Evidence map›Paper›PMID 34066744›Full record

ReviewViruses2021

Hepatitis B Virus Pre-S Gene Deletions and Pre-S Deleted Proteins: Clinical and Molecular Implications in Hepatocellular Carcinoma.

Yueh-Te Lin, Long-Bin Jeng, Wen-Ling Chan, Ih-Jen Su, Chiao-Fang Teng

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 20 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

5 authors at 4 institutions in 1 country.

Yueh-Te LinCancer Genome Research Center, Chang Gung Memorial Hospital, Taoyuan 333, Taiwan.
Long-Bin JengOrgan Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.
Wen-Ling ChanDepartment of Bioinformatics and Medical Engineering, Asia University, Taichung 413, Taiwan.
Ih-Jen SuDepartment of Biotechnology, Southern Taiwan University of Science and Technology, Tainan 710, Taiwan.
Chiao-Fang TengOrgan Transplantation Center, China Medical University Hospital, Taichung 404, Taiwan.ORCID 0000-0002-5218-0571
China Medical University · TWAsia University · TWChang Gung Memorial Hospital · TWSouthern Taiwan University of Science and Technology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most frequent and fatal human cancers worldwide and its development and prognosis are intimately associated with chronic infection with hepatitis B virus (HBV). The identification of genetic mutations and molecular mechanisms that mediate HBV-induced tumorigenesis therefore holds promise for the development of potential biomarkers and targets for HCC prevention and therapy. The presence of HBV pre-S gene deletions in the blood and the expression of pre-S deleted proteins in the liver tissues of patients with chronic hepatitis B and HBV-related HCC have emerged as valuable biomarkers for higher incidence rates of HCC development and a higher risk of HCC recurrence after curative surgical resection, respectively. Moreover, pre-S deleted proteins are regarded as important oncoproteins that activate multiple signaling pathways to induce DNA damage and promote growth and proliferation in hepatocytes, leading to HCC development. The signaling molecules dysregulated by pre-S deleted proteins have also been validated as potential targets for the prevention of HCC development. In this review, we summarize the clinical and molecular implications of HBV pre-S gene deletions and pre-S deleted proteins in HCC development and recurrence and highlight their potential applications in HCC prevention and therapy.

Indexed as

Gene DeletionAnimalsBiomarkersCarcinoma, HepatocellularCell CycleCell Transformation, ViralCentrosomeDisease Models, AnimalDisease SusceptibilityDNA DamageEndoplasmic Reticulum StressGene Expression Regulation, ViralHepatitis BHepatitis B Surface AntigensHepatitis B virusHumansBiomarkersHepatitis B Surface Antigensbiomarkershepatitis B virushepatocellular carcinomapre-S deleted proteinspre-S gene deletionstargets

Identifiers

PMID34066744
PMCPMC8151789
OpenAlexW3163276578

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.