Evidence map›Paper›PMID 36325353›Full record

ReviewFrontiers in immunology2022

Role of epigenetic modification in interferon treatment of hepatitis B virus infection.

Zhijing Yang, Baozhen Sun, Jingcheng Xiang, Han Wu, Shaoning Kan, Ming Hao, Lu Chang, Huimin Liu, Dongxu Wang, Weiwei Liu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Oncogenic viruses rewire the epigenome in human cancer.Frontiers in cellular and infection microbiology · 2025
    Review
  8. Article
  9. [Therapeutic strategies, practice, and prospect of a clinical cure for chronic hepatitis B in China].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Article
  10. Review
  11. Article
  12. Review
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

10 authors at 1 institution in 1 country.

Zhijing YangDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Baozhen SunDepartment of Hepatobiliary and Pancreas Surgery, China-Japan Union Hospital of Jilin University, Changchun, China.
Jingcheng XiangDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Han WuDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Shaoning KanDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Ming HaoDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Lu ChangDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Huimin LiuDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Dongxu WangLaboratory Animal Center, College of Animal Science, Jilin University, Changchun, China.
Weiwei LiuDepartment of Oral and Maxillofacial Surgery, Hospital of Stomatology, Jilin University, Changchun, China.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human hepatitis B virus (HBV) is a small, enveloped DNA virus that causes acute and chronic hepatitis. Chronic hepatitis B (CHB) is associated with hepatocellular carcinoma pathogenesis. Interferons (IFNs) have been used for the treatment of CHB for a long time, with advantages including less treatment duration and sustained virological response. Presently, various evidence suggests that epigenetic modification of the viral covalently closed circular DNA (cccDNA) and the host genome is crucial for the regulation of viral activity. This modification includes histone acetylation, DNA methylation, N6-methyladenosine, and non-coding RNA modification. IFN treatment for CHB can stimulate multiple IFN-stimulated genes for inhibiting virus replication. IFNs can also affect the HBV life cycle through epigenetic modulation. In this review, we summarized the different mechanisms through which IFN-α inhibits HBV replication, including epigenetic regulation. Moreover, the mechanisms underlying IFN activity are discussed, which indicated its potential as a novel treatment for CHB. It is proposed that epigenetic changes such as histone acetylation, DNA methylation, m6A methylation could be the targets of IFN, which may offer a novel approach to HBV treatment.

Indexed as

Hepatitis BHepatitis B virusAntiviral AgentsDNA, ViralEpigenesis, GeneticHistonesHumansInterferon-alphaAntiviral AgentsDNA, ViralHistonesInterferon-alphaCccDNAepigenetic regulationHBVIFN therapyISGs

Identifiers

PMID36325353
PMCPMC9618964
OpenAlexW4306392320

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.