Evidence map›Paper›PMID 23372166›Full record

ArticleBlood2013

RUNX1a enhances hematopoietic lineage commitment from human embryonic stem cells and inducible pluripotent stem cells.

Dan Ran, Wei-Jong Shia, Miao-Chia Lo, Jun-Bao Fan, David A Knorr, Patrick I Ferrell, Zhaohui Ye, Ming Yan, Linzhao Cheng, Dan S Kaufman and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
  2. Blood Pharming of Red Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
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  18. Article
  19. Role of GATA2 in Human NK Cell Development.Critical reviews in immunology · 2021
    Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Dan RanMoores University of California at San Diego Cancer Center, University of California at San Diego, La Jolla, CA, USA.
Wei-Jong Shia
Miao-Chia Lo
Jun-Bao Fan
David A Knorr
Patrick I Ferrell
Zhaohui Ye
Ming Yan
Linzhao Cheng
Dan S Kaufman
Dong-Er Zhang
University of California, San Diego · USUniversity of Minnesota · USJohns Hopkins Medicine · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008244 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SHIMIZU, YOJI · 1988 to 2024
$13.6M
Stem Cell Therapy for Myocardial RepairR01HL067828 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI KAUFMAN, DAN S., ZHANG, JIANYI · 2001 to 2014
$4.7M
Human embryonic stem (ES) and embroyonic germ (EG) cells to blood and immune cellR01HL073781 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CHENG, LINZHAO · 2003 to 2013
$4.2M
DEVELOPMENTAL BIOLOGY TRAINING PROGRAMT32HD007480 · NICHD · UNIVERSITY OF MINNESOTA TWIN CITIES · PI O'CONNOR, MICHAEL BRENDAN · 1995 to 2011
$1.2M
Stem Cell Biology Training ProgramT32HD060536 · NICHD · UNIVERSITY OF MINNESOTA · PI KAUFMAN, DAN S. · 2010 to 2014
$779k
SYNTHESIS AND EVALUATION OF POTENTIAL ENAMINONE AND SPIROIMIDOOXY ANTICONVULSANTSS06GM008244 · NIGMS · HOWARD UNIVERSITY · PI TOUSSAINT, ROSE-MARIE · 1989 to 1998
–
NHLBI NIH HHS R01 HL067828NHLBI NIH HHS R01-HL067828NHLBI NIH HHS R01 HL073781NHLBI NIH HHS R01-HL073781NICHD NIH HHS 5T32HD007480NICHD NIH HHS T32 HD007480NICHD NIH HHS T32 HD060536NICHD NIH HHS T32HD060536NIGMS NIH HHS S06 GM008244NIGMS NIH HHS T32 GM008244
6 · The paper itself

Abstract

Advancements in human pluripotent stem cell (hPSC) research have potential to revolutionize therapeutic transplantation. It has been demonstrated that transcription factors may play key roles in regulating maintenance, expansion, and differentiation of hPSCs. In addition to its regulatory functions in hematopoiesis and blood-related disorders, the transcription factor RUNX1 is also required for the formation of definitive blood stem cells. In this study, we demonstrated that expression of endogenous RUNX1a, an isoform of RUNX1, parallels with lineage commitment and hematopoietic emergence from hPSCs, including both human embryonic stem cells and inducible pluripotent stem cells. In a defined hematopoietic differentiation system, ectopic expression of RUNX1a facilitates emergence of hematopoietic progenitor cells (HPCs) and positively regulates expression of mesoderm and hematopoietic differentiation-related factors, including Brachyury, KDR, SCL, GATA2, and PU.1. HPCs derived from RUNX1a hPSCs show enhanced expansion ability, and the ex vivo-expanded cells are capable of differentiating into multiple lineages. Expression of RUNX1a in embryoid bodies (EBs) promotes definitive hematopoiesis that generates erythrocytes with β-globin production. Moreover, HPCs generated from RUNX1a EBs possess ≥9-week repopulation ability and show multilineage hematopoietic reconstitution in vivo. Together, our results suggest that RUNX1a facilitates the process of producing therapeutic HPCs from hPSCs.

Indexed as

Blotting, WesternBrachyury ProteinCell DifferentiationCell LineCell LineageCell ProliferationCells, CulturedCore Binding Factor Alpha 2 SubunitEmbryoid BodiesEmbryonic Stem CellsFetal ProteinsGATA2 Transcription FactorGene ExpressionHematopoietic Stem CellsHumansInduced Pluripotent Stem CellsBrachyury ProteinCore Binding Factor Alpha 2 SubunitFetal ProteinsGATA2 protein, humanGATA2 Transcription FactorProto-Oncogene ProteinsProto-Oncogene Protein Spi-1RUNX1 protein, humanT-Box Domain ProteinsTrans-Activators

Identifiers

PMID23372166
PMCPMC3624936
OpenAlexW2064813555

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.