Evidence map›Paper›PMID 32823933›Full record

ReviewCells2020

MPN: The Molecular Drivers of Disease Initiation, Progression and Transformation and their Effect on Treatment.

Julian Grabek, Jasmin Straube, Megan Bywater, Steven W Lane

Abstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

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  11. bioRxiv : the preprint server for biology · 2025
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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

4 authors.

Julian GrabekCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.ORCID 0000-0001-5168-050X
Jasmin StraubeCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
Megan BywaterCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
Steven W LaneCancer Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloproliferative neoplasms (MPNs) constitute a group of disorders identified by an overproduction of cells derived from myeloid lineage. The majority of MPNs have an identifiable driver mutation responsible for cytokine-independent proliferative signalling. The acquisition of coexisting mutations in chromatin modifiers, spliceosome complex components, DNA methylation modifiers, tumour suppressors and transcriptional regulators have been identified as major pathways for disease progression and leukemic transformation. They also confer different sensitivities to therapeutic options. This review will explore the molecular basis of MPN pathogenesis and specifically examine the impact of coexisting mutations on disease biology and therapeutic options.

Indexed as

Disease ProgressionMutationAnimalsBone Marrow TransplantationHumansImmune Checkpoint InhibitorsMiceMyeloproliferative DisordersPhenotypePrognosisTransplantation, HomologousImmune Checkpoint InhibitorsCALRchromatin modifiersDNA methylationdriver mutationsIFNαJAK2leukemic transformationMPLMPNmyeloproliferationspliceosometranscriptional regulatorstumour suppressors

Identifiers

PMID32823933
PMCPMC7465511

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.