Evidence map›Paper›PMID 41279324›Full record

ArticlebioRxiv : the preprint server for biology2025

Single-Cell Profiling of HDAC Inhibitor-Induced EBV Lytic Heterogeneity Defines Abortive and Refractory States in B Lymphoblasts.

Lauren E Haynes, Ashley P Barry, Micah A Luftig

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Lauren E HaynesDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Duke Center for Virology, Durham, NC, USA.
Ashley P BarryDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Duke Center for Virology, Durham, NC, USA.
Micah A LuftigDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Duke Center for Virology, Durham, NC, USA.ORCID 0000-0002-2964-1907

Funding

Viral Oncology Training GrantT32CA009111 · NCI · DUKE UNIVERSITY · PI LUFTIG, MICAH A. · 1985 to 2023
$8.9M
Targeting Apoptosis and Immune Control of Epstein-Barr Virus Infected Tonsillar B CellsR01DE025994 · NIDCR · DUKE UNIVERSITY · PI Micah Alan Luftig · 2016 to 2026
$5.0M
Defining and exploiting EBV-infected cell heterogeneity in non-Hodgkin lymphomasU01CA275306 · NCI · DUKE UNIVERSITY · PI Micah Alan Luftig · 2022 to 2026
$3.0M
Defining host mechanisms that restrict EBV lytic reactivationF31DE033216 · NIDCR · DUKE UNIVERSITY · PI HAYNES, LAUREN · 2023 to 2025
$128k
NCI NIH HHS T32 CA009111NCI NIH HHS U01 CA275306NIDCR NIH HHS F31 DE033216NIDCR NIH HHS R01 DE025994
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) is associated with multiple malignancies including Burkitt lymphoma (BL), Hodgkin's lymphomas, nasopharyngeal carcinomas (NPC), and gastric cancers. Canonically, EBV positive tumors display latent gene expression programs that are difficult to target pharmacologically. To overcome this hurdle, lytic reactivation therapies have been developed based on HDAC inhibition with limited mechanistic studies. We therefore characterized the impact of pan-HDAC inhibitor, panobinostat, and class I HDAC inhibitor, nanatinostat, on the growth, survival, and lytic reactivation of four EBV-positive cell lines: P3HR1-ZHT BL, Jijoye BL, IBL-1 immunoblastic lymphoma, and

Identifiers

PMID41279324
PMCPMC12632546

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Registered trials

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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.