Evidence map›Paper›PMID 25501510›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

Epstein-Barr virus latent antigens EBNA3C and EBNA1 modulate epithelial to mesenchymal transition of cancer cells associated with tumor metastasis.

Nivedita Gaur, Jaya Gandhi, Erle S Robertson, Subhash C Verma, Rajeev Kaul

Abstract read
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

27 citing papers in PubMed, 37 citations in OpenAlex.

  1. NEK2 drives pathogenesis, drug resistance, and LMP1 expression in EBV-positive non-Hodgkin lymphoma.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  12. Catching viral breast cancer.Infectious agents and cancer · 2021
    Review
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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 3 institutions in 2 countries.

Nivedita GaurDepartment of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi, 110021, India.
Jaya Gandhi
Erle S Robertson
Subhash C Verma
Rajeev Kaul
University of Delhi · INUniversity of Nevada, Reno · USUniversity of Pennsylvania · US

Funding

KSHV Lytic DNA Replication and its Control MechanismR01AI105000 · NIAID · UNIVERSITY OF NEVADA RENO · PI VERMA, SUBHASH C · 2013 to 2017
$1.8M
KSHV Genome Replication during Primary InfectionR01CA174459 · NCI · UNIVERSITY OF NEVADA RENO · PI VERMA, SUBHASH C · 2013 to 2017
$1.5M
Understanding the mechanism of KSHV latent DNA replicationR00CA126182 · NCI · UNIVERSITY OF NEVADA RENO · PI VERMA, SUBHASH C · 2009 to 2011
$740k
NCI NIH HHS CA174459NCI NIH HHS R00 CA126182NCI NIH HHS R01 CA174459NIAID NIH HHS AI105000NIAID NIH HHS R01 AI105000
6 · The paper itself

Abstract

Epithelial-mesenchymal transition is an important mechanism in cancer invasiveness and metastasis. We had previously reported that cancer cells expressing Epstein-Barr virus (EBV) latent viral antigens EBV nuclear antigen EBNA3C and/ or EBNA1 showed higher motility and migration potential and had a propensity for increased metastases when tested in nude mice model. We now show that both EBNA3C and EBNA1 can modulate cellular pathways critical for epithelial to mesenchymal transition of cancer cells. Our data confirms that presence of EBNA3C or EBNA1 result in upregulation of transcriptional repressor Slug and Snail, upregulation of intermediate filament of mesenchymal origin vimentin, upregulation of transcription factor TCF8/ZEB1, downregulation as well as disruption of tight junction zona occludens protein ZO-1, downregulation of cell adhesion molecule E-cadherin, and nuclear translocation of β-catenin. We further show that the primary tumors as well as metastasized lesions derived from EBV antigen-expressing cancer cells in nude mice model display EMT markers expression pattern suggesting their greater propensity to mesenchymal transition.

Indexed as

Epithelial-Mesenchymal TransitionAnimalsbeta CateninCadherinsEpstein-Barr Virus Nuclear AntigensGene Expression Regulation, NeoplasticHerpesvirus 4, HumanHomeodomain ProteinsHumansMiceNeoplasm MetastasisNeoplasmsSnail Family Transcription FactorsTranscription FactorsVimentinZinc Finger E-box-Binding Homeobox 1beta CateninCadherinsEBNA-3C, epstein-barr virusEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensHomeodomain ProteinsSNAI1 protein, humanSnai2 protein, mouseSnail Family Transcription FactorsTJP1 protein, humanTranscription FactorsVimentinZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1Zonula Occludens-1 Protein

Identifiers

PMID25501510
PMCPMC4793920
OpenAlexW2056688778

What OpenQuestion holds

Textmetadata
LicenceTDM
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.