangSchool of Basic Medicine, Henan University, Kaifeng, China.
Dingxi LiDepartment of Gynaecology, The Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necroptosis is a programmed form of cell death. Receptor-interacting serine/threonine protein kinase l (RIPK1) is a crucial protein kinase that regulates the necroptosis pathway. Increased expression of death receptor family ligands such as tumor necrosis factor (TNF) increases the susceptibility of cells to apoptosis and necroptosis. RIPK1, RIPK3, and mixed-lineage kinase-like domain (MLKL) proteins mediate necrosis. RIPK1-mediated necroptosis further promotes cell death and inflammation in the pathogenesis of liver injury, skin diseases, and neurodegenerative diseases. The N-terminal kinase domain of RIPK1 is significant in the induction of cell death and can be used as a vital drug target for inhibitors. In this paper, we outline the pathways of necroptosis and the role RIPK1 plays in them and suggest that targeting RIPK1 in therapy may help to inhibit multiple cell death pathways.

Indexed as

NecroptosisReceptor-Interacting Protein Serine-Threonine KinasesAnimalsApoptosisHumansNecrosisSignal TransductionReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, humaninflammationkinase domainnecroptosispharmaceuticsprogrammed cell deathRIPK1

Identifiers

PMID40007541
PMCPMC11850271

What OpenQuestion holds

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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.