Evidence map›Paper›PMID 41811896›Full record

ReviewJournal of immunology research2026

A Comprehensive Review of AIM2 in Cancer: Functional Roles, Molecular Pathways, and Clinical Relevance.

Nuo Wang, Shaoxian Wu, Zhang Fang, Lujun Chen, Xiao Zheng

Abstract readReview
In one paragraph

Review in Journal of immunology research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

5 authors.

Nuo WangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China, suda.edu.cn.
Shaoxian WuDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China, suda.edu.cn.
Zhang FangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China, suda.edu.cn.
Lujun ChenDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China, suda.edu.cn.
Xiao ZhengDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University, Changzhou, Jiangsu, China, suda.edu.cn.ORCID https://orcid.org/0000-0002-6163-7414

Funding

Jiangsu Funding Program for Excellent Postdoctoral Talent 2023ZB512Key R&D Project of Jiangsu Province BE2022721National Natural Science Foundation of China 82172689National Natural Science Foundation of China 82303164Science and Technology Support Plan (Social Development) Project of Changzhou CE20235058
6 · The paper itself

Abstract

Inflammation has been recognized as a component of cancer progression, and inflammasome receptor components also regulate various biological processes, including cell proliferation, gene transcription, and tumorigenesis. Accumulating evidence indicates that the AIM2 inflammasome influences tumor progression via multiple concurrent mechanisms, one of which involves the negative regulation of STING-dependent type I interferon signaling. Consequently, AIM2 may be a potential molecular target for cancer immunotherapy, and further studies are expected to reveal its application prospects in cancer therapy. Extensive research has been published on AIM2 in colorectal cancer, although it is known to also function in many other cancers. This review summarizes the diverse modes through which AIM2 in different cancers and discusses the possible future clinical application of AIM2. This review aims to provide more evidence for better methods of cancer treatment.

Indexed as

DNA-Binding ProteinsNeoplasmsAnimalsHumansImmunotherapyInflammasomesInterferon Type IMolecular Targeted TherapySignal TransductionAIM2 protein, humanDNA-Binding ProteinsInflammasomesInterferon Type Iabsent in melanoma 2biological mechanismscancerimmunotherapypyroptosis

Identifiers

PMID41811896
PMCPMC13140378

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.