Evidence map›Paper›PMID 38067298›Full record

ArticleCancers2023

Development of MDS in Pediatric Patients with GATA2 Deficiency: Increased Histone Trimethylation and Deregulated Apoptosis as Potential Drivers of Transformation.

Franziska Schreiber, Guido Piontek, Yuki Schneider-Kimoto, Stephan Schwarz-Furlan, Rita De Vito, Franco Locatelli, Carole Gengler, Ayami Yoshimi, Andreas Jung, Frederick Klauschen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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

13 authors at 7 institutions in 3 countries.

Franziska SchreiberInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Guido PiontekInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Yuki Schneider-KimotoInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Stephan Schwarz-FurlanInstitute of Pathology, Klinikum Kaufbeuren-Ravensburg, 87600 Kaufbeuren, Germany.
Rita De VitoDepartment of Pathology, Bambino Gesu Children's Hospital, IRCCS, 00165 Rome, Italy.
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Cell and Gene Therapy, Bambino Gesu Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0002-7976-3654
Carole GenglerInstitute of Pathology, Department of Laboratory Medicine and Pathology, Lausanne University Hospital, Lausanne University, CH-1011 Lausanne, Switzerland.
Ayami YoshimiDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, 79110 Freiburg, Germany.
Andreas JungInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Frederick KlauschenInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Charlotte M NiemeyerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, 79110 Freiburg, Germany.ORCID 0000-0003-3856-7937
Miriam ErlacherDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, 79110 Freiburg, Germany.
Martina RudeliusInstitute of Pathology, Ludwig-Maximilians-University Munich, 80337 Munich, Germany.
Ludwig-Maximilians-Universität München · DEUniversity of Freiburg · DEBambino Gesù Children's Hospital · ITGerman Cancer Research Center · DEUniversità Cattolica del Sacro Cuore · ITUniversitätsklinikum Erlangen · DEUniversity of Lausanne · CH

Funding

Deutsche José Carreras Leukämie-Stiftung DJCLS 10R/2020Federal Ministry of Education and Research no 01GM1911A and 01GM2207A
6 · The paper itself

Abstract

GATA2 deficiency is a heterogeneous, multisystem disorder associated with a high risk of developing myelodysplastic syndrome (MDS) and the progression to acute myeloid leukemia. The mechanisms underlying malignant transformation in GATA2 deficiency remain poorly understood, necessitating predictive markers to assess an individual's risk of progression and guide therapeutic decisions. In this study, we performed a systematic analysis of bone marrow biopsies from 57 pediatric MDS patients. Focusing on hematopoiesis and the hematopoietic niche, including its microenvironment, we used multiplex immunofluorescence combined with multispectral imaging, gene expression profiling, and multiplex RNA in situ hybridization. Patients with a GATA2 deficiency exhibited a dysregulated

Indexed as

apoptosischildhoodGATA2 deficiencymyelodysplastic syndromepediatric

Identifiers

PMID38067298
PMCPMC10705137
OpenAlexW4389056113

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.