Evidence map›Paper›PMID 20828588›Full record

ReviewAdvanced drug delivery reviews2010

Mesenchymal stem cells as therapeutics and vehicles for gene and drug delivery.

Christopher D Porada, Graça Almeida-Porada

Open access · greenAbstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed, 1 pooled it
6.8field-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

88 citing papers in PubMed, 1 synthesis or guideline pooled it, 230 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
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  7. Review
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  11. Article
  12. Biology and Therapeutic Properties of Mesenchymal Stem Cells in Leukemia.International journal of molecular sciences · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Interleukin gene delivery for cancer gene therapy:Iranian journal of basic medical sciences · 2023
    Review
  20. Review

28 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

2 authors at 1 institution in 1 country.

Christopher D PoradaDepartment of Animal Biotechnology, University of Nevada, Reno, 89557-0104, USA. cporada@cabnr.unr.edu
Graça Almeida-Porada
University of Nevada, Reno · US

Funding

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
In Utero Gene TherapyR01HD043038 · NICHD · UNIVERSITY OF NEVADA RENO · PI PORADA, CHRISTOPHER D · 2002 to 2006
$997k
Evaluation of Stem Cell Plasticity In VivoR01HL070566 · NHLBI · UNIVERSITY OF NEVADA RENO · PI ALMEIDA-PORADA, GRACA DUARTE · 2001 to 2004
$866k
NHLBI NIH HHS R01 HL070566NHLBI NIH HHS R01 HL073737NHLBI NIH HHS R01 HL097623NICHD NIH HHS R01 HD043038
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) possess a set of several fairly unique properties which make them ideally suited both for cellular therapies/regenerative medicine, and as vehicles for gene and drug delivery. These include: 1) relative ease of isolation; 2) the ability to differentiate into a wide variety of seemingly functional cell types of both mesenchymal and non-mesenchymal origin; 3) the ability to be extensively expanded in culture without a loss of differentiative capacity; 4) they are not only hypoimmunogenic, but they produce immunosuppression upon transplantation; 5) their pronounced anti-inflammatory properties; and 6) their ability to home to damaged tissues, tumors, and metastases following in vivo administration. In this review, we summarize the latest research in the use of mesenchymal stem cells in regenerative medicine, as immunomodulatory/anti-inflammatory agents, and as vehicles for transferring both therapeutic genes in genetic disease and genes designed to destroy malignant cells.

Indexed as

Drug Delivery SystemsGenetic TherapyImmunomodulationMesenchymal Stem CellsCell DifferentiationCell ProliferationGenetic VectorsHumansImmune ToleranceImmunosuppression TherapyMesenchymal Stem Cell TransplantationNeoplasmsTissue Engineering

Identifiers

PMID20828588
PMCPMC2991625
OpenAlexW1980039759

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.