Evidence map›Paper›PMID 38015841›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Nucleolin binds to and regulates transcription of hepatitis B virus covalently closed circular DNA minichromosome.

Yuchen Xia, Xiaoming Cheng, Tobias Nilsson, Min Zhang, Gaihong Zhao, Tadashi Inuzuka, Yan Teng, Yao Li, D Eric Anderson, Meghan Holdorf and 1 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Yuchen Xia *Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.ORCID 0000-0001-8460-3893
Xiaoming Cheng *Liver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.
Tobias NilssonDepartment of Infectious Diseases, Novartis Institutes for Biomedical Research, Emeryville, CA 94608.ORCID 0000-0001-5095-8493
Min ZhangLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.ORCID 0000-0003-3320-8150
Gaihong ZhaoState Key Laboratory of Virology and Hubei Province Key Laboratory of Allergy and Immunology, Institute of Medical Virology, TaiKang Center for Life and Medical Sciences, TaiKang Medical School, Wuhan University, Wuhan 430071, China.
Tadashi InuzukaLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.
Yan TengState Key Laboratory of Virology and Hubei Province Key Laboratory of Allergy and Immunology, Institute of Medical Virology, TaiKang Center for Life and Medical Sciences, TaiKang Medical School, Wuhan University, Wuhan 430071, China.
Yao LiLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.
D Eric AndersonAdvanced Mass Spectrometry Core, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.ORCID 0000-0002-6838-0201
Meghan HoldorfDepartment of Infectious Diseases, Novartis Institutes for Biomedical Research, Emeryville, CA 94608.
T Jake LiangLiver Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, NIH, Bethesda, MD 20892.ORCID 0000-0003-3828-702X
National Institute of Diabetes and Digestive and Kidney Diseases · USWuhan University · CNNovartis (United States) · US

Funding

MOLECULAR MECHANISMS IN RENAL INTERSTITIAL FIBROSISR01DK054500 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI EDDY, ALLISON AUDREY · 1999 to 2008
$2.8M
MOLECULAR MECHANISMS OF HEPATITIS B VIRAL PATHOGENESIS AND PERSISTENCEZ01DK054500 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI LIANG, T. JAKE · 1997 to 2008
$927k
Intramural NIH HHS Z01 DK054500NIDDK NIH HHS R01 DK054500
6 · The paper itself

Abstract

Hepatitis B virus (HBV) remains a major public health threat with nearly 300 million people chronically infected worldwide who are at a high risk of developing hepatocellular carcinoma. Current therapies are effective in suppressing HBV replication but rarely lead to cure. Current therapies do not affect the HBV covalently closed circular DNA (cccDNA), which serves as the template for viral transcription and replication and is highly stable in infected cells to ensure viral persistence. In this study, we aim to identify and elucidate the functional role of cccDNA-associated host factors using affinity purification and protein mass spectrometry in HBV-infected cells. Nucleolin was identified as a key cccDNA-binding protein and shown to play an important role in HBV cccDNA transcription, likely via epigenetic regulation. Targeting nucleolin to silence cccDNA transcription in infected hepatocytes may be a promising therapeutic strategy for a functional cure of HBV.

Indexed as

Hepatitis BLiver NeoplasmsDNA, CircularDNA, ViralEpigenesis, GeneticHepatitis B virusHumansNucleolinVirus ReplicationDNA, CircularDNA, ViralNucleolinantiviralepigeneticsHBV minichromosomeproteomicsviral replication

Identifiers

PMID38015841
PMCPMC10710063
OpenAlexW4389100355

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.