Evidence map›Paper›PMID 35732833›Full record

ReviewNature reviews. Nephrology2022

Role of the cGAS-STING pathway in systemic and organ-specific diseases.

Sladjana Skopelja-Gardner, Jie An, Keith B Elkon

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Nephrology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
21.3field-weighted citation impact, top 1% of its field
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

187 citing papers in PubMed, 272 citations in OpenAlex.

  1. Review
  2. T-Cell Remodeling in Renal Fibrosis: From Acute Injury to Chronic Kidney Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  3. Review
  4. Review
  5. Self-assembled supramolecular nanoparticles ofActa pharmaceutica Sinica. B · 2026
    Article
  6. cGAS-STING as a Neuroimmune Traffic Molecule: Unraveling Pathogenic Mechanisms and Therapeutic Potential in Neurological Disorders.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Lactylation: a novel post-translational modification for cGAS-STING pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Autoinflammatory syndromes of STING and TREX1 dysfunction.The Journal of clinical investigation · 2026
    Review
  20. Article

127 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Sladjana Skopelja-GardnerDepartment of Medicine, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA.
Jie AnDepartment of Medicine, University of Washington, Seattle, WA, USA.
Keith B ElkonDepartment of Medicine, University of Washington, Seattle, WA, USA. kelkon@medicine.washington.edu.ORCID http://orcid.org/0000-0002-7340-6146
University of Washington · USDartmouth–Hitchcock Medical Center · US

Funding

cGAMP as an immunotransmitter of the interferon response to UV lightR21AR077842 · NIAMS · UNIVERSITY OF WASHINGTON · PI ELKON, KEITH B. · 2021 to 2021
$427k
VISTA regulates type I interferon response to ultraviolet lightR21AR079661 · NIAMS · DARTMOUTH-HITCHCOCK CLINIC · PI SKOPELJA-GARDNER, SLADJANA · 2021 to 2021
$384k
NIAMS NIH HHS R21 AR077842NIAMS NIH HHS R21 AR079661
6 · The paper itself

Abstract

Cells are equipped with numerous sensors that recognize nucleic acids, which probably evolved for defence against viruses. Once triggered, these sensors stimulate the production of type I interferons and other cytokines that activate immune cells and promote an antiviral state. The evolutionary conserved enzyme cyclic GMP-AMP synthase (cGAS) is one of the most recently identified DNA sensors. Upon ligand engagement, cGAS dimerizes and synthesizes the dinucleotide second messenger 2',3'-cyclic GMP-AMP (cGAMP), which binds to the endoplasmic reticulum protein stimulator of interferon genes (STING) with high affinity, thereby unleashing an inflammatory response. cGAS-binding DNA is not restricted by sequence and must only be >45 nucleotides in length; therefore, cGAS can also be stimulated by self genomic or mitochondrial DNA. This broad specificity probably explains why the cGAS-STING pathway has been implicated in a number of autoinflammatory, autoimmune and neurodegenerative diseases; this pathway might also be activated during acute and chronic kidney injury. Therapeutic manipulation of the cGAS-STING pathway, using synthetic cyclic dinucleotides or inhibitors of cGAMP metabolism, promises to enhance immune responses in cancer or viral infections. By contrast, inhibitors of cGAS or STING might be useful in diseases in which this pro-inflammatory pathway is chronically activated.

Indexed as

Interferon Type IMembrane ProteinsCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNAHumansNucleotidyltransferasesSignal TransductionSTING ProteincGAS protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseDNAInterferon Type IMembrane ProteinsNucleotidyltransferasesSTING1 protein, humanSTING Protein

Identifiers

PMID35732833
PMCPMC9214686
OpenAlexW4283360769

What OpenQuestion holds

Textmetadata
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.