Evidence map›Paper›PMID 38177095›Full record

ArticleBlood cancer journal2024

Genomic and functional impact of Trp53 inactivation in JAK2V617F myeloproliferative neoplasms.

Panhong Gou, Duanya Liu, Saravanan Ganesan, Evelyne Lauret, Nabih Maslah, Veronique Parietti, Wenchao Zhang, Véronique Meignin, Jean-Jacques Kiladjian, Bruno Cassinat and 1 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Unraveling the role ofHemaSphere · 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

11 authors at 3 institutions in 1 country.

Panhong GouInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.ORCID 0000-0001-9408-5663
Duanya LiuInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.
Saravanan GanesanInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.
Evelyne LauretUniversité de Paris, Institut Cochin, Inserm U1016, CNRS UMR 8104, Paris, France.
Nabih MaslahInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.ORCID 0000-0002-5553-462X
Veronique PariettiUniversité de Paris Cité, Paris, France.
Wenchao ZhangUniversité de Paris Cité, Paris, France.
Véronique MeigninUniversité de Paris Cité, Paris, France.
Jean-Jacques KiladjianInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.
Bruno CassinatInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France.ORCID 0000-0002-6514-3905
Stephane GiraudierInserm UMR-S 1131, Hôpital Saint-Louis, Paris, France. stephane.giraudier@aphp.fr.ORCID 0000-0002-1817-2236
Inserm · FRCentre National de la Recherche Scientifique · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical myeloproliferative neoplasms (MPNs) are characterized by the proliferation of myeloid cells and the risk of transformation into myelofibrosis or acute myeloid leukemia (AML) and TP53 mutations in MPN patients are linked to AML. However, JAK2V617F has been reported to impact the TP53 response to DNA damage, suggesting potential overlapping role of TP53 inactivation in MPN. We established a mouse model showing that JAK2V617F/Vav-Cre/Trp53

Indexed as

Leukemia, Myeloid, AcuteMyeloproliferative DisordersAnimalsGenomicsHumansInterferon-alphaJanus Kinase 2MiceMutationTumor Suppressor Protein p53Interferon-alphaJanus Kinase 2Tumor Suppressor Protein p53

Identifiers

PMID38177095
PMCPMC10766605
OpenAlexW4390585893

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.