Evidence map›Paper›PMID 39112770›Full record

ReviewActa pharmacologica Sinica2025

Cyclic GMP-AMP synthase recognizes the physical features of DNA.

Ling Dong, Yue-Ru Hou, Na Xu, Xiao-Qian Gao, Zhen Sun, Qing-Kai Yang, Li-Na Wang

Registry-linked trialAbstract readReview
In one paragraph

Review in Acta pharmacologica Sinica, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07573735 (An Observational Study on the Correlation Between Circulating Cell-free DNA and Skin Macrophage STING Pathway Activation in Patients With Atopic Dermatitis), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT07573735 recruitingnot on this mapstarted 2026, after this paper: background citation

An Observational Study on the Correlation Between Circulating Cell-free DNA and Skin Macrophage STING Pathway Activation in Patients With Atopic Dermatitis

Typeobservational_patient_registrySponsorZhongda HospitalRan2026 to 2026Enrolled80ConditionsAtopic Dermatitis (Eczema)Armsblood sampling
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Review
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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

7 authors.

Ling DongInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China.
Yue-Ru HouInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China.
Na XuInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China.
Xiao-Qian GaoInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China.
Zhen SunInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China.
Qing-Kai YangInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China. Yangqingkai@dmu.edu.cn.
Li-Na WangInstitute of Cancer Stem Cell, DaLian Medical University, Dalian, 116044, China. li-nawang@dmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cyclic GMP-AMP synthase (cGAS) is a major cytosolic DNA sensor that plays a significant role in innate immunity. Upon binding to double stranded DNA (dsDNA), cGAS utilizes GTP and ATP to synthesize the second messenger cyclic GMP-AMP (cGAMP). The cGAMP then binds to the adapter protein stimulator of interferon genes (STING) in the endoplasmic reticulum, resulting in the activation of the transcription factor interferon regulatory factor 3 (IRF3) and subsequent induction of type I interferon. An important question is how cGAS distinguishes between self and non-self DNA. While cGAS binds to the phosphate backbone of DNA without discrimination, its activation is influenced by physical features such as DNA length, inter-DNA distance, and mechanical flexibility. This suggests that the recognition of DNA by cGAS may depend on these physical features. In this article we summarize the recent progress in research on cGAS-STING pathway involved in antiviral defense, cellular senescence and anti-tumor response, and focus on DNA recognition mechanisms based on the physical features.

Indexed as

DNAMembrane ProteinsNucleotidyltransferasesAnimalsCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHumansImmunity, InnateNucleotides, CyclicSTING ProteincGAS protein, humancyclic guanosine monophosphate-adenosine monophosphateCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNAMembrane ProteinsNucleotides, CyclicNucleotidyltransferasesSTING1 protein, humanSTING Proteincyclic GMP-AMP synthasecytosolic DNA sensorDNA physical featuresinnate immune responseSTING

Identifiers

PMID39112770
PMCPMC11747433

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Registered trials

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.