Evidence map›Paper›PMID 30872350›Full record

ArticleGenome research2019

A virome-wide clonal integration analysis platform for discovering cancer viral etiology.

Xun Chen, Jason Kost, Arvis Sulovari, Nathalie Wong, Winnie S Liang, Jian Cao, Dawei Li

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
–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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 57 citations in OpenAlex.

  1. Pooled it
  2. Gut virome dynamics: from commensal to critical player in health and disease.Nature reviews. Gastroenterology & hepatology · 2026
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  17. Revolutionized virome research using systems microbiology approaches.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
  18. Article
  19. Gut Virome: Role and Distribution in Health and Gastrointestinal Diseases.Frontiers in cellular and infection microbiology · 2022
    Review
  20. 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

7 authors at 4 institutions in 3 countries.

Xun ChenDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont 05405, USA.
Jason KostDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont 05405, USA.
Arvis SulovariDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont 05405, USA.
Nathalie WongDepartment of Anatomical and Cellular Pathology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, NT, Hong Kong 999077, P.R. China.
Winnie S LiangTranslational Genomics Research Institute, Phoenix, Arizona 85004, USA.
Jian CaoDivision of Medical Oncology, Rutgers Cancer Institute of New Jersey, Rutgers, The State University of New Jersey, New Brunswick, New Jersey 08903, USA.
Dawei LiDepartment of Microbiology and Molecular Genetics, University of Vermont, Burlington, Vermont 05405, USA.ORCID 0000-0002-9214-4487
University of Vermont · USChinese University of Hong Kong · HKRutgers, The State University of New Jersey · USTranslational Genomics Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncoviral infection is responsible for 12%-15% of cancer in humans. Convergent evidence from epidemiology, pathology, and oncology suggests that new viral etiologies for cancers remain to be discovered. Oncoviral profiles can be obtained from cancer genome sequencing data; however, widespread viral sequence contamination and noncausal viruses complicate the process of identifying genuine oncoviruses. Here, we propose a novel strategy to address these challenges by performing virome-wide screening of early-stage clonal viral integrations. To implement this strategy, we developed VIcaller, a novel platform for identifying viral integrations that are derived from any characterized viruses and shared by a large proportion of tumor cells using whole-genome sequencing (WGS) data. The sensitivity and precision were confirmed with simulated and benchmark cancer data sets. By applying this platform to cancer WGS data sets with proven or speculated viral etiology, we newly identified or confirmed clonal integrations of hepatitis B virus (HBV), human papillomavirus (HPV), Epstein-Barr virus (EBV), and BK Virus (BKV), suggesting the involvement of these viruses in early stages of tumorigenesis in affected tumors, such as HBV in

Indexed as

NeoplasmsVirus IntegrationWhole Genome SequencingBK VirusCarcinogenesisCell Transformation, NeoplasticDNA-Binding ProteinsDNA, ViralHepatitis B virusHerpesvirus 4, HumanHistone-Lysine N-MethyltransferaseHumansLiver NeoplasmsLymphoma, Non-HodgkinPapillomaviridaeSoftwareDNA-Binding ProteinsDNA, ViralHistone-Lysine N-MethyltransferaseKMT2B protein, human

Identifiers

PMID30872350
PMCPMC6499315
OpenAlexW2922069583

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.