Evidence map›Paper›PMID 17182675›Full record

ArticleJournal of virology2007

Enhancement of hepatitis B virus replication by the regulatory X protein in vitro and in vivo.

Victor V Keasler, Amanda J Hodgson, Charles R Madden, Betty L Slagle

Abstract read
In one paragraph

Article in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing 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

82 citing papers in PubMed.

  1. Trial
  2. Identification ofFrontiers in immunology · 2018
    Trial
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. All-Viruses · 2023
    Article
  16. Relevance of HBx for Hepatitis B Virus-Associated Pathogenesis.International journal of molecular sciences · 2023
    Review
  17. Review
  18. Review
  19. Article
  20. Article

22 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

4 authors.

Victor V KeaslerDepartment of Molecular Virology and Microbiology, Baylor College of Medicine, BCM-385 One Baylor Plaza, Houston, TX 77030, USA.
Amanda J Hodgson
Charles R Madden
Betty L Slagle

Funding

Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Geoffrey A Preidis · 2001 to 2026
$28.3M
Hepatitis HBx-Mediated PathogenesisR01CA095388 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SLAGLE, BETTY L · 2003 to 2007
$1.5M
Hepatitis HBx-Mediated PathogenesisR56CA095388 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SLAGLE, BETTY L · 2009 to 2009
$300k
NCI NIH HHS CA 95388NCI NIH HHS R01 CA095388NCI NIH HHS R56 CA095388NIDDK NIH HHS DK 56338NIDDK NIH HHS P30 DK056338
6 · The paper itself

Abstract

The 3.2-kb hepatitis B virus (HBV) genome encodes a single regulatory protein termed HBx. While multiple functions have been identified for HBx in cell culture, its role in virus replication remains undefined. In the present study, we combined an HBV plasmid-based replication assay with the hydrodynamic tail vein injection model to investigate the function(s) of HBx in vivo. Using a greater-than-unit-length HBV plasmid DNA construct (payw1.2) and a similar construct with a stop codon at position 7 of the HBx open reading frame (payw1.2*7), we showed that HBV replication in transfected HepG2 cells was reduced 65% in the absence of HBx. These plasmids were next introduced into the livers of outbred ICR mice via hydrodynamic tail vein injection. At the peak of virus replication, at 4 days postinjection, intrahepatic markers of HBV replication were reduced 72% to 83% in mice injected with HBx-deficient payw1.2*7 compared to those measured in mice receiving wild-type payw1.2. A second plasmid encoding HBx was able to restore virus replication from payw1.2*7 to wild-type levels. Finally, viremia was monitored over the course of acute virus replication, and at 4 days postinjection, it was reduced by nearly 2 logs in the absence of HBx. These studies establish that the role for HBx in virus replication previously shown in transfected HepG2 cells is also apparent in the mouse liver within the context of acute hepatitis. Importantly, the function of HBx can now be studied in an in vivo setting that more closely approximates the cellular environment for HBV replication.

Indexed as

DNA ReplicationVirus ReplicationAnimalsAnimals, Outbred StrainsCarcinoma, HepatocellularCell Line, TumorDNA, ViralHepatitis B virusHumansImmunohistochemistryIn Vitro TechniquesLiverLiver NeoplasmsMiceMice, Inbred ICRPlasmidsDNA, Viralhepatitis B virus X proteinTrans-ActivatorsViral Regulatory and Accessory Proteins

Identifiers

PMID17182675
PMCPMC1865975

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.