Evidence map›Paper›PMID 39277592›Full record

ArticleNature communications2024

Enhancer-promoter hubs organize transcriptional networks promoting oncogenesis and drug resistance.

Brent S Perlman, Noah Burget, Yeqiao Zhou, Gregory W Schwartz, Jelena Petrovic, Zora Modrusan, Robert B Faryabi

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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  4. Role ofZoological research · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Brent S Perlman *Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.ORCID 0009-0003-0147-3731
Noah Burget *Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.
Yeqiao ZhouDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA.
Gregory W SchwartzPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.ORCID 0000-0003-4003-3045
Jelena PetrovicDepartment of Proteomic and Genomic Technologies, Genentech, South San Francisco, USA.
Zora ModrusanDepartment of Proteomic and Genomic Technologies, Genentech, South San Francisco, USA.
Robert B FaryabiDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, USA. faryabi@pennmedicine.upenn.edu.ORCID 0000-0002-7931-2175

Funding

Notch-driven Epigenetic Program of MYC and CCND1 in Triple-Negative Breast CancerR01CA230800 · NCI · UNIVERSITY OF PENNSYLVANIA · PI FARYABI, ROBERT BABAK · 2020 to 2025
$2.1M
Epigenetic Mechanisms Underpinning Mantle Cell Lymphoma Sensitivity and Resistance to Notch InhibitorsR01CA248041 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Robert Babak Faryabi · 2022 to 2026
$2.1M
NCI NIH HHS R01 CA230800NCI NIH HHS R01 CA248041U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-CA230800U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-CA248041
6 · The paper itself

Abstract

Recent advances in high-resolution mapping of spatial interactions among regulatory elements support the existence of complex topological assemblies of enhancers and promoters known as enhancer-promoter hubs or cliques. Yet, organization principles of these multi-interacting enhancer-promoter hubs and their potential role in regulating gene expression in cancer remain unclear. Here, we systematically identify enhancer-promoter hubs in breast cancer, lymphoma, and leukemia. We find that highly interacting enhancer-promoter hubs form at key oncogenes and lineage-associated transcription factors potentially promoting oncogenesis of these diverse cancer types. Genomic and optical mapping of interactions among enhancer and promoter elements further show that topological alterations in hubs coincide with transcriptional changes underlying acquired resistance to targeted therapy in T cell leukemia and B cell lymphoma. Together, our findings suggest that enhancer-promoter hubs are dynamic and heterogeneous topological assemblies with the potential to control gene expression circuits promoting oncogenesis and drug resistance.

Indexed as

CarcinogenesisDrug Resistance, NeoplasmEnhancer Elements, GeneticGene Expression Regulation, NeoplasticGene Regulatory NetworksPromoter Regions, GeneticBreast NeoplasmsCell Line, TumorFemaleHumansLeukemiaLymphomaOncogenesTranscription FactorsTranscription Factors

Identifiers

PMID39277592
PMCPMC11401928

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LicenceCC BY-NC-ND
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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.