Evidence map›Paper›PMID 41888126›Full record

ReviewCell death discovery2026

The role of NINJ1 in diseases.

Shijun Bao, Fengxu Chen, Ziyi Guo, Wen Ding, Fu Gao, Jiaming Guo

Abstract readReview
In one paragraph

Review in Cell death discovery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

6 authors.

Shijun Bao *Department of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China.
Fengxu Chen *Department of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China.
Ziyi Guo *Department of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China.
Wen DingDepartment of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China.
Fu GaoDepartment of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China. gaofusmmu@163.com.
Jiaming GuoDepartment of Radiation Medicine, College of Naval Medicine, Naval Medical University, Shanghai, China. smmuguojiaming@126.com.ORCID http://orcid.org/0000-0001-9898-237X

Funding

Natural Science Foundation of Shanghai (Natural Science Foundation of Shanghai Municipality) 24ZR1480000
6 · The paper itself

Abstract

Nerve injury-induced protein 1 (NINJ1) is a multifunctional membrane protein historically studied for its roles in nerve regeneration and cell adhesion. A groundbreaking study fundamentally revised our understanding by demonstrating that NINJ1 acts as the active executor of plasma membrane rupture in lytic cell death pathways such as pyroptosis and ferroptosis, establishing this final step as a biologically regulated process. Recent structural insights now reveal that NINJ1 adopts distinct molecular forms-including the full-length monomer, a soluble fragment, and a membrane-rupturing oligomer-which dictate its functional roles in adhesion, chemotaxis, and cell lysis. This revised understanding calls for a systematic integration of previous observations, particularly given NINJ1's context-dependent and often contradictory roles in inflammation, cancer, and tissue injury. Here, we review the structural basis of NINJ1 function, its pathological implications, and propose a unified structure-function model to reconcile its diverse phenotypes and bridge its traditional roles with its newly identified function in membrane rupture.

Identifiers

PMID41888126
PMCPMC13144334

What OpenQuestion holds

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LicenceCC BY
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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.