Evidence map›Paper›PMID 28486435›Full record

ReviewViruses2017

Regulated Entry of Hepatitis C Virus into Hepatocytes.

Zhijiang Miao, Zhenrong Xie, Jing Miao, Jieyu Ran, Yue Feng, Xueshan Xia

Abstract readReview
In one paragraph

Review in Viruses, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. A review of historical landmarks and pioneering technologies for the diagnosis of Hepatitis C Virus (HCV).European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Hepatitis C virus infection and tight junction proteins: The ties that bind.Biochimica et biophysica acta. Biomembranes · 2020
    Review
  14. Article
  15. Hepatitis C Virus Translation Regulation.International journal of molecular sciences · 2020
    Review
  16. The Role of the RNA-RNA Interactome in the Hepatitis C Virus Life Cycle.International journal of molecular sciences · 2020
    Review
  17. Tight Junction Proteins and the Biology of Hepatobiliary Disease.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Review
  20. 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

6 authors.

Zhijiang MiaoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China. miaozhijiang@yeah.net.
Zhenrong XieYunnan Institute of Digestive Disease, the First Affiliated Hospital of Kunming Medical University, Kunming 650032, China. xiezhenrong2006kycg@126.com.
Jing MiaoFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China. sanyue2016@yahoo.com.
Jieyu RanFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China. R6535930@126.com.
Yue FengFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China. fyky2005@163.com.
Xueshan XiaFaculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China. oliverxia2000@aliyun.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatitis C virus (HCV) is a model for the study of virus-host interaction and host cell responses to infection. Virus entry into hepatocytes is the first step in the HCV life cycle, and this process requires multiple receptors working together. The scavenger receptor class B type I (SR-BI) and claudin-1 (CLDN1), together with human cluster of differentiation (CD) 81 and occludin (OCLN), constitute the minimal set of HCV entry receptors. Nevertheless, HCV entry is a complex process involving multiple host signaling pathways that form a systematic regulatory network; this network is centrally controlled by upstream regulators epidermal growth factor receptor (EGFR) and transforming growth factor β receptor (TGFβ-R). Further feedback regulation and cell-to-cell spread of the virus contribute to the chronic maintenance of HCV infection. A comprehensive and accurate disclosure of this critical process should provide insights into the viral entry mechanism, and offer new strategies for treatment regimens and targets for HCV therapeutics.

Indexed as

Gene Expression RegulationHost-Pathogen InteractionsVirus InternalizationAntigens, CDClaudin-1ErbB ReceptorsHepacivirusHepatocytesHumansOccludinReceptors, Transforming Growth Factor betaScavenger Receptors, Class BSignal TransductionAntigens, CDClaudin-1EGFR protein, humanErbB ReceptorsOccludinReceptors, Transforming Growth Factor betaSCARB1 protein, humanScavenger Receptors, Class Bcell entryhepatitis C virusreceptorregulationsignaling

Identifiers

PMID28486435
PMCPMC5454413

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.