Evidence map›Paper›PMID 25099228›Full record

ReviewHepatology (Baltimore, Md.)2015

Technical standards for hepatitis B virus X protein (HBx) research.

Betty L Slagle, Ourania M Andrisani, Michael J Bouchard, Caroline G L Lee, J-H James Ou, Aleem Siddiqui

Abstract readReview
In one paragraph

Review in Hepatology (Baltimore, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Relevance of HBx for Hepatitis B Virus-Associated Pathogenesis.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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.

Betty L SlagleDepartment of Molecular Virology & Microbiology, Baylor College of Medicine, Houston, TX.
Ourania M Andrisani
Michael J Bouchard
Caroline G L Lee
J-H James Ou
Aleem Siddiqui

Funding

Role of CREB/ATF Proteins in Hepatocyte Growth ControlR01DK044533 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI ANDRISANI, OURANIA M. · 1999 to 2021
$5.1M
Viral Hepatitis C and Lipid HomeostasisR01DK077704 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SIDDIQUI, ALEEM · 2008 to 2017
$3.0M
Role of Lipids in Hepatitis C Virus MaturationR01AI085087 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SIDDIQUI, ALEEM · 2010 to 2018
$2.9M
Hepatitis HBx-Mediated PathogenesisR01CA095388 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SLAGLE, BETTY L · 2003 to 2007
$1.5M
HBV replication and persistence in mouse modelsR01DK100257 · NIDDK · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2013 to 2016
$1.4M
Hepatitis C Virus-Induced Liver PathogenesisR01DK083479 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SIDDIQUI, ALEEM · 2010 to 2013
$1.3M
HBV replication and carcinogenesisR01CA177337 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2013 to 2015
$583k
Role of Lipids in Hepatitis C Virus MaturationR56AI085087 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SIDDIQUI, ALEEM · 2014 to 2014
$388k
Hepatitis B virus replication and DDB1R21CA177951 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SLAGLE, BETTY L · 2013 to 2014
$369k
SOMATOSTATIN GENE EXPRESSION--FUNCTIONAL DOMAINS OF CREBR29DK044533 · NIDDK · PURDUE UNIVERSITY WEST LAFAYETTE · PI ANDRISANI, OURANIA M. · 1993 to 1997
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NCI NIH HHS CA177337NCI NIH HHS R01 CA095388NCI NIH HHS R01 CA177337NCI NIH HHS R21 CA177951NIAID NIH HHS AI085087NIAID NIH HHS R01 AI085087NIAID NIH HHS R56 AI085087NIDDK NIH HHS DK044533NIDDK NIH HHS DK077704NIDDK NIH HHS DK083479NIDDK NIH HHS DK100257NIDDK NIH HHS R01 DK044533NIDDK NIH HHS R01 DK077704NIDDK NIH HHS R01 DK100257
6 · The paper itself

Abstract

Chronic infection with hepatitis B virus (HBV) is a risk factor for developing hepatocellular carcinoma (HCC). The life cycle of HBV is complex and has been difficult to study because HBV does not infect cultured cells. The HBV regulatory X protein (HBx) controls the level of HBV replication and possesses an HCC cofactor role. Attempts to understand the mechanism(s) that underlie HBx effects on HBV replication and HBV-associated carcinogenesis have led to many reported HBx activities that are likely influenced by the assays used. This review summarizes experimental systems commonly used to study HBx functions, describes limitations of these experimental systems that should be considered, and suggests approaches for ensuring the biological relevance of HBx studies.

Indexed as

Hepatitis B virusHumansLiver NeoplasmsResearch DesignTrans-ActivatorsViral Regulatory and Accessory ProteinsVirologyVirus Physiological Phenomenahepatitis B virus X proteinTrans-ActivatorsViral Regulatory and Accessory Proteins

Identifiers

PMID25099228
PMCPMC4320676

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.