Evidence map›Paper›PMID 20417684›Full record

ReviewExperimental hematology2010

Bone marrow stem cells and liver regeneration.

Graça Almeida-Porada, Esmail D Zanjani, Christopher D Porada

Abstract readReview
In one paragraph

Review in Experimental hematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Extracellular vesicles from bone marrow-derived mesenchymal stem cells protect against murine hepatic ischemia/reperfusion injury.Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society · 2017
    Article
  9. Review
  10. Review
  11. Article
  12. Could Stem Cell Therapy be the Cure in Liver Cirrhosis?Journal of clinical and experimental hepatology · 2015
    Review
  13. Article
  14. Are hematopoietic stem cells involved in hepatocarcinogenesis?Hepatobiliary surgery and nutrition · 2014
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

3 authors.

Graça Almeida-PoradaDepartment of Animal Biotechnology, University of Nevada, Reno, Reno, NV 89557-0104, USA. galmeida@cabnr.unr.edu
Esmail D Zanjani
Christopher D Porada

Funding

IN UTERO STEM CELL TRANSPLANTATIONR01HL052955 · NHLBI · UNIVERSITY OF NEVADA RENO · PI ZANJANI, ESMAIL · 1994 to 2011
$4.6M
In Utero Stem Cell Transplantation for Hemophilia AR01HL073737 · NHLBI · UNIVERSITY OF NEVADA RENO · PI ALMEIDA-PORADA, GRACA DUARTE · 2003 to 2006
$1.8M
Functional Analysis of the Hematopoietic Niche during OntogenyR01HL097623 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ALMEIDA-PORADA, GRACA DUARTE · 2009 to 2012
$1.4M
Evaluation of Stem Cell Plasticity In VivoR01HL070566 · NHLBI · UNIVERSITY OF NEVADA RENO · PI ALMEIDA-PORADA, GRACA DUARTE · 2001 to 2004
$866k
NHLBI NIH HHS HL52955NHLBI NIH HHS HL73737NHLBI NIH HHS HL97623NHLBI NIH HHS R01 HL052955NHLBI NIH HHS R01 HL070566NHLBI NIH HHS R01 HL073737NHLBI NIH HHS R01 HL097623
6 · The paper itself

Abstract

Development of new approaches to treat patients with hepatic diseases that can eliminate the need for liver transplantation is imperative. Use of cell therapy as a means of repopulating the liver has several advantages over whole-organ transplantation because it would be less invasive, less immunogenic, and would allow the use, in some instances, of autologous-derived cells. Stem/progenitor cells that would be ideal for liver repopulation would need to have characteristics such as availability and ease of isolation, the ability to be expanded in vitro, ensuring adequate numbers of cells, susceptibility to modification by viral vector transduction/genetic recombination, to correct any underlying genetic defects, and the ability of restoring liver function following transplantation. Bone marrow-derived stem cells, such as hematopoietic, mesenchymal and endothelial progenitor cells possess some or most of these characteristics, making them ideal candidates for liver regenerative therapies. Here, we will summarize the ability of each of these stem cell populations to give rise to functional hepatic elements that could mediate repair in patients with liver damage/disease.

Indexed as

Liver RegenerationStem Cell TransplantationBone Marrow CellsHumansLiver DiseasesStem Cells

Identifiers

PMID20417684
PMCPMC2882990

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.