Evidence map›Paper›PMID 33836152›Full record

ArticleCancer cell2021

Oncogenic extrachromosomal DNA functions as mobile enhancers to globally amplify chromosomal transcription.

Yanfen Zhu, Amit D Gujar, Chee-Hong Wong, Harianto Tjong, Chew Yee Ngan, Liang Gong, Yi-An Chen, Hoon Kim, Jihe Liu, Meihong Li and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 186 papers.

0numbers the graph read from it
0cells of the map it votes in
186citing papers in PubMed
18.9field-weighted citation impact, top 1% 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

186 citing papers in PubMed, 276 citations in OpenAlex.

  1. Review
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  9. Examining the role of extrachromosomal DNA in lung cancer.Journal of the National Cancer Institute · 2026
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  19. Targeting extrachromosomal DNA in human cancers.Nature reviews. Drug discovery · 2026
    Review
  20. Article

126 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 2 institutions in 1 country.

Yanfen ZhuThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Amit D GujarThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Chee-Hong WongThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Harianto TjongThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Chew Yee NganThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Liang GongThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Yi-An ChenThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Hoon KimThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Jihe LiuThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Meihong LiThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Adam Mil-HomensThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Rahul MauryaThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Chris KuhlbergThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Fanyue SunThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Eunhee YiThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Ana C deCarvalhoDepartment of Neurosurgery, Henry Ford Hospital, Detroit, MI 48202, USA.
Yijun RuanThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA.
Roel G W VerhaakThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA. Electronic address: roel.verhaak@jax.org.
Chia-Lin WeiThe Jackson Laboratory for Genomic Medicine, Farmington, CT 06032, USA. Electronic address: chia-lin.wei@jax.org.
Jackson Laboratory · USHenry Ford Hospital · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Comprehensive Mapping of Long-Range Chromatin Interactions in Humanand Mouse GenomesUM1HG009409 · NHGRI · JACKSON LABORATORY · PI LEE, CHARLES · 2017 to 2021
$9.8M
Nucleome Positioning System for Spatiotemporal Genome Organization and RegulationU54DK107967 · NIDDK · JACKSON LABORATORY · PI WEI, CHIA-LIN · 2015 to 2019
$3.6M
Extrachromosomal DNA as a Targetable Mechanism in GlioblastomaR01CA237208 · NCI · YALE UNIVERSITY · PI VERHAAK, ROEL GW · 2020 to 2024
$2.5M
Development of Single Molecule Chromatin Interaction Assays (smChIA) in Single NucleiR01GM127531 · NIGMS · JACKSON LABORATORY · PI WEI, CHIA-LIN · 2019 to 2022
$2.3M
Advancing Ultra Long-read Sequencing and Chromatin Interaction Analyses for Chromosomal and Extrachromosomal Structural Variation Characterization in CancerR33CA236681 · NCI · JACKSON LABORATORY · PI VERHAAK, ROEL GW, WEI, CHIA-LIN · 2020 to 2020
$1.4M
(PQ #4) Single cell barcoding for studies of study clonal evolution in glioblastomaR01CA190121 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SULMAN, ERIK, VERHAAK, ROEL GW · 2014 to 2017
$1.4M
Modeling Tumor Evolution in GliomaR21NS114873 · NINDS · JACKSON LABORATORY · PI VERHAAK, ROEL GW · 2019 to 2020
$520k
NCI NIH HHS P30 CA034196NCI NIH HHS R01 CA190121NCI NIH HHS R01 CA237208NCI NIH HHS R33 CA236681NHGRI NIH HHS UM1 HG009409NIDDK NIH HHS U54 DK107967NIGMS NIH HHS R01 GM127531NINDS NIH HHS R21 NS114873
6 · The paper itself

Abstract

Extrachromosomal, circular DNA (ecDNA) is emerging as a prevalent yet less characterized oncogenic alteration in cancer genomes. We leverage ChIA-PET and ChIA-Drop chromatin interaction assays to characterize genome-wide ecDNA-mediated chromatin contacts that impact transcriptional programs in cancers. ecDNAs in glioblastoma patient-derived neurosphere and prostate cancer cell cultures are marked by widespread intra-ecDNA and genome-wide chromosomal interactions. ecDNA-chromatin contact foci are characterized by broad and high-level H3K27ac signals converging predominantly on chromosomal genes of increased expression levels. Prostate cancer cells harboring synthetic ecDNA circles composed of characterized enhancers result in the genome-wide activation of chromosomal gene transcription. Deciphering the chromosomal targets of ecDNAs at single-molecule resolution reveals an association with actively expressed oncogenes spatially clustered within ecDNA-directed interaction networks. Our results suggest that ecDNA can function as mobile transcriptional enhancers to promote tumor progression and manifest a potential synthetic aneuploidy mechanism of transcription control in cancer.

Indexed as

CarcinogenesisChromatinChromosomesDNA, NeoplasmGlioblastomaHumansOncogenesChromatinDNA, NeoplasmChIA-DropChIA-PETchromatin interactionsecDNAmobile enhancers

Identifiers

PMID33836152
PMCPMC8119378
OpenAlexW3146078726

What OpenQuestion holds

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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.