Evidence map›Paper›PMID 42797762›Full record

ReviewViruses2026

Targeting cccDNA for Degradation: Endogenous- and Exogenous-Based Methods of Nuclear-Localized DNA Destruction in the Context of Chronic Hepatitis B Infection.

Cassie Thompson, Vanessa Meier-Stephenson

Abstract readReview
In one paragraph

Review in Viruses, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Cassie ThompsonDepartment of Medical Microbiology and Immunology, University of Alberta, Edmonton, AB T6G 2R3, Canada.ORCID 0009-0002-3591-1317
Vanessa Meier-StephensonDepartment of Medical Microbiology and Immunology, University of Alberta, Edmonton, AB T6G 2R3, Canada.ORCID 0000-0003-4004-4940

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability to facilitate cellular degradation or achieve therapeutic destruction of targeted noxious DNA is recognized as a major goal for the treatment of various viral infections. In the case of chronic hepatitis B, targeted DNA degradation of the episomal viral genome found in the nucleus of infected hepatocytes is key to achieving a true cure. However, mechanisms of targeted DNA degradation without excessive broadscale cytotoxicity are still under investigation by researchers. This review summarizes several current systems known to have the ability to target nuclear-localized DNA, including endogenous methods of DNA degradation that may be harnessed therapeutically and exogenous methods such as CRISPR or other xenobiotics, with a focus on their potential application in hepatitis B treatment.

Indexed as

Cell NucleusDNA, CircularDNA, ViralHepatitis B, ChronicHepatitis B virusAnimalsExtrachromosomal DNAHepatocytesHumansDNA, CircularDNA, ViralExtrachromosomal DNAAPOBECsapoptosiscccDNACRISPRendogenous DNA degradationhepatitis B virus (HBV)

Identifiers

PMID42797762
PMCPMC13611885

What Socratic 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 Socratic graph.