Evidence map›Paper›PMID 34921959›Full record

ArticleExperimental hematology2022

Transcriptional differences between JAK2-V617F and wild-type bone marrow cells in patients with myeloproliferative neoplasms.

Debra Van Egeren, Baransel Kamaz, Shichen Liu, Maximilian Nguyen, Christopher R Reilly, Maria Kalyva, Daniel J DeAngelo, Ilene Galinsky, Martha Wadleigh, Eric S Winer and 8 more

Open access · greenAbstract read
In one paragraph

Article in Experimental hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Macrophages in Hematopoiesis and Related Blood Diseases.Genomics, proteomics & bioinformatics · 2025
    Review
  5. Article
  6. Monocyte Involvement in the Pathogenesis of Myeloproliferative Neoplasms.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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  15. Review
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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

18 authors at 5 institutions in 2 countries.

Debra Van EgerenDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA; Department of Systems Biology, Harvard Medical School, Boston, MA; Stem Cell Program, Boston Children's Hospital, Boston, MA.
Baransel KamazDivision of Hematology, Brigham and Women's Hospital, Boston, MA.
Shichen LiuDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA.
Maximilian NguyenDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA; Department of Systems Biology, Harvard Medical School, Boston, MA.
Christopher R ReillyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Maria KalyvaEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
Daniel J DeAngeloDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Ilene GalinskyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Martha WadleighDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Eric S WinerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Marlise R LuskinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Richard M StoneDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Jacqueline S GarciaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Gabriela S HobbsLeukemia Center, Massachusetts General Hospital, Boston, MA.
Franziska MichorDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA; Broad Institute of MIT and Harvard, Cambridge, MA; Department of Biostatistics, Harvard T. H. Chan School of Public Health, Boston, MA; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA; The Center for Cancer Evolution, Dana-Farber Cancer Institute, Boston, MA; The Ludwig Center at Harvard, Boston, MA.
Isidro Cortes-CirianoEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK. Electronic address: icortes@ebi.ac.uk.
Ann MullallyDivision of Hematology, Brigham and Women's Hospital, Boston, MA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA; Broad Institute of MIT and Harvard, Cambridge, MA. Electronic address: Ann_Mullally@dfci.harvard.edu.
Sahand HormozDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA; Department of Systems Biology, Harvard Medical School, Boston, MA; Broad Institute of MIT and Harvard, Cambridge, MA. Electronic address: sahand_hormoz@hms.harvard.edu.
Dana-Farber Cancer Institute · USEuropean Bioinformatics Institute · GBBrigham and Women's Hospital · USBroad Institute · USMassachusetts General Hospital · US

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI HOLLAND, ERIC C., MICHOR, FRANZISKA · 2015 to 2020
$11.2M
Targeting SYK Kinase in AMLP50CA206963 · NCI · DANA-FARBER CANCER INST · PI STEGMAIER, KIMBERLY · 2017 to 2021
$10.6M
Training Program in Molecular HematologyT32HL116324 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI NANCY BERLINER · 2013 to 2026
$7.4M
Functional and Molecular Dissection of Mutant Calreticulin in Myeloproliferative NeoplasmsR01HL131835 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI Ann Mullally · 2016 to 2026
$4.1M
Tracing the lineage histories and differentiation trajectories of individual cancer cells in myeloproliferative neoplasmsR01HL158269 · NHLBI · DANA-FARBER CANCER INST · PI HORMOZ, SAHAND · 2021 to 2025
$2.3M
Lineage-based inference of cell state transition dynamics in development and diseaseR00GM118910 · NIGMS · DANA-FARBER CANCER INST · PI HORMOZ, SAHAND · 2017 to 2019
$747k
NCI NIH HHS P01 CA066996NCI NIH HHS P50 CA206963NCI NIH HHS U54 CA193461NHLBI NIH HHS R01 HL131835NHLBI NIH HHS R01 HL158269NHLBI NIH HHS T32 HL116324NIGMS NIH HHS R00 GM118910
6 · The paper itself

Abstract

The JAK2-V617F mutation is the most common cause of myeloproliferative neoplasms. Although experiments have revealed that this gain-of-function mutation is associated with myeloid blood cell expansion and increased production of white cells, red cells, and platelets, the transcriptional consequences of the JAK2-V617F mutation in different cellular compartments of the bone marrow have not yet been fully elucidated. To study the direct effects of JAK2-V617F on bone marrow cells in patients with myeloproliferative neoplasms, we performed joint single-cell RNA sequencing and JAK2 genotyping on CD34

Indexed as

Myeloproliferative DisordersPolycythemia VeraThrombocythemia, EssentialBone Marrow CellsHumansJanus Kinase 2MutationJAK2 protein, humanJanus Kinase 2

Identifiers

PMID34921959
PMCPMC9332124
OpenAlexW4200542746

What OpenQuestion holds

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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.