Evidence map›Paper›PMID 28375987›Full record

ReviewCurrent opinion in hematology2017

Hematopoietic stem cells under pressure.

Miguel Ganuza, Shannon McKinney-Freeman

Abstract readReview
In one paragraph

Review in Current opinion in hematology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. The evolving hematopoietic niche during development.Frontiers in molecular biosciences · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Role ofFrontiers in cell and developmental biology · 2021
    Review
  18. Connecting secretome to hematopoietic stem cell phenotype shifts in an engineered bone marrow niche.Integrative biology : quantitative biosciences from nano to macro · 2020
    Article
  19. Review
  20. 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

2 authors at 2 institutions in 1 country.

Miguel GanuzaDepartment of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Shannon McKinney-Freeman
St. Jude Children's Research Hospital · USUniversity of Tennessee Health Science Center · US

Funding

Defining Nfix's role as a novel key regulator of hematopoietic stem cellsR01DK104028 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNEY-FREEMAN, SHANNON L · 2016 to 2020
$2.0M
Characterization of embryonic stem cell-derived hematopoietic stem cellsK01DK080846 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNEY-FREEMAN, SHANNON L · 2008 to 2012
$771k
Functional study of novel transcriptional regulators of hematopoietic stem cellsR03DK093731 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI MCKINNEY-FREEMAN, SHANNON L · 2012 to 2012
$88k
NIDDK NIH HHS K01 DK080846NIDDK NIH HHS R01 DK104028NIDDK NIH HHS R03 DK093731
6 · The paper itself

Abstract

purpose of reviewHematopoietic stem cells (HSCs) and progenitors are tasked with maintaining hematopoietic homeostasis in the face of numerous insults and challenges, including infection, inflammation, and exsanguination. HSCs possess the remarkable ability to reconstitute the entire hematopoietic system of an organism whose own hematopoietic system has been ablated. This ability is exploited routinely in the clinic via HSC transplantation (HSCT). Here, we focus on the physiological and molecular bottlenecks overcome by HSCs during transplantation. RECENT

findingsDuring transplantation, HSCs encounter a damaged bone marrow niche, characterized molecularly by increases in oxygen concentrations and an altered cytokine milieu. New mechanisms and pathways have been recently implicated during HSCT, including transplanted HSC-dependent secretion of conditioning molecules that facilitate engraftment and pathways that protect HSCs from perturbed organelle homeostasis. SUMMARY: Better understanding the molecular processes HSCs employ to withstand the stress of transplant will illuminate novel targets for further improving conditioning regimens and engraftment during HSCT.

Indexed as

Stress, PhysiologicalAnimalsCell MovementEpigenesis, GeneticGene Expression RegulationGraft SurvivalHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHomeostasisHumansOrganellesOxidative StressReactive Oxygen SpeciesStem Cell NicheTransplantation ConditioningReactive Oxygen Species

Identifiers

PMID28375987
PMCPMC5669070
OpenAlexW2602614440

What OpenQuestion holds

Textmetadata
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.