Evidence map›Paper›PMID 31231470›Full record

ArticleOncotarget2019

Free episomal and integrated HBV DNA in HBsAg-negative patients with intrahepatic cholangiocarcinoma.

Teresa Pollicino, Cristina Musolino, Carlo Saitta, Gianluca Tripodi, Marika Lanza, Giuseppina Raffa, Francesca Casuscelli di Tocco, Chiara Raggi, Maria Consiglia Bragazzi, Adalberto Barbera and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. The role of HBV cccDNA in occult hepatitis B virus infection.Molecular and cellular biochemistry · 2023
    Review
  3. Occult hepatitis B virus infection in hepatitis C virus negative chronic liver diseases.Liver international : official journal of the International Association for the Study of the Liver · 2022
    Review
  4. 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

14 authors at 3 institutions in 1 country.

Teresa PollicinoDivision of Clinical and Molecular Hepatology, University Hospital of Messina, Italy.
Cristina MusolinoDepartment of Clinical and Experimental Medicine, University of Messina, Italy.
Carlo SaittaDivision of Clinical and Molecular Hepatology, University Hospital of Messina, Italy.
Gianluca TripodiDepartment of Clinical and Experimental Medicine, University of Messina, Italy.
Marika LanzaDepartment of Clinical and Experimental Medicine, University of Messina, Italy.
Giuseppina RaffaDivision of Clinical and Molecular Hepatology, University Hospital of Messina, Italy.
Francesca Casuscelli di ToccoDepartment of Clinical and Experimental Medicine, University of Messina, Italy.
Chiara RaggiHumanitas Research and Clinical Center, Rozzano, Milan, Italy.
Maria Consiglia BragazziDepartment of Translational and Precision Medicine, Sapienza University, Rome, Italy.
Adalberto BarberaDepartment of Human Pathology, University of Messina, Italy.
Giuseppe NavarraDepartment of Human Pathology, University of Messina, Italy.
Pietro InvernizziHumanitas Research and Clinical Center, Rozzano, Milan, Italy.
Domenico AlvaroDepartment of Translational and Precision Medicine, Sapienza University, Rome, Italy.
Giovanni RaimondoDivision of Clinical and Molecular Hepatology, University Hospital of Messina, Italy.
University of Messina · ITHumanitas University · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is evidence that chronic hepatitis B virus (HBV) infection is associated with an increased risk of intrahepatic cholangiocarcinoma (ICC) development, and it has been hypothesized an etiological role of HBV in the development of this tumor. Very little is known about occult HBV infection (OBI) in ICC. Aims of the study were to investigate the OBI prevalence and to characterize the HBV molecular status at intrahepatic level in OBI-positive cases with ICC. Frozen liver tumor specimens from 47 HBV surface-antigen-negative patients with ICC and 41 paired non-tumor liver tissues were tested for OBI by 4 different HBV-specific nested PCR. Covalently closed circular HBV DNA (HBV cccDNA) and viral integrations were investigated in OBI-positive cases. HBV DNA was detected in tumor and/or non-tumor specimens from 29/47 (61.7%) ICC patients. HBV cccDNA was found in tissues from 5/17 (34.5%) cases examined. HBV integration was detected in 4/10 (40%) tumor tissues tested and involved HBx and HBV-core gene sequences in 3 and 1 cases, respectively. Viral integration occurred: (a) 9,367 nucleotides upstream of the cat-eye-syndrome critical region protein-5-isoform coding sequence; (b) within the cystinosin isoform-1-precursor gene; (c) within the thromboxane-A-synthase-1 gene; (d) within the ATPase phospholipid transporting 9B gene. Occult HBV infection is highly prevalent in patients with ICC. Both free viral genomes and integrated HBV DNA can be present in these cases. These results suggest an involvement of HBV in the carcinogenic process leading to ICC development even in cases with occult infection.

Indexed as

covalently closed circular HBV DNAHBV DNA integrationhepatitis B virusintrahepatic cholangiocarcinomaoccult HBV Infection

Identifiers

PMID31231470
PMCPMC6570464
OpenAlexW2949466661

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.