Evidence map›Paper›PMID 20098702›Full record

ArticlePloS one2010

Molecular signatures of quiescent, mobilized and leukemia-initiating hematopoietic stem cells.

E Camilla Forsberg, Emmanuelle Passegué, Susan S Prohaska, Amy J Wagers, Martina Koeva, Joshua M Stuart, Irving L Weissman

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

75 citing papers in PubMed, 128 citations in OpenAlex.

  1. Heparan Sulfate Proteoglycans in Immunity.Proteoglycan research · 2026
    Article
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  4. Syndecans in hematopoietic cells and their niches.American journal of physiology. Cell physiology · 2024
    Review
  5. Article
  6. Review
  7. Cells · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. JAM-C/HemaSphere · 2021
    Article
  16. Article
  17. Article
  18. Article
  19. Safe and EffectiveHuman gene therapy · 2021
    Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 1 country.

E Camilla ForsbergInstitute for Biology of Stem Cells, Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, California, United States of America. cforsber@ucsc.edu
Emmanuelle Passegué
Susan S Prohaska
Amy J Wagers
Martina Koeva
Joshua M Stuart
Irving L Weissman
University of California, Santa Cruz · USStanford University · USJoslin Diabetes Center · USUniversity of California, San Francisco · US

Funding

STEM CELL DETRMINATION GENES IN HSC AND HEMATOLYMPHOID CELLS IN MICEP01DK053074 · NIDDK · STANFORD UNIVERSITY · PI CLARKE, MICHAEL F · 1997 to 2007
$8.3M
HSC Diversity: Regulation by Clonal Selection vs Epigenetic InductionR01CA086065 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2000 to 2017
$6.9M
MOLECULAR CHARACTERIZATION OF ACUTE MYELOID LEUKEMIAR01CA086017 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2000 to 2015
$5.5M
HOMING RECEPTOR DETERMINANTS ON HSCR01HL058770 · NHLBI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 1998 to 2013
$3.9M
The Role of JunB in Hematopoietic Stem Cell HomeostasisR01HL092471 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PASSEGUE, EMMANUELLE · 2008 to 2016
$3.6M
Control of HSC proliferation and migration by the transcription factor EGR1R01HL088582 · NHLBI · JOSLIN DIABETES CENTER · PI WAGERS, AMY JO · 2009 to 2013
$2.2M
NCI NIH HHS R01 CA086017NCI NIH HHS R01CA086017NCI NIH HHS R01 CA086065NCI NIH HHS R01CA086065NHLBI NIH HHS 1R01HL088582-01NHLBI NIH HHS 1R01HL092471-01NHLBI NIH HHS R01 HL058770NHLBI NIH HHS R01HL058770NHLBI NIH HHS R01 HL088582NHLBI NIH HHS R01 HL092471NIDDK NIH HHS P01 DK053074NIDDK NIH HHS P01DK053074
6 · The paper itself

Abstract

Hematopoietic stem cells (HSC) are rare, multipotent cells capable of generating all specialized cells of the blood system. Appropriate regulation of HSC quiescence is thought to be crucial to maintain their lifelong function; however, the molecular pathways controlling stem cell quiescence remain poorly characterized. Likewise, the molecular events driving leukemogenesis remain elusive. In this study, we compare the gene expression profiles of steady-state bone marrow HSC to non-self-renewing multipotent progenitors; to HSC treated with mobilizing drugs that expand the HSC pool and induce egress from the marrow; and to leukemic HSC in a mouse model of chronic myelogenous leukemia. By intersecting the resulting lists of differentially regulated genes we identify a subset of molecules that are downregulated in all three circumstances, and thus may be particularly important for the maintenance and function of normal, quiescent HSC. These results identify potential key regulators of HSC and give insights into the clinically important processes of HSC mobilization for transplantation and leukemic development from cancer stem cells.

Indexed as

AnimalsCell Transformation, NeoplasticDisease Models, AnimalFlow CytometryGene Expression ProfilingGene Expression RegulationHematopoietic Stem CellsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMiceMice, Inbred C57BLNucleic Acid HybridizationReverse Transcriptase Polymerase Chain ReactionTranscription, Genetic

Identifiers

PMID20098702
PMCPMC2808351
OpenAlexW2098528717

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.