Evidence map›Paper›PMID 40067173›Full record

ArticleBlood cancer discovery2025

Selective Enhancer Dependencies in MYC-Intact and MYC-Rearranged Germinal Center B-cell Diffuse Large B-cell Lymphoma.

Ashwin R Iyer, Aishwarya Gurumurthy, Shih-Chun A Chu, Rohan Kodgule, Athalee R Aguilar, Travis Saari, Abdullah Ramzan, Jan Rosa, Juhi Gupta, Arvind Emmanuel and 15 more

Abstract read
In one paragraph

Article in Blood cancer discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. CRISPR Interference to Inhibit Oncogenes for Cancer Therapy.International journal of molecular sciences · 2026
    Review
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors.

Ashwin R Iyer *Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-9846-8442
Aishwarya Gurumurthy *Department of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0003-0779-1434
Shih-Chun A ChuDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0003-3337-7421
Rohan KodguleDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-1711-8641
Athalee R AguilarDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-3522-2039
Travis SaariDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-8561-8317
Abdullah RamzanDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0009-0001-5776-316X
Jan RosaDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0009-0009-9886-3907
Juhi GuptaDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0003-4518-4221
Arvind EmmanuelDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0009-0009-7761-7379
Cody N HallDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-4601-4649
John S RungeDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-6489-8575
Anna B OwczarczykDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-9871-456X
Jang W ChoDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0009-0006-4712-9081
Matthew B WeissDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-6127-7626
Rockwell AnyohaBroad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts.ORCID 0000-0002-0363-3095
Kristin SikkinkArima Genomics, Carlsbad, California.ORCID 0000-0002-0805-0622
Savanna GemusArima Genomics, Carlsbad, California.ORCID 0009-0009-1058-8278
Charles P FulcoBroad Institute of Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts.ORCID 0000-0002-6592-1279
Anamarija M PerryDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-5700-2141
Anthony D SchmittArima Genomics, Carlsbad, California.ORCID 0000-0002-3818-1156
Jesse M EngreitzDepartment of Genetics, Stanford University School of Medicine, Stanford, California.ORCID 0000-0002-5754-1719
Noah A BrownDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-9151-5912
Marcin P CieslikDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0002-5467-1040
Russell J H RyanDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.ORCID 0000-0001-8174-3962

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Eric R. Fearon · 1988 to 2026
$178.2M
Identifying Functional Drivers of MYC Activation via Developmental Enhancers in Diffuse Large B-cell LymphomaR01CA245059 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RYAN, RUSSELL JAMES HUBBARD · 2020 to 2024
$1.7M
Systematic mapping and prediction of gene-enhancer connectionsR00HG009917 · NHGRI · STANFORD UNIVERSITY · PI ENGREITZ, JESSE M · 2020 to 2022
$796k
Oncogenic programs driven by Notch signaling in B-cell lymphomaK08CA208013 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RYAN, RUSSELL JAMES HUBBARD · 2016 to 2020
$791k
Systematic mapping and prediction of gene-enhancer connectionsK99HG009917 · NHGRI · BROAD INSTITUTE, INC. · PI ENGREITZ, JESSE M · 2018 to 2019
$65k
American Society of Hematology (ASH)Gordon and Betty Moore Foundation (GBMF)National Cancer Institute (NCI) K08-CA-208013National Human Genome Research Institute (NHGRI) K99HG009917NCI NIH HHS K08 CA208013NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA245059NHGRI NIH HHS K99 HG009917NHGRI NIH HHS R00 HG009917V Foundation for Cancer Research (VFCR) V2018-001
6 · The paper itself

Abstract

significanceAberrant MYC activity defines the most aggressive GCB-DLBCLs. We characterized a mechanism of MYC transcriptional activation via a native enhancer that is active in MYC-intact GCB-DLBCL, establishing fitness-sustaining cis- and trans-regulatory circuitry in GCB-DLBCL models that lack MYC enhancer-hijacking rearrangement. See related commentary by Mulet-Lazaro and Delwel, p. 149.

Indexed as

Enhancer Elements, GeneticGene RearrangementGerminal CenterLymphoma, Large B-Cell, DiffuseProto-Oncogene Proteins c-mycAnimalsGene Expression Regulation, NeoplasticHumansMiceMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID40067173
PMCPMC12050968

What Socratic holds

Textmetadata
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 Socratic graph.