Evidence map›Paper›PMID 25651846›Full record

ReviewActa biochimica et biophysica Sinica2015

Regulation of cellular innate antiviral signaling by ubiquitin modification.

Dandan Lin, Bo Zhong

Abstract readReview
In one paragraph

Review in Acta biochimica et biophysica Sinica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Dandan LinDepartment of Oncology, Renmin Hospital, Wuhan University, Wuhan 430060, China.
Bo ZhongState Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China zhongbo@whu.edu.cn.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Host pattern-recognition receptors (PRRs) recognize pathogen-associated molecular patterns generated by invading viruses and initiate a series of signaling cascades that lead to the activation of interferon-regulatory factor 3 (IRF3) and nuclear factor-κB (NF-κB) and subsequent induction of type I interferons (IFNs). Posttranslational modification of proteins by ubiquitin plays an essential role in mediating or regulating the virus-triggered PRRs-mediated signaling. Deubiquitination is the reversible process of ubiquitination and its role in regulating PRRs-mediated signaling has recently been explored. In this review, we first summarize the ubiquitination events in PRRs-mediated signaling that is triggered by viral nucleic acid and then focus on host and viral deubiquitinating enzymes-mediated regulation of virus-triggered signaling that modulates the activation of IRF3 and NF-κB and subsequent induction of type I IFNs.

Indexed as

Host-Pathogen InteractionsHumansImmunity, CellularImmunity, InnateInterferon Regulatory Factor-3NF-kappa BPathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionSignal TransductionToll-Like ReceptorsUbiquitinationUbiquitin-Specific ProteasesVirusesInterferon Regulatory Factor-3IRF3 protein, humanNF-kappa BPathogen-Associated Molecular Pattern MoleculesReceptors, Pattern RecognitionToll-Like ReceptorsUbiquitin-Specific Proteasescellular innate antiviral signalingpattern-recognition receptorubiquitin modification

Identifiers

PMID25651846
PMCPMC7109689
OpenAlexW2134949572

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.