Evidence map›Paper›PMID 35015307›Full record

ArticleAmerican journal of hematology2022

PD-L1 overexpression correlates with JAK2-V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms.

Jelena D Milosevic Feenstra, Roland Jäger, Fiorella Schischlik, Daniel Ivanov, Gregor Eisenwort, Elisa Rumi, Michael Schuster, Bettina Gisslinger, Sigrid Machherndl-Spandl, Peter Bettelheim and 7 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Homozygosity of germ lineBlood neoplasia · 2026
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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

17 authors at 6 institutions in 3 countries.

Jelena D Milosevic FeenstraLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-7420-3298
Roland JägerDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Fiorella SchischlikCancer Data Science Laboratory, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, USA.
Daniel IvanovDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Gregor EisenwortLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Elisa RumiDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.ORCID 0000-0002-7572-9504
Michael SchusterCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Bettina GisslingerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
Sigrid Machherndl-SpandlDepartment of Haematology, Internal Oncology and Stem Cell Transplantation, Ordensklinikum Linz Elisabethinen Hospital, Linz, Austria.
Peter BettelheimDepartment of Haematology, Internal Oncology and Stem Cell Transplantation, Ordensklinikum Linz Elisabethinen Hospital, Linz, Austria.
Maria-Theresa KrauthLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Felix KeilLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Christoph BockCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Mario CazzolaDepartment of Molecular Medicine, University of Pavia, Pavia, Italy.
Heinz GisslingerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-0295-7629
Robert KralovicsDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-6997-8539
Peter ValentLudwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATAustrian Academy of Sciences · ATKrankenhaus der Elisabethinen · ATUniversity of Pavia · ITHanusch Hospital · ATNational Cancer Institute · US

Funding

Austrian Science Fund FWF P 34451
6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPN) are chronic stem cell disorders characterized by enhanced proliferation of myeloid cells, immune deregulation, and drug resistance. JAK2 somatic mutations drive the disease in 50-60% and CALR mutations in 25-30% of cases. Published data suggest that JAK2-V617F-mutated MPN cells express the resistance-related checkpoint PD-L1. By applying RNA-sequencing on granulocytes of 113 MPN patients, we demonstrate that PD-L1 expression is highest among polycythemia vera patients and that PD-L1 expression correlates with JAK2-V617F mutational burden (R = 0.52; p < .0001). Single nucleotide polymorphism (SNP) arrays showed that chromosome 9p uniparental disomy (UPD) covers both PD-L1 and JAK2 in all MPN patients examined. MPN cells in JAK2-V617F-positive patients expressed higher levels of PD-L1 if 9p UPD was present compared to when it was absent (p < .0001). Moreover, haplotype-based association analyses provided evidence for germline genetic factors at PD-L1 locus contributing to MPN susceptibility independently of the previously described GGCC risk haplotype. We also found that PD-L1 is highly expressed on putative CD34

Indexed as

B7-H1 AntigenMyeloproliferative DisordersPolycythemia VeraUniparental DisomyBromodomain Containing ProteinsCell Cycle ProteinsHumansJanus Kinase 2MutationNuclear ProteinsTranscription FactorsB7-H1 AntigenBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsJAK2 protein, humanJanus Kinase 2Nuclear ProteinsTranscription Factors

Identifiers

PMID35015307
PMCPMC9306481
OpenAlexW4206045901

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.