Evidence map›Paper›PMID 38118451›Full record

ReviewMolecular cell2024

The competitive landscape of the dsRNA world.

Kyle A Cottrell, Ryan J Andrews, Brenda L Bass

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
10.8field-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

68 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Transcription start site heterogeneity controls MDA5 sensing of unspliced HIV-1 RNAs.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  12. Article
  13. Review
  14. Mitochondrial double-stranded RNA fuels pancreatic cancer growth via RIG-I/TLR3 inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. RNase L Regulates Antiviral Responsiveness through Cleavage of XBP1 mRNA.bioRxiv : the preprint server for biology · 2026
    Article
  20. Article

8 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.

Kyle A CottrellDepartment of Biochemistry, Purdue University, West Lafayette, IN, USA. Electronic address: kacottre@purdue.edu.
Ryan J AndrewsDepartment of Biochemistry, University of Utah, Salt Lake City, UT, USA.
Brenda L BassDepartment of Biochemistry, University of Utah, Salt Lake City, UT, USA. Electronic address: bbass@biochem.utah.edu.
University of Utah · USPurdue University West Lafayette · US

Funding

Unlocking evolutionarily latent immune functions for treating diseaseR01CA260414 · NCI · UNIVERSITY OF UTAH · PI BASS, BRENDA L., ELDE, NELS C. · 2020 to 2024
$5.8M
Elucidating roles and mechanisms of double-stranded RNA-mediated pathwaysR35GM141262 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Brenda L. Bass · 2021 to 2026
$3.7M
Identifying determinants of ADAR-dependency in triple-negative breast cancerR00MD016946 · NIMHD · PURDUE UNIVERSITY · PI COTTRELL, KYLE · 2023 to 2025
$722k
NCI NIH HHS R01 CA260414NIGMS NIH HHS R35 GM141262NIMHD NIH HHS R00 MD016946
6 · The paper itself

Abstract

The ability to sense and respond to infection is essential for life. Viral infection produces double-stranded RNAs (dsRNAs) that are sensed by proteins that recognize the structure of dsRNA. This structure-based recognition of viral dsRNA allows dsRNA sensors to recognize infection by many viruses, but it comes at a cost-the dsRNA sensors cannot always distinguish between "self" and "nonself" dsRNAs. "Self" RNAs often contain dsRNA regions, and not surprisingly, mechanisms have evolved to prevent aberrant activation of dsRNA sensors by "self" RNA. Here, we review current knowledge about the life of endogenous dsRNAs in mammals-the biosynthesis and processing of dsRNAs, the proteins they encounter, and their ultimate degradation. We highlight mechanisms that evolved to prevent aberrant dsRNA sensor activation and the importance of competition in the regulation of dsRNA sensors and other dsRNA-binding proteins.

Indexed as

RNA, Double-StrandedVirus DiseasesAnimalsDEAD-box RNA HelicasesImmunity, InnateMammalsDEAD-box RNA HelicasesRNA, Double-StrandedADARantiviralDHX9dsRNA-binding proteinsinnate immunityinterferonMDA5PKRRIG-I

Identifiers

PMID38118451
PMCPMC10843539
OpenAlexW4389955887

What OpenQuestion holds

Textmetadata
LicenceTDM
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.