Evidence map›Paper›PMID 38714690›Full record

ArticleNature communications2024

The genomic landscape of Vk*MYC myeloma highlights shared pathways of transformation between mice and humans.

Francesco Maura, David G Coffey, Caleb K Stein, Esteban Braggio, Bachisio Ziccheddu, Meaghen E Sharik, Megan T Du, Yuliza Tafoya Alvarado, Chang-Xin Shi, Yuan Xiao Zhu and 5 more

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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. B-cell-specificBlood neoplasia · 2025
    Article
  10. Review
  11. Chromoanagenesis in Multiple Myeloma: A Comprehensive Overview.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  12. Review
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Francesco Maura *Division of Myeloma, University of Miami, Miami, FL, USA. fxm557@med.miami.edu.ORCID http://orcid.org/0000-0002-5017-1620
David G Coffey *Division of Myeloma, University of Miami, Miami, FL, USA.ORCID http://orcid.org/0000-0003-3544-8836
Caleb K SteinDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.
Esteban BraggioDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0000-0003-3860-4830
Bachisio ZicchedduDivision of Myeloma, University of Miami, Miami, FL, USA.
Meaghen E SharikDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0009-0004-3128-4517
Megan T DuDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0000-0003-0486-4837
Yuliza Tafoya AlvaradoDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0009-0006-2626-1227
Chang-Xin ShiDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.
Yuan Xiao ZhuDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.
Erin W MeermeierDepartment of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0000-0002-9709-7624
Gareth J MorganMyeloma Research Program, NYU Langone, Perlmutter Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-4271-6360
Ola LandgrenDivision of Myeloma, University of Miami, Miami, FL, USA.ORCID http://orcid.org/0000-0001-6485-4839
P Leif Bergsagel *Department of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA.ORCID http://orcid.org/0000-0003-1523-7388
Marta Chesi *Department of Medicine, Division of Hematology and Medical Oncology, Mayo Clinic, Scottsdale, AZ, USA. chesi.marta@mayo.edu.ORCID http://orcid.org/0000-0002-4024-8225

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Yi Lin · 2015 to 2026
$25.5M
Tumor Biology Research ProgramP30CA240139 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Stephen D. Nimer · 2019 to 2026
$24.1M
Project 3 - Modeling Proteasome Inhibitor Response and Resistance in Cell Lines and Patient Samples with Single Cell Analysis of SubpopulationsU54CA224018 · NCI · MAYO CLINIC ARIZONA · PI BERGSAGEL, PETER LEIF · 2017 to 2021
$6.0M
Mayo Clinic Center for Clinical ProteomicsU01CA271410 · NCI · MAYO CLINIC ROCHESTER · PI Rafael Fonseca, AKHILESH PANDEY · 2022 to 2026
$5.3M
preclinical optimization of BCMA directed T cell therapyR01CA272426 · NCI · MAYO CLINIC ARIZONA · PI Peter Leif Bergsagel, Marta Chesi · 2023 to 2026
$2.5M
Credentialing a Genetically Engineered Clinically-Relevant Mouse Model of Multiple MyelomaR01CA234181 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2019 to 2023
$1.9M
NCI NIH HHS P30 CA240139NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA234181NCI NIH HHS R01 CA272426NCI NIH HHS U01 CA271410NCI NIH HHS U54 CA224018
6 · The paper itself

Abstract

Multiple myeloma (MM) is a heterogeneous disease characterized by frequent MYC translocations. Sporadic MYC activation in the germinal center of genetically engineered Vk*MYC mice is sufficient to induce plasma cell tumors in which a variety of secondary mutations are spontaneously acquired and selected over time. Analysis of 119 Vk*MYC myeloma reveals recurrent copy number alterations, structural variations, chromothripsis, driver mutations, apolipoprotein B mRNA-editing enzyme, catalytic polypeptide (APOBEC) mutational activity, and a progressive decrease in immunoglobulin transcription that inversely correlates with proliferation. Moreover, we identify frequent insertional mutagenesis by endogenous retro-elements as a murine specific mechanism to activate NF-kB and IL6 signaling pathways shared with human MM. Despite the increased genomic complexity associated with progression, advanced tumors remain dependent on MYC. In summary, here we credential the Vk*MYC mouse as a unique resource to explore MM genomic evolution and describe a fully annotated collection of diverse and immortalized murine MM tumors.

Indexed as

Multiple MyelomaProto-Oncogene Proteins c-mycAnimalsCell Transformation, NeoplasticDNA Copy Number VariationsGenomicsHumansMiceMice, TransgenicMutagenesis, InsertionalMutationNF-kappa BSignal TransductionTranslocation, GeneticNF-kappa BProto-Oncogene Proteins c-myc

Identifiers

PMID38714690
PMCPMC11076575

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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.