Evidence map›Paper›PMID 33599741›Full record

ArticleBlood advances2021

Patients with triple-negative, JAK2V617F- and CALR-mutated essential thrombocythemia share a unique gene expression signature.

Samah Alimam, William Villiers, Richard Dillon, Michael Simpson, Manohursingh Runglall, Alexander Smith, Prodromos Chatzikyriakou, Paul Lavender, Anju Kanda, Ken Mills and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Blood advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Platelet Disorders and Medication Strategies.Thrombosis and haemostasis · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 2 countries.

Samah AlimamDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
William VilliersDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Richard DillonDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Michael SimpsonDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Manohursingh RunglallNIHR Comprehensive Biomedical Research Centre at Guy's and St. Thomas' NHS Foundation Trust in partnership with King's College London and King's College Hospital, London, United Kingdom.
Alexander SmithDepartment of Haematology, King's College NHS Trust, London, United Kingdom.
Prodromos ChatzikyriakouGenetics and Molecular Medicine Research Division, King's College London, London, United Kingdom.
Paul LavenderSchool of Immunology & Microbial Sciences, MRC and Asthma UK Centre in Allergic Mechanisms of Asthma, King's College London, London, United Kingdom.
Anju KandaDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Ken MillsCentre for Cancer Research and Cell Biology, Queen's University, Belfast, United Kingdom.
Beatriz Bellosillo ParicioLaboratori de Diagnòstic Molecular, Servei de Patologia, Hospital del Mar, Barcelona, Spain; and.
James Kaufman-CookDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Sophie OrdDepartment of Medical and Molecular Genetics, King's College London, London, United Kingdom.
Shahram KordastiDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Deepti RadiaDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Claire WoodleyDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Yvonne FrancisDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Ghulam MuftiDepartment of Haematology, King's College NHS Trust, London, United Kingdom.
Donal P McLornanDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
Claire N HarrisonDepartment of Haematology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.
King's College London · GBGuy's and St Thomas' NHS Foundation Trust · GBKing's College Hospital NHS Foundation Trust · GBHospital Del Mar · ESQueen's University Belfast · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately 10% to 15% of patients with essential thrombocythemia (ET) lack the common driver mutations, so-called "triple-negative" (TN) disease. We undertook a systematic approach to investigate for somatic mutations and delineate gene expression signatures in 46 TN patients and compared the results to those with known driver mutations and healthy volunteers. Deep, error-corrected, next-generation sequencing of peripheral blood mononuclear cells using the HaloPlexHS platform and whole-exome sequencing was performed. Using this platform, 10 (22%) of 46 patients had detectable mutations (MPL, n = 6; JAK2V617F, n = 4) with 3 of 10 cases harboring germline MPL mutations. RNA-sequencing and DNA methylation analysis were also performed by using peripheral blood mononuclear cells. Pathway analysis comparing healthy volunteers and ET patients (regardless of mutational status) identified significant enrichment for genes in the tumor necrosis factor, NFκB, and MAPK pathways and upregulation of platelet proliferative drivers such as ITGA2B and ITGB3. Correlation with DNA methylation showed a consistent pattern of hypomethylation at upregulated gene promoters. Interrogation of these promoter regions highlighted enrichment of transcriptional regulators, which were significantly upregulated in patients with ET regardless of mutation status, including CEBPβ and NFκB. For "true" TN ET, patterns of gene expression and DNA methylation were similar to those in ET patients with known driver mutations. These observations suggest that the resultant ET phenotype may, at least in part and regardless of mutation type, be driven by transcriptional misregulation and may propagate downstream via the MAPK, tumor necrosis factor, and NFκB pathways with resultant JAK-STAT activation. These findings identify potential novel mechanisms of disease initiation that require further evaluation.

Indexed as

Thrombocythemia, EssentialCalreticulinHumansJanus Kinase 2Leukocytes, MononuclearReceptors, ThrombopoietinTranscriptomeCalreticulinJanus Kinase 2Receptors, Thrombopoietin

Identifiers

PMID33599741
PMCPMC7903233
OpenAlexW3130861925

What OpenQuestion 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 OpenQuestion graph.