Evidence map›Paper›PMID 26147687›Full record

ArticleNature immunology2015

The transcription factor Foxm1 is essential for the quiescence and maintenance of hematopoietic stem cells.

Yu Hou, Wen Li, Yue Sheng, Liping Li, Yong Huang, Zhonghui Zhang, Tongyu Zhu, David Peace, John G Quigley, Wenshu Wu and 2 more

Abstract read
In one paragraph

Article in Nature immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

54 citing papers in PubMed, 76 citations in OpenAlex.

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  15. mHaematologica · 2022
    Article
  16. Article
  17. Article
  18. ATR activity controls stem cell quiescence via the cyclin F-SCF complex.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. Article
  20. Molecular regulation of hematopoietic stem cell quiescence.Cellular and molecular life sciences : CMLS · 2022
    Review
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

12 authors at 4 institutions in 2 countries.

Yu HouDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Wen LiDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Yue ShengDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Liping Li1] Department of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA. [2] Fudan University ZhongShan Hospital, Shanghai, China.
Yong HuangSection of Gastroenterology, Department of Medicine, The University of Chicago, Chicago, Illinois, USA.
Zhonghui ZhangDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Tongyu ZhuFudan University ZhongShan Hospital, Shanghai, China.
David PeaceDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
John G QuigleyDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Wenshu WuDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
You-Yang ZhaoDepartment of Pharmocology, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
Zhijian QianDepartment of Medicine and Cancer Research Center, The University of Illinois Hospital and Health Sciences System, Chicago, Illinois, USA.
University of Illinois Chicago · USUniversity of Illinois Hospital & Health Sciences System · USFudan University · CNUniversity of Chicago · US

Funding

Trpm2 Regulation of Phagocyte Bactericidal Activity and Resolution of Lung InjuryP01HL077806 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B. · 2005 to 2019
$27.0M
Repair mechanisms of sepsis induced endothelial dysfunction and lung injuryR01HL125350 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B., ZHAO, YOU-YANG · 2014 to 2018
$3.2M
Novel Signalings and Molecular Targets Of Endothelial Regeneration In Aging LungR01HL123957 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ZHAO, YOU-YANG · 2014 to 2018
$2.0M
The Role of the APC Tumor Suppressor Gene in Hematopoiesis and LeukemogenesisR01CA140979 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI QIAN, ZHIJIAN · 2010 to 2014
$1.6M
NCI NIH HHS R01 CA140979NHLBI NIH HHS P01 HL077806NHLBI NIH HHS R01 HL123957NHLBI NIH HHS R01 HL125350
6 · The paper itself

Abstract

Foxm1 is known as a typical proliferation-associated transcription factor. Here we found that Foxm1 was essential for maintenance of the quiescence and self-renewal capacity of hematopoietic stem cells (HSCs) in vivo in mice. Reducing expression of FOXM1 also decreased the quiescence of human CD34(+) HSCs and progenitor cells, and its downregulation was associated with a subset of myelodysplastic syndrome (MDS). Mechanistically, Foxm1 directly bound to the promoter region of the gene encoding the receptor Nurr1 (Nr4a2; called 'Nurr1' here), inducing transcription, while forced expression of Nurr1 reversed the loss of quiescence observed in Foxm1-deficient cells in vivo. Thus, our studies reveal a previously unrecognized role for Foxm1 as a critical regulator of the quiescence and self-renewal of HSCs mediated at least in part by control of Nurr1 expression.

Indexed as

Gene Expression RegulationAnimalsCell ProliferationCells, CulturedFlow CytometryForkhead Box Protein M1Forkhead Transcription FactorsGene Expression ProfilingHEK293 CellsHematopoietic Stem CellsHumansMice, Inbred C57BLMice, KnockoutMice, TransgenicMyelodysplastic SyndromesNuclear Receptor Subfamily 4, Group A, Member 2Forkhead Box Protein M1Forkhead Transcription FactorsFOXM1 protein, humanFoxm1 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 2

Identifiers

PMID26147687
PMCPMC4509925
OpenAlexW1513310554

What OpenQuestion holds

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LicenceTDM
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.