Evidence map›Paper›PMID 26049752›Full record

ReviewCurrent opinion in hematology2015

Progress and obstacles towards generating hematopoietic stem cells from pluripotent stem cells.

Jungmin Lee, Brad Dykstra, Robert Sackstein, Derrick J Rossi

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Long-Term Engraftment and Fetal Globin Induction uponMolecular therapy. Methods & clinical development · 2017
    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

4 authors at 2 institutions in 1 country.

Jungmin LeeaDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge bProgram in Cellular and Molecular Medicine, Division of Hematology/Oncology, Boston Children's Hospital cDepartment of Dermatology, and Program of Excellence in Glycosciences, Brigham & Women's Hospital, Harvard Medical School dDivision of Hematology, Department of Medicine, Brigham & Women's Hospital eDepartment of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston fHarvard Stem Cell Institute, Cambridge, Massachusetts, USA *Jungmin Lee and Brad Dykstra contributed equally to the writing of this manuscript.
Brad Dykstra
Robert Sackstein
Derrick J Rossi
Harvard University · USGTx (United States) · US

Funding

Coordinating Center for Beta Cell Biology ConsortiumU01DK072473 · NIDDK · VANDERBILT UNIVERSITY · PI MAGNUSON, MARK A · 2005 to 2014
$61.0M
REGULATION OF LACTOSAMINYL GLYCAN BIOSYNTHESIS IN HEMATOPOIETIC CELLSP01HL107146 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKSTEIN, ROBERT · 2011 to 2017
$17.7M
Reprogramming committed blood cells to a hematopoietic stem cell fateR01HL107630 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI ROSSI, DERRICK J. · 2011 to 2015
$2.5M
NHLBI NIH HHS P01 HL107146NHLBI NIH HHS R01 HL107630NHLBI NIH HHS R01HL107630NIDDK NIH HHS U01 DK072473NIDDK NIH HHS U01DK072473
6 · The paper itself

Abstract

purpose of reviewHuman pluripotent stem cells (PSCs) have the potential to provide an inexhaustible source of hematopoietic stem cells (HSCs) that could be used in disease modeling and in clinical applications such as transplantation. Although the goal of deriving definitive HSCs from PSCs has not been achieved, recent studies indicate that progress is being made. This review will provide information on the current status of deriving HSCs from PSCs, and will highlight existing challenges and obstacles. RECENT

findingsRecent strides in HSC generation from PSCs has included derivation of developmental intermediates, identification of transcription factors and small molecules that support hematopoietic derivation, and the development of strategies to recapitulate niche-like conditions. SUMMARY: Despite considerable progress in defining the molecular events driving derivation of hematopoietic progenitor cells from PSCs, the generation of robust transplantable HSCs from PSCs remains elusive. We propose that this goal can be facilitated by better understanding of the regulatory pathways governing HSC identity, development of HSC supportive conditions, and examining the marrow homing properties of PSC-derived HSCs.

Indexed as

Cell- and Tissue-Based TherapyCell DifferentiationCell LineageCell MovementHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansPluripotent Stem CellsSmall Molecule LibrariesStem Cell NicheTranscription FactorsSmall Molecule LibrariesTranscription Factors

Identifiers

PMID26049752
PMCPMC4459525
OpenAlexW623099452

What OpenQuestion holds

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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.