Evidence map›Paper›PMID 27282740›Full record

ArticleScientific reports2016

Cell-death-inducing DFFA-like Effector B Contributes to the Assembly of Hepatitis C Virus (HCV) Particles and Interacts with HCV NS5A.

Hua Cai, Wenxia Yao, Leike Li, Xinlei Li, Longbo Hu, Runming Mai, Tao Peng

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Whole Lotta Lipids-from HCV RNA Replication to the Mature Viral Particle.International journal of molecular sciences · 2020
    Review
  5. Review
  6. Article
  7. Review
  8. Kinesin-dependent mechanism for controlling triglyceride secretion from the liver.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  9. Article
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 at 4 institutions in 2 countries.

Hua CaiState Key Laboratory of Respiratory Disease, Guangzhou Hoffmann Institute, College of Basic Sciences, Guangzhou Medical University, Guangzhou, China.
Wenxia YaoState Key Laboratory of Respiratory Disease, Guangzhou Hoffmann Institute, College of Basic Sciences, Guangzhou Medical University, Guangzhou, China.
Leike LiGuangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Xinlei LiState Key Laboratory of Respiratory Disease, Guangzhou Hoffmann Institute, College of Basic Sciences, Guangzhou Medical University, Guangzhou, China.
Longbo HuGuangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Runming MaiState Key Laboratory of Respiratory Disease, Guangzhou Hoffmann Institute, College of Basic Sciences, Guangzhou Medical University, Guangzhou, China.
Tao PengState Key Laboratory of Respiratory Disease, Guangzhou Hoffmann Institute, College of Basic Sciences, Guangzhou Medical University, Guangzhou, China.
Chinese Academy of Sciences · CNGuangzhou Institutes of Biomedicine and Health · CNGuangzhou Medical University · CNState Key Laboratory of Respiratory Disease · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis C virus (HCV) uses components of the very-low-density lipoprotein (VLDL) pathway for assembly/release. We previously reported that hepatocyte nuclear factor 4α (HNF4α) participates in HCV assembly/release through downstream factors those participate in VLDL assembly/secretion. Cell-death-inducing DFFA-like effector B (CIDEB) is an important regulator of the VLDL pathway. CIDEB is required for entry of HCV particles from cell culture (HCVcc), but the effects of CIDEB on the post-entry steps of the HCV lifecycle are unclear. In the present study, we determined that CIDEB is required for HCV assembly in addition to HCVcc entry. Furthermore, CIDEB interacts with the HCV NS5A protein, and the N terminus of CIDEB and the domain I of NS5A are involved in this interaction. Moreover, CIDEB silencing impairs the association of apolipoprotein E (ApoE) with HCV particles. Interestingly, CIDEB is also required for the post-entry stages of the dengue virus (DENV) life cycle. Collectively, these results indicate that CIDEB is a new host factor that is involved in HCV assembly, presumably by interacting with viral protein, providing new insight into the exploitation of the VLDL regulator CIDEB by HCV.

Indexed as

Apolipoproteins EApoptosis Regulatory ProteinsCell DeathGene SilencingHEK293 CellsHepacivirusHumansModels, BiologicalProtein BindingProtein DomainsProtein TransportRNA-Dependent RNA PolymeraseViral Nonstructural ProteinsVirionVirus InternalizationApolipoproteins EApoptosis Regulatory ProteinsCIDEB protein, humanNS-5 protein, hepatitis C virusRNA-Dependent RNA PolymeraseViral Nonstructural Proteins

Identifiers

PMID27282740
PMCPMC4901263
OpenAlexW2410570680

What OpenQuestion holds

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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.