Evidence map›Paper›PMID 32581130›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Cyclic GMP-AMP synthase promotes the inflammatory and autophagy responses in Huntington disease.

Manish Sharma, Sumitha Rajendrarao, Neelam Shahani, Uri Nimrod Ramírez-Jarquín, Srinivasa Subramaniam

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 1 pooled it
13.8field-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

102 citing papers in PubMed, 1 synthesis or guideline pooled it, 157 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Targeting the cGAS-STING pathway mitigates Huntington disease pathogenesis in a knock-in mouse model.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Expanding roles of cGAS-STING signaling in neuroinflammation.The Journal of clinical investigation · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. Micronuclei: origins, assays, mechanisms, diseases and treatments.Signal transduction and targeted therapy · 2026
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Article

42 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

5 authors at 1 institution in 1 country.

Manish SharmaDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458.
Sumitha RajendraraoDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458.
Neelam ShahaniDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458.ORCID 0000-0003-1907-4811
Uri Nimrod Ramírez-JarquínDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458.ORCID 0000-0002-0752-1293
Srinivasa SubramaniamDepartment of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458 SSubrama@scripps.edu.
Scripps Research Institute · US

Funding

mTOR Signaling in Striatum: Regulation and FunctionR01NS087019 · NINDS · SCRIPPS FLORIDA · PI SUBRAMANIAM, SRINI · 2015 to 2019
$2.3M
Rhes-SUMO circuitry in Huntington's Disease PathogenesisR01NS094577 · NINDS · SCRIPPS FLORIDA · PI SUBRAMANIAM, SRINI · 2016 to 2019
$1.7M
NINDS NIH HHS R01 NS087019NINDS NIH HHS R01 NS094577
6 · The paper itself

Abstract

Huntington disease (HD) is caused by an expansion mutation of the N-terminal polyglutamine of huntingtin (mHTT). mHTT is ubiquitously present, but it induces noticeable damage to the brain's striatum, thereby affecting motor, psychiatric, and cognitive functions. The striatal damage and progression of HD are associated with the inflammatory response; however, the underlying molecular mechanisms remain unclear. Here, we report that cGMP-AMP synthase (cGAS), a DNA sensor, is a critical regulator of inflammatory and autophagy responses in HD. Ribosome profiling revealed that the

Indexed as

AnimalsAutophagyChemokine CCL5Chemokine CXCL10Corpus StriatumCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseEmbryonic Stem CellsHumansHuntingtin ProteinHuntington DiseaseMiceMice, Inbred C57BLMice, KnockoutMicrotubule-Associated ProteinsNeostriatumNeuronsCCL5 protein, humancGAS protein, humanChemokine CCL5Chemokine CXCL10CXCL10 protein, humanCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHTT protein, humanHuntingtin ProteinMAP1LC3A protein, humanMAP1LC3B protein, humanMicrotubule-Associated ProteinsNucleotidyltransferasesProtein Serine-Threonine KinasesTBK1 protein, humanautophagy fluxcotranslational cleavageHTT-copy numberpro-inflammatory responsestriatal vulnerability

Identifiers

PMID32581130
PMCPMC7354937
OpenAlexW3037980935

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.