Evidence map›Paper›PMID 25122688›Full record

ArticleStem cells translational medicine2014

Longitudinal Analysis of DNA Methylation in CD34+ Hematopoietic Progenitors in Myelodysplastic Syndrome.

Yan-Fung Wong, Chris N Micklem, Masataka Taguchi, Hidehiro Itonaga, Yasushi Sawayama, Daisuke Imanishi, Shinichi Nishikawa, Yasushi Miyazaki, Lars Martin Jakt

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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  4. Review
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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

9 authors at 4 institutions in 3 countries.

Yan-Fung WongLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan yan.fung.wong@sund.ku.dk mjakt@z2.keio.jp.
Chris N MicklemLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Masataka TaguchiLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Hidehiro ItonagaLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Yasushi SawayamaLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Daisuke ImanishiLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Shinichi NishikawaLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Yasushi MiyazakiLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan.
Lars Martin JaktLaboratory for Stem Cell Biology, RIKEN Center for Developmental Biology, Kobe, Japan; Department of Hematology, Atomic Bomb Disease and Hibakusya Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan; The Danish Stem Cell Centre (DanStem), University of Copenhagen, Copenhagen, Denmark; Imperial College London, London, United Kingdom; All About Science Japan, Kobe, Japan; Department of Systems Medicine, Mitsunada Sakaguchi Laboratory, Keio University School of Medicine, Institute of Integrated Medical Research, Tokyo, Japan yan.fung.wong@sund.ku.dk mjakt@z2.keio.jp.
Nagasaki University · JPImperial College London · GBKeio University · JPUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelodysplastic syndrome (MDS) is a disorder of hematopoietic stem cells (HSCs) that is often treated with DNA methyltransferase 1 (DNMT1) inhibitors (5-azacytidine [AZA], 5-aza-2'-deoxycytidine), suggesting a role for DNA methylation in disease progression. How DNMT inhibition retards disease progression and how DNA methylation contributes to MDS remain unclear. We analyzed global DNA methylation in purified CD34+ hematopoietic progenitors from MDS patients undergoing multiple rounds of AZA treatment. Differential methylation between MDS phenotypes was observed primarily at developmental regulators not expressed within the hematopoietic compartment and was distinct from that observed between healthy hematopoietic cell types. After AZA treatment, we observed only limited DNA demethylation at sites that varied between patients. This suggests that a subset of the stem cell population is resistant to AZA and provides a basis for disease relapse. Using gene expression data from patient samples and an in vitro AZA treatment study, we identified differentially methylated genes that can be activated following treatment and that remain silent in the CD34+ stem cell compartment of high-risk MDS patients. Haploinsufficiency in mice of one of these genes (NR4A2) has been shown to lead to excessive HSC proliferation, and our data suggest that suppression of NR4A2 by DNA methylation may be involved in MDS progression.

Indexed as

Antigens, CD34AzacitidineDNA MethylationEnzyme InhibitorsHematopoietic Stem CellsHumansLongitudinal StudiesMyelodysplastic SyndromesPolymerase Chain ReactionTranscriptomeAntigens, CD34AzacitidineEnzyme InhibitorsAzacytidineDNA methylationMDSMyelodysplastic syndromes

Identifiers

PMID25122688
PMCPMC4181398
OpenAlexW2027060031

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.