Evidence map›Paper›PMID 37333202›Full record

ArticlebioRxiv : the preprint server for biology2023

Locus specific human endogenous retroviruses reveal new lymphoma subtypes.

Bhavya Singh, Nicholas Dopkins, Tongyi Fei, Jez L Marston, Stephanie Michael, Helena Reyes-Gopar, Gislaine Curty, Jonas J Heymann, Amy Chadburn, Peter Martin and 4 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. 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, 6 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 3 countries.

Bhavya SinghDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Nicholas DopkinsDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Tongyi FeiDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Jez L MarstonDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Stephanie MichaelDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Helena Reyes-GoparPrograma de Doctorado en Ciencias Biomédicas, Universidad Nacional Autónoma de México, Mexico City, Mexico.
Gislaine CurtyBrazilian National Cancer Institute (INCA), Rio de Janeiro, Brazil.
Jonas J HeymannDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Amy ChadburnDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Peter MartinDivision of Hematology and Medical Oncology, Weill Cornell Medicine, New York, NY, USA.
Fabio E LealBrazilian National Cancer Institute (INCA), Rio de Janeiro, Brazil.
Ethel CesarmanDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY, USA.
Douglas F NixonDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Matthew L BendallDivision of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, NY, USA.
Cornell University · USInstituto Nacional de Câncer - INCA · BRNational Institute of Genomic Medicine · MX

Funding

Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
Regulatory Crosstalk Between Human Endogenous Retroviruses, HIV, and EBV, in LymphomaR01CA260691 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CESARMAN, ETHEL, NIXON, DOUGLAS F · 2021 to 2025
$5.8M
NCI NIH HHS R01 CA260691NIGMS NIH HHS T32 GM007739
6 · The paper itself

Abstract

The heterogeneity of cancers are driven by diverse mechanisms underlying oncogenesis such as differential 'cell-of-origin' (COO) progenitors, mutagenesis, and viral infections. Classification of B-cell lymphomas have been defined by considering these characteristics. However, the expression and contribution of transposable elements (TEs) to B cell lymphoma oncogenesis or classification have been overlooked. We hypothesized that incorporating TE signatures would increase the resolution of B-cell identity during healthy and malignant conditions. Here, we present the first comprehensive, locus-specific characterization of TE expression in benign germinal center (GC) B-cells, diffuse large B-cell lymphoma (DLBCL), Epstein-Barr virus (EBV)-positive and EBV-negative Burkitt lymphoma (BL), and follicular lymphoma (FL). Our findings demonstrate unique human endogenous retrovirus (HERV) signatures in the GC and lymphoma subtypes whose activity can be used in combination with gene expression to define B-cell lineage in lymphoid malignancies, highlighting the potential of retrotranscriptomic analyses as a tool in lymphoma classification, diagnosis, and the identification of novel treatment groups.

Identifiers

PMID37333202
PMCPMC10274920
OpenAlexW4379927843

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.